DDO: a diabetes mellitus diagnosis ontology
© The Author(s) 2016
Received: 8 March 2016
Accepted: 15 August 2016
Published: 25 August 2016
Diabetes mellitus is a major cause of morbidity and mortality in humans. Early diagnosis is the first step toward the management of this condition. However, a diagnosis involves several variables, which makes it difficult to arrive at an accurate and timely diagnosis and to construct accurate personalized treatment plans. An electronic health record system requires an integrated decision support capability, and ontologies are rapidly becoming necessary for the design of efficient, reliable, extendable, reusable, and semantically intelligent knowledge bases. In this study, we take the first step in this direction, by designing an OWL2 diabetes diagnosis ontology (DDO). Protégé 5 software was used for the construction of the ontology. DDO is developed within the framework of the basic formal ontology and the ontology for general medical science to represent entities in the domain of diabetes, and it follows the design principles recommended by the Open Biomedical Ontology Foundry. Currently, DDO contains 6444 concepts, 48 properties, 13,551 annotations, and 27,127 axioms. DDO can serve as a diabetes knowledge base and supports automatic reasoning. It represents a major step toward the development of a new generation of patient-centric decision support tools. DDO is available through BioPortal at: http://www.bioportal.bioontology.org/ontologies/DDO.
Diabetes mellitus (DM) encompasses a group of metabolic disorders characterized by a chronic hyperglycemic condition, resulting from defects in insulin secretion, insulin action, or both. It is predicted that it will be the seventh leading cause of death by 2030.1 According to the International Diabetes Federation (IDF),2 387 million people worldwide were living with DM in 2014. This number is expected to increase to over 592 million (~10 % of the world’s population) by 2035. Undiagnosed cases of DM are thought to reach up to 179 million (Zarkogianni et al. 2015), and 4.9 million deaths were attributed to DM in 2014. In addition to the financial burden of diabetes, diabetes is associated with an increased risk of morbidity and mortality. The American Diabetes Association (Anyanwagu et al. 2015) categorizes diabetes into two main types: type-I and type-II. Type-I accounts for 10 % of diabetics. This type is usually diagnosed in children and young adults. Type-II accounts for the remaining 90 % of diabetics.
Diabetes remains a public health problem, despite the availability of several clinical practice guidelines CPGs, research studies, and medications (Zarkogianni et al. 2015). The adherence to large text-based CPGs, even those that are broadly acceptable, is often low. The excessive and increasing number of guidelines makes it hard for physicians to recall, locate, and appropriately apply them. Diagnosis of diabetes is the first and most important step for its prevention, detection, and management (Zarkogianni et al. 2015). Diagnosis describes the process of identifying the syndrome or disease affecting a patient (Bickley and Szilagyi 2012). Bickley and Szilagyi (2012) asserted that for diagnosis, physicians must first gather the indications of a disease, including the past medical history of a patient, symptoms, family history, and physical examinations. Finally, complementary explorations, such as laboratory tests, can increase or decrease the likelihood of a diagnosis. Regarding diabetes, some laboratory tests, such as HbA1c, FPG, BMI, or OGTT, are generally appropriate for directly screening diabetes or pre-diabetes (Anyanwagu et al. 2015). However, such methods can be limited and may be inadequate for detecting high-risk individuals (Buysschaert et al. 2015). For example, HbA1c measurements may be altered in the setting of anemia or renal failure, and HbA1c may remain in the normal range for some patients with mild dysglycemia.
Owing to the asymptomatic nature of the DM disease at the early stage, the patient can be affected by it for 9–12 years prior to being diagnosed (Tripathi and Srivastava 2006; Zarkogianni et al. 2015). At the same time, diabetic retinopathy occurs in three quarters of all people that have diabetes for 15 years, and is the most common cause of blindness. Approximately half of all people with diabetes exhibit some degree of neuropathy (Tripathi and Srivastava 2006). In addition, high urine glucose predisposes patients to urinary tract infections (UTI). As many as 25 % of individuals that are newly diagnosed with diabetes exhibit diabetic retinopathy or microalbuminuria, suggesting that there is an average 7-year gap between the actual onset and the diagnosis of diabetes (Buysschaert et al. 2015). Buysschaert et al. (2015) surveyed the association between diabetes and other complications. As a result, acute and chronic complications are often present at the time of diagnosis (Tripathi and Srivastava 2006; Anyanwagu et al. 2015; Buysschaert et al. 2015).
The diagnosing of diabetes can be affected by other factors, which can confirm whether diabetes is present regardless of whether laboratory test results are in normal or abnormal ranges (Chen et al. 2012). Some examples of these factors are as follows (Buysschaert et al. 2015): (1) The patient’s current complications that are related to diabetes such as microvascular diseases (e.g., retinopathy, nephropathy, neuropathy), macrovascular diseases (e.g., cerebrovascular, peripheral vascular, coronary artery,), and infections and other complications (e.g., psychosocial problems, dental disease, nonalcoholic fatty liver disease (NAFLD), dyslipidemia). For example, Ortiz-Lopez et al. (2012) suggested the usage of NAFLD as a predictor of type-II diabetes. (2) Medications affecting glucose levels such as prednisone, olanzapine, glucocorticoids, chemotherapy agents, antipsychotics, and mood stabilizers. (3) Demographic factors such as gender, age, whether the patient is a smoker, and race. (4) Symptoms such as polydipsia, polyphagia, vision, and polyuria (U.S. Department of Health and Human Services 2016; American Diabetes Association 2016; Canadian Diabetes Association 2016; National Institute for Health and Care Excellence (NICE) 2016). For example, the American Diabetes Association (ADA) (Anyanwagu et al. 2015) confirmed that the diagnosis of type-II diabetes (T2DM) involves the testing of signs or conditions associated with insulin resistance (e.g., acanthosis nigricans; hypertension; dyslipidemia; polycystic ovarian syndrome; small-for-gestational-age birth weight; or cancer in the liver, pancreas, endometrium, colon/rectum, breast, or bladder). The ADA also confirmed an association between fasting plasma glucose (FPG) results and the presence of retinopathy. The Canadian Diabetes Association (CDA) asserted that the HbA1c laboratory test is affected by many disorders such as hyperbilirubinemia, hypertriglyceridemia, chronic renal failure, chronic liver disease, and hemoglobinopathies. Moreover, some laboratory tests are not compatible with some complications. For example, HbA1c cannot be used for screening patients with homozygous hemoglobinopathies, anemia, EPO therapy, treatments of cancer, hepatitis C, and sever hyperlipidemia.
Many diabetes symptoms are indications of other diseases, such as obesity, which is a major risk factor for DM and cardiovascular diseases (CVD). Tumor markers are used to diagnose pancreatic cancer, but are also an indicator of pancreatic tissue damage, which can be caused by diabetes. In addition, the identified complications that are associated with diabetes help with the creation of a comprehensive care plan for diabetes, containing medication, physical activity, education, and diet programs. There are approximately 100 main complications associated with DM. In 2013, Liu et al. (2013) mined the top 10 complications. Moreover, drugs may induce hyperglycemia through a variety of mechanisms, including alterations in insulin secretion and sensitivity, direct cytotoxic effects on pancreatic cells, and increases in glucose production. These drugs include statins (e.g., fluvastatin, lovastatin, and pravastatin), antibiotics (Fluoroquinolones), atorvastatin (Lipitor), rosuvastatin (Crestor), simvastatin (Zocor), and chemotherapeutic agents (Anyanwagu et al. 2015). However, statins are the most widely prescribed medications for the prevention of cardiovascular events.
Unacceptable morbidity and mortality rates are still recorded in all countries. The effectiveness of the therapy for a disease depends mainly on the level of accuracy and the timing of its diagnosis. The complexities present practicing medicine make conventional quantitative diagnosis approaches inadequate, and hence new techniques are required. In developing countries, such as Egypt, where a population explosion presents a major concern, maintaining manual screening systems for DM patients throughout the country is not an easy task (Yao and Kumar 2013). A system or search engine is required that is able to both detect asymptomatic DM cases in their early stages by using electronic health records (EHR) and support physicians at the point of care for diagnosing specific cases. Clinical decision support systems (CDSS) play a key role in the search for success in the domain of diabetes (Sanchez et al. 2013; Miller et al. 2015). To be effective, CDSS must be proactive, and provide physicians with the right knowledge, in the right form, at the right time (Schreiber 2000).
As previously asserted, the diagnosis of DM diagnosis requires many features. If CDSS is designed as a standalone system, then physicians must enter these features for each patient. This is not feasible, as it would interrupt the clinical workflow of physicians. The solution for this problem is to integrate CDSS as a component of the EHR system (Ahmadian et al. 2010). As a result, CDSS can automatically collect a patient’s features from their profile, even from a distributed environment. However, some issues can prevent advanced data exchange and integration in an EHR environment, including the frequent usage of diverse terminologies to represent the same concept, a lack of logical and machine-readable relationships between different terms, and the lack of a machine-readable and community supported data exchange format (e.g., the OWL format) for the representation of medical data. These obstacles are an obstacle to computer-assisted automated reasoning.
The automation of data collection requires the standardization of the applicable terminology, in order to solve the interoperability and portability problems (Ahmadian et al. 2010). If we treat the categorical features, such as a patient’s current medications, diseases, and symptoms, as regular categorical features, then we will lose the associated semantics. For example, if the patient has hypertension, which can affect the decision of a physician regarding a DM diagnosis, the disease may be not stored in EHR under this name. Hypertension has many synonyms and related sub-diseases. For example, for SNOMED CT (SCT)3 there are 178 other diseases, such as “eclampsia,” which are considered as being related to or subtypes of hypertension. String similarity is not suitable for verifying the clinical relationship between these concepts (Agrawal and Elhanan 2014). When CDSS collects a patient’s features, it must detect such semantic relationships between the collected diseases, symptoms, and medications in order to mimic the reasoning of doctors. The best solution for handling this challenge is to bind CDSS with ontologies (Gruber 1995; Chen et al. 2012; Sanchez et al. 2013; Rahimi et al. 2014).
Ontologies play an important role in areas such as knowledge management; data integration, exchange, and semantic interoperability; and decision support and reasoning (Button et al. 2013; Suzuki et al. 2015; Mugzach et al. 2015). Ontology can preserve the semantic relationships between its concepts, and hence improve the intelligence of decision support systems. Many CPG languages, such as GLIF, EON, GEM, and Asbru, have exploited this idea to solve the curly braces problem in the Arden syntax language (Ahmadian et al. 2010). Hsu et al. (2015) enhanced the common observational medical outcomes partnership (OMOP)4 data model by linking its fields with an ontology for an intracranial aneurysm. As a result, they were able to support semantic queries over EHR data. Building ontologies based on existing standard medical ontologies or terminologies, such as SCT, gene ontology (GO), UMLS,5 and RxNorm, can further improve the interoperability between CDSS and an EHR environment (Agrawal and Elhanan 2014).
The project described in this paper represents the first step toward a comprehensive research program to develop and evaluate new generation informatics interventions for facilitating problem-solving in diabetes management. The first step of this research is to develop a formal organization system of diabetes-specific diagnosis knowledge by using ontology, and to validate this knowledge base for accuracy, completeness, appropriateness, and clarity. We propose Diabetes Mellitus Diagnosis Ontology (DDO), which will be encoded in the OWL 2 format by using the Protégé 5 tool. The core of DDO is developed within the framework of the basic formal ontology (BFO)6 (Arp et al. 2015) and the ontology for general medical sciences (OGMS)7 (Richard et al. 2009). The ontology concepts are collected from existing standard ontologies, including disease ontology (DOID) (Schrim and Mitraka 2015), symptom ontology (SYMP), RxNorm ontology, SCT terminology, UMLS, units of measurements (UO),8 and other OBO ontologies (BioPortal repository 2016). The remainder of this paper is organized as follows. “Related work” section describes related work. “Methods” section discusses the methodology for creating DDO. “Results and discussion” section presents our results and a discussion regarding them. Finally, “Conclusion” section presents the conclusion and a discussion of future work.
The diagnosis of DM has been studied using various techniques (Zarkogianni et al. 2015). One popular method involves using risk score calculators such as the American Diabetes Association calculator,9 QDiabetes,10 CANRISK,11 and Diabetes Australia.12 Regarding diabetes complications, risk engines include the global diabetes model (GDM) (Brown et al. 2000). However, such calculators are not sufficient for diabetes diagnosis, as they are based on a small number of features, and the features are collected in a crisp format for numerical features and a string format for categorical features. Shankaracharya et al. (2010) identified a list of the most critical features required to diagnose diabetes. Various modeling approaches, along with different combinations of data acquired from heterogeneous sources, can be used to provide a clinically meaningful output (Zarkogianni et al. 2015). A CDSS is required at the point of care (Zarkogianni et al. 2015). The development of such systems depends on the availability of systematic, structured, and computable knowledge bases. Zarkogianni et al. (2015) reviewed recent trends in CDSS regarding diabetes management. Although different approaches and technologies have been proposed since 1960, there remain open gaps that need to be bridged. CDSS must be integrated as a component in an EHR environment (Zhang et al. 2016). However, the full integration of CDSS in modern clinical environments has not yet been fully achieved (Sanchez et al. 2013). One of the most suitable solutions for enhancing CDSS semantics and the interoperability, integrity, and reusability of CDSS knowledge is to utilize standard ontologies (Schrim and Mitraka 2015). Standard ontologies are ontologies built using existing standard medical terminologies or ontologies such as SCT, UMLS, LOINC, GO, DOID, RxNorm, BFO, and OGMS.
Ontology-based CDSS for clinical diagnosis has been extensively investigated in many medical studies (Zhang et al. 2014). For the modeling of diseases, DOID is a general ontology, which collects the concepts associated with many diseases (Schrim and Mitraka 2015). Suzuki et al. (2015) asserted that specific ontologies must be developed for specific diseases, because every disease includes knowledge that is specific to that disease. In diabetes, ontologies have been used for every aspect of diabetes management (Chen et al. 2012; Rahimi et al. 2014). For example, Chen et al. (2012) used an ontology to build a recommendation system for drug selection. Rahimi et al. (2014) developed a type 2 diabetes mellitus (T2DM) ontology (DMO), to diagnose and manage patients with diabetes. They proposed an algorithm to query the ePBRN data repository in order to diagnose T2DM. Chalortham et al. (2009) proposed a type-II diabetes ontology. Lin and Sakamoto (2009) defined the ontology of glucose metabolism disorder (OGMD). This is applied to the ontology of geographical regions (OGR) and the ontology of genetic susceptibility factor (OGSF), which describes the genetic susceptibility factors related to diabetes mellitus. This ontology is largely related to diabetes-related complications. The BioMedBridges Diabetes Ontology (http://www.bioportal.bioontology.org/ontologies/DIAB) has been proposed based on SCT taxonomy. This ontology is mainly concerned with diabetes-related phenotypes. Although there are a growing number of ontologies for DM, there has been no attempt to establish a common framework and to collect, organize, and share formal knowledge regarding a complete picture of DM diagnosis.
Chen et al. (2012) introduced an ontology for diabetes medication, and an ontology for the symptoms of patients. These ontologies utilize the Semantic Web Rule Language (SWRL) and Java Expert System Shell (JESS) to determine potential prescriptions for patients. Sherimon et al. (2014) proposed a dynamic adaptive questionnaire ontology for gathering the medical histories of diabetic patients. Hayuhardhika et al. (2014) developed an ontology of the diabetes disease and used a weighted tree similarity algorithm for diagnosis. However, the majority of these studies have not built complete ontologies. In addition, none of these ontologies has been built using a systematic method, and they are not based on globally agreed standard top-level ontologies such as BFO. Moreover, such ontologies are not suitable for an accurate diabetes diagnosis, because none of them integrate the symptoms, laboratory tests, drugs, and diseases that affect a physician’s decision. The most critical issue is that the majority of these studies have built a demo ontology and used it as a knowledge base for implementing CDSS by using SWRL and JESS. This technique has not been adopted for many other diseases. For example, Suzuki et al. (2015) have proposed a separate ontology for periodontitis, Button et al. (2013) for the rehabilitation of knee conditions, Mugzach et al. (2015) for autism spectrum disorder, and The Infectious Disease Ontology (IDO)13 has been proposed for infectious diseases.
We have searched existing literature, including ScienceDirect, IEEE Xplore, Google Scholar, Springer Link, and PubMed for available studies regarding diabetes management ontologies and the topic of CDSS. In addition, ontology libraries have been searched, including BioPortal (BioPortal repository 2016) and the Open Biomedical Ontology (OBO) Foundry (OBO 2016). We have found that there have been many studies regarding disease-specific ontologies and ontology-based CDSS, but there has been no research regarding the building of complete DM diagnosis ontologies that contain all the necessary features and are developed in a systematic way by using widely applied standard medical and top-level ontologies. All of the existing studies are insufficient. On the other hand, when we searched for other diseases, such as Alzheimer’s, we were able to find self-contained ontologies that can be utilized in diverse CDSS applications (Malhotra et al. 2014).
With this motivation, in this paper we aim to build a comprehensive, correct, consistent, and standard OWL 2 diabetes diagnosis ontology. This global ontology follows in full the rules set by the OBO Foundry consortium (Smith et al. 2007). This ontology can serve many purposes, including decision support and interoperability with EHR. We keep in mind two pre-requisites. First, that the ontology must achieve maximum interoperability, and second that it will be amenable to future expansion that adds aspects, such as treatments, that are not included in the initial version.
DDO is an ongoing project, which aims to represent every facet of the diabetes disease accurately, in as much detail as possible. These details include, among others, their clinical presentation, diagnosis, treatment, physical manifestation, course of development, and laboratory tests. DDO is presently in the first stages of development. The fact that the ontology is perfectly created based on well-designed top-level ontologies, i.e., BFO 2 and OGMS, and existing standard ontologies, such as disease ontology and SCT, facilitates reusability and continuous enhancement. Therefore, in the future we will enrich the system with aspects of medication, including appropriate diabetic food, diet, drugs, drug–drug interactions, drug–food interactions, exercises, drug–disease interactions, education programs, and temporal aspects. Moreover, in the future, we will utilize these ontologies to build a diabetes management CDSS, based on semantic and fuzzy reasoning. Diabetes CPG can be added into the ontology in the form of rules by using SWRL, which can be queried using SQWRL or SPARQL. The uncertain nature of diabetes diagnosis can be modeled using fuzzy semantic rules, such as f-SWRL, semantically enhanced regular fuzzy systems, or fuzzy ontology. All of these future targets depend critically on the current stage of building a complete, well-designed, and standard ontology. In 2015, Hempo et al. (2015) attempted to build such an ontology, but they developed a shallow and local ontology that is not standardized.
By the word standardized, we specifically mean that the ontology obtains its concepts from standard ontologies and is built using standard upper-level ontologies. The concentration on standardization is motivated by the fact that the same knowledge can be modeled differently by using different ontology engineering methodologies. Moreover, many engineering errors are present in existing ontologies. For example, Ahmed (2011) proposed an ontology for the management of diabetes type-II, which included the facts that “a diabetes type 2 complication is_a diabetes type 2″ and “Hyperinsulinemia is_a diabetes type 2.” These axioms are not correct.
In this section, we describe the construction of DDO. It is based on standard ontologies, to ensure a shared understanding between people and an interoperability between systems (Mohammed and Benlamri 2014). No existing ontology establishes relationships between all of the terms and vocabulary relating to diabetes complications, symptoms, and medications. We can rely on existing terminologies such as SCT. However, such terminologies are huge and involve many limitations regarding ontological design (López-García et al. 2014). On the contrary, the building of ontologies based on small and precise subsets of these standard ontologies is well documented for many applications (López-García et al. 2014).
For this reason, there is a need for an effective way to create a diabetes ontology to fit the decision support purpose. To enhance interoperability, consistency, sharing, portability, and reusability, our ontology must be extracted from existing standard ontologies and terminologies (Malhotra et al. 2014). An ontology alignment technique can be employed. This entails the idea of combining multiple ontologies to create a single one, where defining the relationships between the concepts of the ontologies forms the new ontology. There are two main approaches to alignment: ontology matching and ontology linking. Ontology matching techniques are used to relate ontologies on the same domain or on partially overlapping domains (Doan et al. 2003), while ontology linking allows elements from distinct ontologies to be coupled using links (Homola and Serafini 2010). Because linked ontologies are disjoint, the ontology linking technique is appropriate for building DDO.
In addition, DDO is compliant with the principles of the OBO Foundry (OBO 2016). BFO provides the top-level concepts, which are independent of any specific domain. Using BFO as a foundation, OGMS expands the range of representational units of BFO, to include the concepts of general medical science. This consists of approximately 100 terms that describe the fundamental aspects of medicine such as ‘disorder’, ‘diagnosis’, ‘disease’, ‘disease course’, ‘symptom’, and ‘syndrome’. DDO seeks to produce definitions in a similar manner within the domain of DM.
DDO is developed following a top-down and bottom-up approach to catalog relevant entities, relationships, and attributes. We employ a top-down approach for creating high-level or generic classes in DDO by analyzing the types of diabetes complications, drugs, symptoms, laboratory tests, and so on that are presented in clinical literature and determining how to classify them within the ontology. Like GO, which contains three main sub-ontologies (biological process, cellular component, and molecular function), DDO focuses on eight main areas (i.e., disease, symptom, disorder, chemical substance, drug, demographics, physical examination, and laboratory tests). The bottom-up approach involves consulting primary research articles, review articles, the texts of CPGs, books, and medical professionals to inform the development of DDO (U.S. Department of Health and Human Services 2016; American Diabetes Association 2016; Canadian Diabetes Association 2016; National Institute for Health and Care Excellence (NICE) 2016). Domain experts provide constructive feedback and guide decision-making regarding controversial material. This approach provides and refines the majority of classes and definitions in DDO. The bottom-up approach leads to the inclusion of new terms in DDO, as well as more detailed classifications of particular concepts. Both approaches are necessary for the completion of the project.
By adhering to the OGMS and BFO frameworks, DDO is consistent and developed collaboratively with other ontologies that use OGMS. Within our diabetes domain, we reuse the most recent, prominent, and standard ontologies, including DOID (Schrim and Mitraka 2015), ontology of glucose metabolism disorder (OGMD),14 RxNorm 2015 release,15 and symptom ontology (SYMP),16 to create a hierarchical set of concepts stored in an OWL 2 ontology. The SCT 2015 release is utilized to enrich all of these ontologies, as described in (Saitwal et al. 2012). In these ontologies, terms are the core concepts and include abstract groups, sets, collections, or types of objects. The words concept, class, and term are used interchangeably. Note that individuals (or instances) are the basic ground level objects of an ontology. However, an ontology need not include any individuals to be more general (La-Ongsri and Roddick 2015). The methodology of building an ontology based on reusing existing ontologies has been employed in many studies such as for PeriO (Suzuki et al. 2015) for periodontitis, TRAK (Button et al. 2013) for rehabilitation of knee conditions, and by Mugzach et al. (2015) for an autism spectrum disorder ontology.
SCT standard terminology represents the most comprehensive medical ontology. It contains around 400,000 active concepts, including their descriptions and relationships. It is owned and distributed around the world by the International Health Terminology Standards Development Organization (IHTSDO).
DOID standard ontology began in 2003 as part of the NUgene project at the Northwestern University. It contains over 8600 known human diseases and 14,600 terms extracted from many ontologies, including SCT 2010, ICD 9, and MeSH. Presently, it has been adopted by the OBO Foundry. DOID is freely available under the Creative Commons Attribution 3.0 Unported License (http://www.creativecommons.org/licenses/by/3.0/). The SYMP standard ontology was developed in 2005 at the Institute for Genome Sciences (IGS) at the University of Maryland. Today, it contains more than 900 symptoms. RxNorm is a thesaurus, taxonomy, ontology, nomenclature, and coding system that provides normalized names and concept codes (called RxCUI) for clinical drugs. Its coverage rate is 99.995 % (Saitwal et al. 2012). This ontology was represented in the OWL 2 language as a single hierarchical structure, using the Protégé editor (http://www.protege.stanford.edu). We extract subsets of the participating ontologies for specific diabetes complications, symptoms, and medications. For example, a subset of DOID has been used to create a cancer ontology named DO_cancer_slim with only 393 cancer concepts (Wu et al. 2015). SCT concepts can extend some DOID concepts that are related to diabetes complications.
DDO engineering phases
Scope and purpose determination
In this phase, the purpose and scope of DDO are determined. DDO has only one specific purpose, which is disease diagnosis. Moreover, it has a specific scope, which is diabetes mellitus.
What are the patient’s laboratory test results?
What are the patient’s demographic data?
What are the patient’s current complications?
What are the patient’s symptoms?
What are the patient’s physical examination results?
What drugs does the patient currently take that may affect glucose level or pancreas function, and what are the chemical ingredients in these drugs?
What are the possible diagnoses for diabetic patients?
DDO must have the ability to answer these questions. Moreover, these questions will guide the next steps, including the ontology evaluation.
This step consists of five sequential steps to collect related diabetes diagnosis terms and build the full ontology. The following sections discuss these steps in more detail.
Examples of knowledge types represented in DDO ontology
A set of tests to measure the level of blood glucose, and others
Blood glucose tests: HbA1C, 2 h OGTT, FPG, RPG
Hematological profile: prothrombin INR, red cell count, Hbg, hematocrit (PCV), MCV, MCH, MCHC, platelet count, white cell count, basophils, lymphocytes, monocytes, eosinophils
Kidney function laboratory tests: serum potassium, serum urea, serum uric acid, serum creatinine, serum sodium
Lipid profile: LDL cholesterol, total cholesterol, triglycerides, HDL cholesterol
Tumor markers: FERRITIN, AFP serum, CA-125
urine analysis: chemical examination (protein, blood, bilirubin, glucose, ketones, urobilinogen)
Microscopic examination (pus, red blood cells (RBcs), crystals)
Liver function tests: serum albumin, total bilirubin, direct bilirubin, SGOT (AST), SGPT (ALT), alk phosphatase, γ GT, total protein
Females history: amenorrhea, birth, dysmenorrhea
Diseases that are often present with diabetes (diabetes complications)
Acute: cardiomyopathy, bacterial infection, ketoacidosis, obesity, ovarian disease, neoplastic disease, etc
Chronic: nonvascular such as dental disease, kidney disease, skin disease, sexual disease, and gastropathy; vascular such as macrovascular and microvascular
The set of common diabetes symptoms
Weight loss, polyuria (increased urination), polydipsia (increased thirst), and polyphagia (increased hunger), weight gain, blurred vision, etc
The drugs that increase blood glucose, and can induce diabetes either by interfering with insulin production and secretion, reducing the effectiveness of insulin in regulating metabolism, or others
Cardiovascular drugs, CNS drugs, an enzyme inhibitor, a hematologic drug, an immunotherapeutic agent, retinoid, antiallergenic drugs, and others
Reuse of ontologies
External ontologies cross-referenced in DDO
Use in DDO
Imported ontologies as whole
BFO (Basic Formal Ontology)
Top-level reference ontology
OGMS (Ontology for General Medical Science)
Mid-level reference ontology
Imported from other external ontologies
DOID (Human Disease Ontology)
Externally referenced disease classes
SYMP (Symptoms Ontology)
Select classes for symptoms
UO (Units of Measurement Ontology)
Laboratory tests units of measurements
OBO RO (Relation ontology)
Object properties design
Externally referenced drugs and chemical substances
1042 drug + 1069 substance
Imported from other external terminologies
Select classes to enhance granularity of diseases, drugs, substances, symptoms, etc.
1987 diseases, 72 symptoms, 83 laboratory tests, 1 disease course, 23 physical examinations, 5 diagnoses, 107 disorders, 23 living organisms (classes)
Selection of concepts UMLS CUIs for all concepts
The ontology is a global or abstract representation of a domain. Therefore, it does not contain instances or individuals in most cases. In our design, the ontology contains only concepts and properties. When we use the ontology to build a CDSS connected with EHR, ontology instantiation will be performed according to each set of customized patient conditions and characteristics. This customization facilitates personalized diagnosis and treatment. Moreover, the numerical values of laboratory tests have not been added, as they vary from one CPG to another.
Merging with OGMS
Specifically, a dependent continuant has two sub-concepts—BFO: realizable entity and BFO: quality. BFO: disposition is a subclass of BFO: quality, which has OGMS: disease as a subclass. This disease concept represents a certain disposition to undergo pathological processes that exist in an organism as a result of one or more disorders in that organism. A disease is a dependent continuant consisting of one or more causal chains of clinical disorders appearing in a human body and initiated by at least one disorder (Richard et al. 2009). For a detailed description of all of the BFO classes, the reader is referred to the BFO manual (Spear 2015). The OGMS: disease concept is the parent of the DDO: diabetic complication concept, which subsumes all sub-tree hierarchies representing diabetes complications. The OGMS: symptom concept is the parent of the DDO: diabetes symptom concept, which is the patient of all diabetes symptoms.
The BFO: material entity concept is the parent of the DDO: drug concept, which is the parent of all drugs affecting the level of glucose, as constructed in the drug ontology. A symptom is a bodily feature that a patient observes (2009). On the other hand, the BFO: process concept is a subclass of the BFO: occurrent concept in OGMS, and the OGMS: laboratory test concept is a subclass of the BFO: process concept. This OGMS: laboratory test concept is the parent concept of all sub-tree hierarchies representing diabetes-related laboratory tests, and OGMS: physical examination is the parent of all of a patient’s physical examinations. Finally, the OGMS: diagnosis concept in the path thing→ entity→ continuant → generally dependent continuant→ information content entity→ data item is the parent of DDO: diabetes diagnosis concept and is used to represent the concepts relating to patient diagnosis. Diagnosis is defined as “a conclusion of an interpretive process that has as input a clinical picture of a given patient and as output an assertion.” These selections of top-level concepts are performed based on the definitions of disease, diagnosis, and symptom given by Richard et al. (2009).
In this version of the ontology, only relevant OGMS concepts are used. However, other top-level OGMS terms may be added if necessary in subsequent refinements. Every OWL class has a DDO-specific CUI code, SCT concept ID, preferred name, textual definition, synonyms, and external reference ID defined using the OWL annotation properties UMLS CUI, SCT CID, preferred name, definition, synonym, and dBXrefID, respectively.
Ontology coverage check
The final step is to check the content coverage of the resulting ontology. The collected diabetes-related concepts must be represented in the optimum detailed form. There are two types of enrichment, those where a term cannot be represented in the imported ontology and those where the term can be represented in an abstract form. We refine the hierarchies by adding the absent concepts and comparing the level of granularity of existing concepts in the resulting ontology with SCT. If there are more details present in the latter, we enrich our ontology using these concepts. Concept-based mapping is used to map the remaining terms to the corresponding SCT concepts. To maximize consistency in this mapping, mapping is limited in this study to pre-coordinated concepts only (Kim et al. 2014). In other words, post-coordination is not permitted. LePendu et al. (2011) asserted that SCT concepts are suitable for DOID and symptoms enrichment. Phutthachan et al. (2014) used SCT as a source for a Thai drug ontology. SCT is required for enhancing RxNorm concepts, because RxNorm lacks a classification hierarchy (Saitwal et al. 2012). For example, to enhance the drug concept hierarchy, we use the SCT concept: 373873005|pharmaceutical/biologic product. To enhance the diabetes complication concept, we use the concept: 64572001|disease. For symptoms, we use the concept 404684003|clinical finding, and for laboratory tests we use the concept: 71388002|procedure, and in particular its sub-concept 122869004|measurements. Using some SCT browsers, such as cliniClue (http://www.cliniclue.com/cliniclue_xplore), and the UMLS metathesaurus browser (https://www.uts.nlm.nih.gov/metathesaurus.html), we collect all concepts that do not exist in the existing reused ontologies and enhance the granularity of the hierarchies of the reused concepts. We collect all of the parents and the tree of sub-concepts for each existing concept. For each non-existing concept, we use exact matching with SCT terms to determine the equivalent SCT concept. The determined concept is then added to its parents and sub-tree concepts.
Regarding the DOID ontology, DDO imports 1760 disease concepts from the 6598 DOID diseases, which constitutes 26.67 % of the total DOID concepts. DDO contains 3780 disease concepts. Disease concepts imported from DOID represent 46.56 % of the DDO disease concepts. The remaining 2020 (53.44 %) disease concepts are imported from SCT, either as new concepts that did not exist in DOID, such as retinopathy and coma, or as sub-concepts of DOID diseases, such as respiratory system disease or acute pancreatitis, where we add 17 children concepts from SCT.
Regarding the OGMD ontology, the OGMD ontology was originally designed without any standard top-level ontology. Moreover, all concepts of OGMD are directly imported from the SCT concepts disorder of glucose metabolism|126877002 and diabetic complication|74627003. As a result, we decided to ignore this ontology and work directly with SCT, because many of its concepts are represented in an abstract form than in SCT. For example, the concept hyperglycemia|80394007 in OGMS has one sub-concept, but SCT has 35 sub-concepts.
Regarding the RxNorm Ontology, all drug and chemical substance concepts are imported from RxNorm. DDO imports 1042 drug and 1069 chemical substance concepts from RxNorm. In addition, DDO imports some concepts from SCT to organize RxNorm into hierarchies.
Regarding the SYMP ontology, DDO imports 80 symptoms from the 840 SYMP concepts (9.52 %) that are related to diabetes diagnosis. DDO has 152 symptoms. It enriches the list of symptoms by 72 concepts, either by extending the imported SYMP concepts, such as hyperesthesia where we add six other concepts, including abdominal hyperesthesia, allodynia, and hyperalgesia, or by adding new symptom concepts such as cholestasis, foot symptoms, and neuroglycopenia. The concepts imported from SYMP represent 52.63 % of the total number of symptoms.
Evaluation is an emerging field, and involves several inherent problems (Brank et al. 2005). The ultimate goal of the ontology is to answer the defined competency questions in a complete and accurate way. The proposed competency questions guide the process of collecting diabetes diagnosis terms, and these terms guide the formulation of ontology concepts, properties, and axioms. Domain experts have tested the content coverage of DDO and it fully satisfies the competency questions. In a future study, we will use the ontology to build an interoperable CDSS project. In “Conclusion”, we provide an example of the capabilities of DDO for enhancing the semantic similarity between medical concepts and facilitating the interoperability between CDSS and EHR. There are no existing gold standards with which to compare DDO. However, DDO is built based on clinical terms collected mostly from standard CPG documents and concepts from standard ontologies. Moreover, concept properties are defined based on existing standard relationships from the RO ontology, and the taxonomic hierarchy of concepts is defined based on SCT. Finally, our focus will be on the following measures.
This checking describes the syntactic-level evaluation. The HermiT (version 1.3.8), Pellet, and FaCT++ reasoners are used with the Protégé 5 editor to check that DDO is consistent and free of errors. They do not reveal any discrepancies regarding this version of the ontology. Moreover, the Ontology Pitfall Scanner! (OOPS!)17 online tool can help to detect some of the most common pitfalls occurring in the development of ontologies. We run OOPS! on the DDO ontology to ensure that the ontology is free of such pitfalls.
Comparison with existing ontologies
DDO has achieved a 100 % content coverage. All existing ontologies related to the DM disease achieve only a limited coverage of the necessary concepts. All diabetes terms collected from a domain expert, CPGs, textbooks, and literature research are defined in DDO. Moreover, the usability of the ontology is high, because it uses standard labels for concepts. Each concept is annotated by a unique ID in the form of DDO_000000, a unique SCT concept ID, a unique UMLS CUID, a unique RxNorm RxCUI, a textual definition, and synonyms. DDO is 100 % annotated with SCT concept IDs. In future releases, the other IDs will be added. These IDs prevent redundancy.
All DDO concepts and synonyms are collected from standard sources, either from BioPortal ontologies, such as RxNorm, DIAB, SYMP, and DOID, or from standard terminologies such as SCT. DDO achieves a 100 % coverage of DIAB ontology concepts. That is, all DIAB concepts are present in DDO. Furthermore, DDO classifies concepts in a meaningful way. For example, all symptoms are sub-concepts of the “diabetes symptom” concept, and diabetes complications occur under the “disease” concept. On the other hand, 366 of the 375 concepts in DIAB are direct subclasses of the phenotype concept and no concept hierarchies exist, which reduces the semantic and inference capabilities of the DIAB ontology. In comparison with DOID, DDO provides domain-specific knowledge about diabetes diagnosis, but DOID is a general ontology. All concepts related to diabetes complications in DOID are collected in DDO, to preserve consistency with existing BioPortal ontologies. The 134 concepts in OGMD are organized into five main concepts regarding diabetes complications such as hyperglycemia, hyperinsulinism, and diabetes complication. However, the ontology is not built using a standard mechanism. It concentrates on one dimension of diabetes (i.e., complications) and achieves a limited coverage, even in the complications dimension.
The top-level classes table
# of subclasses
Subsumes all complications related to diabetes
Acute disease, chronic disease, nephropathy, foot disease, and cardiovascular
Subsumes all drugs affecting glucose level or pancreas function
Analgesic, antibacterial, antihistamine, autonomic, hematologic, retinoid, antiasthmatic, immunotherapeutic
DDO: laboratory test
Subsumes all of the required laboratory tests to diagnose diabetes
HbA1c, serum ketone, insulin antibodies, basophils count, C-peptide, serum creatinine, total cholesterol, direct bilirubin
DDO: physical examination
Subsumes the physical signs that support diagnosis decision
Smoking, physical activity, BMI, blood pressure, thyroid function, waist circumference, alcohol drinking
DDO: diabetes symptom
Subsumes all of the diabetes-related symptoms
Cholestasis, diarrhea, drowsiness, edema, emphysema, fatigue, foot symptom, hyperesthesia, nausea, numbness
Based on SCT, the high-level classes of DDO utilize extensive sub-classing to cover specific abstractions of entities.
Examples of OWL object properties (class-level association) in the DDO
Defines the patient’s current diseases
Defines the patient’s current symptoms
Defines the patient’s laboratory tests
Diabetes laboratory test
Defines diabetes associated physical examinations
Diabetes physical examination
Links the patient’s type of diagnosis with the diabetes disease type
Associates a drug or chemical substance with a disorder
Drug, chemical substance
Associates a diabetes disease course with a diabetes disease
Diabetes disease course
Determines the drugs taken by the patient
Defines a relationship between human and patient
Defines the chemical entities and drugs
Defines the measurement units of laboratory tests
Diabetes laboratory test
Measurement unit label
Defines patient demographics
Defines the patient diagnosis
Is the relationship between a disease and its symptoms
Specifies the body site affected by a condition
Disease or disorder
Total number of object properties
Data properties of DDO
Defines the Boolean value of the patient’s physical examinations
Determines the string value of some physical examination features and assigns a qualitative representation for the patient laboratory tests
Assigns a value for diabetes laboratory tests and some other features
Summarizes the risk level of having diabetes for a patient by using a linguistic value such as low_risk and high_risk
Summarizes the risk level of having diabetes for a patient by using a numerical value such as 85 %
Defines the patient’s symptoms
Total number of data properties
Saitwal et al. (2012) asserted that medical concepts could be mapped to SCT and UMLS concepts. Concept enrichment and the addition of annotations from SCT, UMLS, and Rxnorm can be performed automatically, semi-automatically, or manually. Automatic methods can employ the available files and database for each terminology such as RxNorm’s RXCONSO, the UMLS Metathesaurus’ MRCONSO table, and the three SCT data files. All of these datasets can be accessed from the UMLS website (https://www.nlm.nih.gov/research/umls/). However, automatic methods require reviewing by domain experts, and this action affects the ontology quality. As a result, this study adopts a manual process for ontology enrichment and annotation. The RxNav browser for RxNorm searching (https://www.rxnav.nlm.nih.gov/) is used to annotate drugs and chemical substances with RxNorm RxCUI. The CliniClue software package is used for SCT browsing (http://www.cliniclue.com/cliniclue_xplore) to collect SCT concept IDs, and the UMLS metathesaurus browser is used for UMLS searching, to obtain the UMLS CUID (https://uts.nlm.nih.gov/metathesaurus.html).
Results and discussion
DDO ontology metrics
Object property count
Data property count
Subclass axiom count
Annotation assertion axiom count
Logical axiom count
In an attempt to standardize the terminology used to refer to DM concepts and integrate this with other terminological sources, all DDO concepts are annotated with standard concept identifiers, synonyms, and definitions collected from SCT, UMLS, and RxNorm, where such information is available. As a result, DDO concepts are annotated with many types of additional information such as SCT concept IDs, UMLS UCIs, RxNorm CUIs, textual definitions, and alternative terms (synonyms). Synonym annotation is used to specify alternative names of concepts in DDO. This is applied to indicate alternative spelling variants and commonly used acronyms. For example, the term “obesity” is equivalent with “adiposity” and “adiposis.” As another example, the term “angina pectoris” is equivalent to “stenocardia” and “ischemic heart disease—angina.” At the same time, these concepts have unique identifiers. These representations support an interoperability and integration with CDSS and EHR systems. Lasierra et al. (2013) added physical concepts to represent SCT concept IDs, but this method doubles the number of concepts in the ontology through duplication. In the current version of DDO, every concept is associated with a specific SCT concept ID. However, additional definitions will be added in subsequent versions.
All diabetes-related complications are modeled under the diabetic complication concept in DDO. This hierarchy subsumes all diseases that are correlated with and go hand in hand with diabetes. This hierarchy contains 3781 diseases, organized under the two main concepts DDO: acute and DDO: chronic. We have built a large hierarchy of diabetes-related diseases. This large number of concepts is further subdivided into the additional classification of 1274 acute diseases and 2506 chronic diseases. The chronic diseases consist of those that are vascular (1822 concepts) and nonvascular (752 concepts). These diseases are organized into a tree, which facilitates the calculation of the semantic similarity between diseases. In this version of DDO, we concentrate mainly on the is-a relationship. Other relationships will be added in subsequent updates such as after, due to, associated with, and indicates. All diabetes symptoms are organized under the DDO: diabetes symptom concept. There are 152 concepts related to diabetes symptoms. There are 83 concepts for diabetes laboratory tests subsumed by the DDO: diabetes laboratory test concept. We add some data properties to model the quantitative and qualitative values of these tests. The physical examinations required for diabetes patients (23 concepts) were collected under the DDO: diabetes physical examination concept. All drugs (1042 concepts) that can affect sugar levels or pancreas function are grouped under the DDO: drug concept. Moreover, chemical substances (1069) that affect sugar levels are collected in the DDO: chemical substance concept. The method of representing drugs and substances is similar to that in Wang et al. (2013). The modeled drugs and chemicals are arranged in a hierarchy, which also enhances the calculation of semantic similarities between the conditions for the current patient and the rules modeled for existing knowledge. Moreover, this will enhance the subsequent implementation of diabetes medication, by facilitating the implementation of drug–drug, drug–disease, and drug–food interactions.
Diabetes diagnosis consists of four main types: diagnosis of diabetes mellitus type-I, diagnosis of diabetes mellitus type-II, diagnosis of gestational diabetes, and diagnosis of pre-diabetes. These concepts are connected to diabetes mellitus as a disease under the DDO: diabetes mellitus concept, which has 104 sub-concepts. Moreover, data properties are modeled to define the risk level associated with a diabetes diagnosis (i.e., DDO:has_risk_level and DDO_ has_risk_percent). DDO imports 17 relations from the OBO RO ontology. RO provides consistent and unambiguous formal definitions of the relations employed in biomedical ontologies (Smith et al. 2005). An individual patient is defined in terms of most of the previously modeled concepts as:
Patient ≡ role ⋀ (has_level_of_education exactly 1 ‘level of education’) ⋀ (has_demographic some demographic) ⋀ (has_lab_test some ‘diabetes laboratory test’) ⋀ (has_quality some ‘diabetes symptom’) ⋀ (has_disposition some disease) ⋀ (takes_drug some drug) ⋀ (has_diagnosis exactly 1 disease) ⋀ (has_physical_examination some ‘physical examination’) ⋀ (has_risk_level exactly 1 string) ⋀ (has_risk_percent exactly 1 float)
In addition, different EHR systems may use different coding systems. As a result, a global encoding terminology must be used to unify the clinical meaning of applied concepts. SNOMED CT is the most acceptable terminology for coding EHR data. We have previously proposed an encoding methodology for medical data by using SCT (Shaker and Elmogy 2015). Diabetes mellitus is a chronic disease, and its diagnosis requires personalization according to each individual patient’s conditions. At the same time, there are many features involved in making a diagnosis decision, which is a strain on a physician’s time. As a result, the integration between CDSS systems and EHR facilitates the collection of patient features from distributed EHRs. The physician must enter the patient’s current state only. The additional necessary features are collected from the patient’s EHR. DDO supports the semantic collection of such data. For example, the concept of renal disease can be represented differently in different hospitals, i.e., renal disease, nephropathy, and nephrosis (see Fig. 6). These concepts may be coded with different terminologies. SCT supports the mapping to many different terminologies such as ICD (Unified Medical Language System (UMLS) 2016) and LOINC (Bodenreider 2008). Moreover, SCT supports the mapping to archetypes (García et al. 2012) and HL7 RIM (Rico-Diez and 2013). In addition, concepts in ADDO are furnished with annotations noting the unique UMLS identifiers (UMLS_CUI) and RxNorm identifiers (RxCUI) of the concepts. In this way, a unified representation can be obtained. For example, see kidney disease|90708001 in Fig. 6. A unified concept (such as kidney disease|90708001) can be found directly in the ontology, or a semantic similarity algorithm can be used to find the most similar concept in DDO (Harispe et al. 2014). A physician’s knowledge implemented in the form of rules can be coded into DDO by using SWRL rules.19 For example, consider the following rule:
(FPG > 7.0 mmol/L and/or 6.0 < HbA1c < 6.4 % and OGTT > 11.0 mmol/L and age > 45 and disease = “kidney disease ” and drug = “ Phenylephrine ” and symptom = symp)→ “Type 2 diabetes”.
This is formulated by the American Diabetes Association 2015 (American Diabetes Association 2016), and can be represented in SWRL format as follows:
Patient (x), HbA1c (l1), FPG (l2), OGTT (l3), age (ag), has_lab_test (x, l1), has_lab_test (x, l2), has_lab_test (x, l3), has_quantitative_value (l1, v1), has_quantitative_value (l2, v2), has_quantitative_value (l3, v3), has_UoM (l1, “percent”), has_UoM (l2, “mmol/l”), has_UoM (l3, “mmol/l”), has_disposition (x, d), has_quantitative_Value (ag, av), Kidney_disease (d), takes_drug (x, dr), Phenylephrine (dr), has_quality (x, symp), symptom (symp), swrlb:graterthan (v2, 7.0), swrlb:graterthan (v1, 6.0), swrlb:lessthan (v1, 6.4), swrlb:graterthan (av, 45), swrlb:graterthan (v3, 11.0) -> has_diagnosis (x, diag), type_2_diabetes_mellitus (diag).
To make a decision regarding a patient, the patient is first instantiated in the ontology (i.e., the ontology ABOX). In this example, the patient data states that patient has a kidney disease, so an exact match is found between the patient feature and the rule. Expert and CPG knowledge are often represented by aggregated concepts such as cardiovascular disease or kidney disease. However, in most cases, when instantiating the ontology concepts from EHR, a patient can be described by other more specific concepts. For example, regarding kidney disease, patients can have nephritis, glomerulonephritis, or acute tubular necrosis diseases. DDO is able to discover these relationships. For example, it contains 157 concepts for kidney disease only. Semantic similarity between the collected patient features and DDO concepts can determine the level of similarity or applicability of a diagnosis rule. We have proposed a semantic similarity measure to calculate the clinical distances between medical concepts (Shaker et al. 2015). DDO supports the calculation of semantic similarity for diseases, drugs, chemical substances, and symptoms. As a result, the resulting decision is semantically intelligent, and any DDO-based CDSS will mimic the thinking of an expert physician. Moreover, the physician is not required to enter all of the patient’s features, because DDO ontology supports interoperability with EHR systems, and this facilitates the collection of a patient’s history. For example, in Fig. 6, the patient’s features “history of IFG,” “obesity,” and “father with type-II diabetes mellitus” are collected from the distributed EHR systems.
Limitations of the current study
The version of DDO described in this paper has some limitations. First, the ontology concentrates on the diagnosis of diabetes, and no treatments have been discussed. Further studies will add treatment aspects, including medications, foods, education, diet, physical exercise programs, drug–drug interactions, and drug-and-disease interactions. In addition, this study has only focused on the creation of the ontology. Future research could implement a complete CDSS system connected with the EHR environment. The system could use a rule-based reasoning mechanism implemented using SWRL rules supported by the ontology, and use inference engines such as JESS or Pellet. Moreover, the ontology concepts have only been annotated with SCT concept IDs. Future studies could annotate the concepts with UMLS CUIDs, RxNorm RxCUI, synonyms, and textual definitions. Many axioms can be added to the ontology to model the relationships between drugs and ingredients, diseases, diseases and drugs, and diseases and disorders. As a result, future studies will enhance the logic of the ontology with such axioms. Finally, this study only focused on best practices regarding otology development and domain knowledge content. Thus, our future work will also include the design of evaluation studies to assess how successfully DDO supports CDSS of diabetes diagnosis.
The purpose of this study was to develop a theoretically sound and semantically intelligent knowledge base for solving problems related to the diagnosis of diabetes. Such knowledge can enable a new class of patient-centric CDSS that can help physicians to diagnose diabetics quickly and accurately. DDO provides a standard ontology that can support the interoperability between CDSS and healthcare systems. Moreover, it can be used in combination with a rule base to build a rule-based diabetes diagnosis system. The ontology is comprehensive, as it contains all diabetes-related complications, laboratory tests, symptoms, physical exams, demographics, and diagnoses. DDO is the first reported diabetes disease ontology developed to represent different disease aspects in a formal logical format. Future work will concentrate on using DDO to build a CDSS system. Moreover, the ontology annotations for UMLS and RxNorm ids will be completed, and the ontology will be upgraded to cover diabetes treatment, by including concepts and axioms related to diabetes medication and follow-up actions.
SES studied in depth the top-level ontologies including BFO 2.0 and OGMS, and determined the semantic locations of diabetes diagnosis concepts under these ontologies. FA studied, compared, and summarized the most recent diabetes clinical practice guidelines and diabetes diagnosis studies and modeled the needed DDO ontology parts including concepts, object and data properties, and semantic axioms. SES and FA participated in the conducted interviews with domain experts to collect the diabetes diagnosis knowledge and validated it using the recent clinical practice guidelines. To build a standard ontology, Ali collected the existing standard ontologies, including SNOMED CT and RxNorm, and modeled a mapping between the DDO terms and standard ontologies' concepts. As an ontology engineer, SES with the assistance of protégé implemented the OWL 2 ontology for DDO based on our proposed methodology. FA tested and evaluated the resulting ontology. Both authors participated equally in the preparation of the manuscript. Both authors read and approved the final manuscript.
This project was supported by King Saud University, Deanship of Scientific Research, College of Sciences, Research Centre.
The authors would like to thank Dr. Farid Badria, Prof. of Pharmacognosy, Department and head of Liver Research Lab, Mansoura University, Egypt and Dr. Hosam Zaghloul, Prof. at Clinical Pathology Department, Faculty of Medicine, Mansoura University, Egypt, for their efforts in this work.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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