Journal of Healthcare Engineering
Volume 2017 (2017), Article ID 3818302, 10 pages
https://doi.org/10.1155/2017/3818302

Research Article

Semantic Modeling for Exposomics with Exploratory Evaluation in Clinical Context

Jung-wei Fan,1,2,3 Jianrong Li,1,2,3 and Yves A. Lussier1,2,3,4

¹Department of Medicine, The University of Arizona, Tucson, AZ, USA
²BIO5 Institute, The University of Arizona, Tucson, AZ, USA
³Center for Biomedical Informatics & Biostatistics, The University of Arizona, Tucson, AZ, USA
⁴Cancer Center, The University of Arizona, Tucson, AZ, USA

Correspondence should be addressed to Jung-wei Fan; fanj@email.arizona.edu and Yves A. Lussier; yves@email.arizona.edu

Received 24 April 2017; Revised 26 June 2017; Accepted 30 July 2017; Published 30 August 2017

Academic Editor: Cui Tao

Copyright © 2017 Jung-wei Fan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Exposome is a critical dimension in the precision medicine paradigm. Effective representation of exposomics knowledge is instrumental to melding nongenetic factors into data analytics for clinical research. There is still limited work in (1) modeling exposome entities and relations with proper integration to mainstream ontologies and (2) systematically studying their presence in clinical context. Through selected ontological relations, we developed a template-driven approach to identifying exposome concepts from the Unified Medical Language System (UMLS). The derived concepts were evaluated in terms of literature coverage and the ability to assist in annotating clinical text. The generated semantic model represents rich domain knowledge about exposure events (454 pairs of relations between exposure and outcome). Additionally, a list of 5667 disorder concepts with microbial etiology was created for inferred pathogen exposures. The model consistently covered about 90% of PubMed literature on exposure-induced iatrogenic diseases over 10 years (2001–2010). The model contributed to the efficiency of exposome annotation in clinical text by filtering out 78% of irrelevant machine annotations. Analysis into 50 annotated discharge summaries helped advance our understanding of the exposome information in clinical text. This pilot study demonstrated feasibility of semiautomatically developing a useful semantic resource for exposomics.

1. Introduction

Precision medicine represents a paradigm of conducting biomedical research and practice by considering individual variation—genes, environment, and lifestyle [1]. Environmental and lifestyle factors play a critical role in our health and are known to interact with the genetic components through an epigenetic process [2]. The concept of exposome [3], which first came about in 2005, stands for all nongenetic factors that a person is exposed to throughout a lifetime. Common examples are pollutants, tobacco/alcohol use, occupational hazards, and even psychosocial stress such as being a victim of abuse. Exposome science has received increasing attention in precision medicine and has evolved into an interdisciplinary field across biology, genomics, public health, statistics, and informatics [4]. In order to capture the full picture of various health-related contexts, it is essential to incorporate exposome parameters into knowledge engineering and data analytics [5].

Whenever exposome is mentioned, common understanding refers to environmental conditions and self-induced exposures in social history. In fact, there has been a growing interest in using social history information (e.g., substance use and occupation) from clinical text [6–8]. On the other hand, often overlooked are exposures in clinical settings, many of which are the consequence of healthcare activities. Given the simplified equation “phenotype = genotype × environment,” extensive research has focused on phenotyping [9] from electronic health records (EHRs). Likewise, we propose that it is equally important to investigate all exposome information available in EHRs, a task dubbed as “expotyping” [10]. Dr. Vertosick Jr’s quote, “You ain’t never the same when the air hits your brain” [11] easily explains the implication that any procedure, especially a major one like craniotomy (plus the complication of anesthetics), may have a lingering effect on one’s health (e.g., postoperative cognitive dysfunction [12]). In addition, research has revealed that even life-saving procedures could paradoxically result in an adverse outcome (e.g., ventilator-induced lung injury), depending on the subtle interplay with a patient’s genetic predisposition [13]. Fortunately, modern EHRs can actually serve as a primary data source for tracing all types of clinical exposome on a patient. Another notable category is pathogen exposures, which often occur in disguise as diseases that can be deterministically attributed to a specific microbe. However, the challenge remains on how we can model and extract such abundant exposome information from EHRs.

Despite the diverse exposome data available in EHRs, there is still a dearth of systematic work on modeling and extraction. Possible explanations are (1) many healthcare activities are not perceived as exposures, (2) most research concentrate only on a narrow set of study-specific exposures, or (3) there is a lack of semantic resources available for assisting in the identification of exposome information in the EHRs. The most pertinent modeling framework we found was the Exposure Ontology (ExO) [14], which maps out key exposome concepts such as exposure event, stressor, and the relations among them. However, ExO is a bare skeleton that has not been filled with cross-references to concepts in other major terminologies and currently has limited coverage over the diverse clinical exposome of interest. To bridge these gaps with a focus on systematically investigating exposures in clinical contexts, we aimed to semiautomatically derive a semantic framework as well as explored its usability in facilitating exposome annotation of narrative EHRs. Our semantic modeling consisted of a subset of the Unified Medical Language System (UMLS) and, therefore, was interoperable with major biomedical terminologies. The interest in narrative EHRs was based on empirical knowledge that the texts not only serve as a good source of environmental/lifestyle factors but also document extensive clinical exposures (e.g., procedures). The annotation was meant to obtain general assessments on what exposome information is described in the clinical text, which would then lay the foundation for developing extraction tools and for discovering disease associations down the road.

The objectives of this study were (1) to create an exposome-oriented semantic network from existing ontology entities and relations, (2) to perform exploratory evaluation on the semantic adequacy and usability in clinical contexts, and (3) to summarize the properties of exposome concepts found in EHRs. In summary, our exposome subnetwork represented rich domain knowledge, including 454 pairs of exposure and outcome semantic types. The subnetwork concepts consistently covered about 90% of PubMed literature on exposure-induced iatrogenic diseases over a 10-year period. The subnetwork filtered out 78% of irrelevant machine outputs in the exposome annotation of 50 discharge summaries. Analysis of the annotations offers insights into the exposome presence in clinical contexts and feedback for existing ontology resources.

2. Materials and Methods

2.1. The UMLS and Semantic Network

The UMLS [15] is the world’s largest integrated biomedical terminology framework maintained by the U.S. National Library of Medicine (NLM). The UMLS has three major components: the Metathesaurus (META), the Semantic Network (SN), and the Specialist LEXICON. The META unifies concepts from multiple source terminologies and ontologies into individual Concept Unique Identifiers (CUIs). As of the end of 2016, it contained more than three million concepts from 199 sources. The META includes files that host rich semantic information. The MRCONSO.RRF is the main file that collects comprehensive synonymous entities of the sources under each CUI. The MRSTY.RRF file links each CUI to their corresponding SN semantic type(s). The MRREL.RRF file preserves fine-grained semantic relations from source ontologies such as SNOMED-CT [16]. The SN currently contains 127 semantic types (e.g., T037 Injury or Poisoning) and 54 distinct semantic relations. The SN relations can be traced back to their origin from the NLM’s Medical Subject Headings (MeSH) and are categorized as either hierarchical (is-a) or nonhierarchical (e.g., type A causes type B) [17]. For use cases that do not require fine granularity, there is also a mapping that aggregates the SN types into coarser semantic groups [18].

2.2. The i2b2 NLP Challenge Corpus

For studying the distribution and properties of exposome concepts in clinical texts, we used de-identified notes from the i2b2 NLP (Natural Language Processing) Research Data Sets that consist of medical records from institutions such as Partners HealthCare. With roughly a decade of history, the i2b2 challenges [19] facilitated clinical NLP research that varied from fundamental (e.g., coreference resolution) to end applications (e.g., identifying obesity). The 2006 corpus [20] for tasks of de-identification and smoking status classification was chosen for the current study—specifically a subset of Partners 889 raw discharge summaries without any annotation. The 2006 subset was chosen because the section headers occurred mostly with explicit uppercase patterns, making automated detection easier for computing section-wise distribution of the concept annotations. Further, the corpus had sentence boundaries predetected and therefore reduced the NLP effort. In a generalizability evaluation, we also used 73 independent discharge summaries from Beth Israel Deaconess Medical Center (or simply “Beth” hereafter), which was part of the i2b2 2010 corpus.

2.3. Extract Exposure-Related Semantic Types

To identify exposure-related semantic types, we started with disorder-related semantic types. This strategy was based on the assumption that any exposure event would generally result in a certain negative health effect. Figure 1(a) illustrates our inference process using an event-driven template that has been framed into the question: What nongenetic factors could contribute to a disorder? The template was used to search the SRSTRE2 file of SN, which contained fully inherited relations among the semantic types. The disorder semantic types were obtained via the Disorder (DISO) of the SN semantic groups [18]. All the DISO semantic types were included except for T050 Experimental Model of Disease, which indicates an artificial setting. We manually determined four semantic relations that would involve a DISO type in an exposure (abbreviated as EXPO) event:

(1)DISO is result_of EXPO.(2)DISO is associated_with EXPO.(3)EXPO causes DISO.(4)EXPO complicates DISO.

(a) Identifying exposure semantic types via relations with disorders

(b) Identifying disease concepts in relation with microbe exposures

Figure 1: Ontology-assisted selection of exposome concepts.

Many of the candidate EXPO semantic types matched the template; however, not all of them also fit into the context of an exposure event. For example, T019 Congenital Abnormality associated_with T040 Organism Function does not fit, as the latter is not a qualified EXPO type. Manual curation was performed over all candidate EXPO types suggested by the template, and only those that really meant an EXPO→DISO event were kept.

2.4. Extract Disease Concepts of Microbial Etiology

To identify microbe exposure where only the disease is mentioned, we used fine-grained semantic relations in the META MRREL.RRF file. The file contains semantic relations among UMLS concepts that were populated from the source ontologies. We reviewed all relations in MRREL.RRF and chose the causative_agent_of from SNOMED-CT to form a template. Figure 1(b) illustrates our inference process of using the template. We manually determined three specific semantic types that represent the most common microbial exposures: T004 Fungus, T005 Virus, and T007 Bacterium. Searching with the template is equivalent to asking “the microbe concept is a causative_agent_of what?” The outcome slot is simply filled by selecting any concept that belongs to the DISO semantic group as described in the previous section. As a result, each identified disorder actually stands for “ever being exposed to” a responsible microbe, based on the domain knowledge modeled in SNOMED-CT.

2.5. Evaluate the Semantic Adequacy for Covering Clinical Exposome Literature

To evaluate if the semantic modeling reasonably covered domain knowledge on clinical exposome, we used PubMed literature about exposure-induced iatrogenic diseases during 2001–2010. The range to 2010 was used because PubMed records of the most recent years might be still being indexed and not reflect a stabilized view for the bibliometric purpose. The benchmark set consisted of 1248 PubMed IDs (PMIDs) from the query: “adverse effects”[sh] AND iatrogenic[ti] AND (“2001/01/01”[PDAT]: “2010/12/31”[PDAT]). The MeSH terms of the PMIDs were automatically extracted and mapped to CUIs using the MRCONSO.RRF source and synonym information. Given the CUIs of the MeSH terms, we were able to compute which MeSH terms belonged to the exposure or disease semantic types of our derived exposome subnetwork. Note that for a MeSH to qualify as an exposure, we also required it to be followed by the subheading “adverse effects” or any of its children “toxicity” and “poisoning.” For a PMID to be counted as being covered by the subnetwork, at least one MeSH had to belong to an exposure semantic type (plus proper subheading) and at least one MeSH belonging to a disease semantic type as in one of the covered EXPO-DISO relations (refer to Supplement available online at https://doi.org/10.1155/2017/3818302). The chronological trends were summarized for the number of covered PMIDs and exposure-disease pairs, as well as the percentage of covered PMIDs and the average number of exposure-disease pairs per PMID.

2.6. Perform Exposome Annotation and Analysis in Clinical Text

For batch preannotation, the MetaMap [21] program (2016 version) was used to identify UMLS concepts in the 889 Partners discharge summaries. From the MetaMap-identified concepts, we filtered by keeping only those either with an exposure semantic type or of a microbe-caused disorder. In addition, regular expression (uppercase phrase followed by colon) was used to mark the section headers for calculation of section-wise distribution of the concepts. To obtain a more reliable summary of the exposome annotations, the first author (Ph.D. in biomedical informatics) manually curated the machine-identified candidate concepts in 50 random discharge summaries that had an explicit social history section. In terms of size, this subcorpus had an average of 115 sentences (or 1124 tokens) per document, and the average sentence length was 9.5 tokens. The curation involved verifying exposures that were present to the patient and correcting any mislabeled sections. The process was facilitated by using the brat annotation tool [22]. Based on the curated annotations, we calculated descriptive statistics of the concept distribution over different sections and semantic types. As a rough assessment of reproducibility, we used the curated exposure annotations to (case-insensitively) exact-match into 73 independent Beth discharge summaries and compared the distribution of sections that contained those exposures. Lastly, qualitative analysis was performed to understand characteristics of the exposome concepts and limitations of the existing ontology resources.

3. Results and Discussion

3.1. Modeling of Exposome Semantic Types and Concepts

The methods of Figure 1(a) obtained 454 EXPO-DISO pairs that were linked via the relations causes, complicates, associated_with, and results_of. There were 41 distinct exposure semantic types involved in these relations. The full list of the curated semantic type pairs is available in Supplement . The EXPO-DISO pairs represent a comprehensive network of semantic types involved in exposure events. To provide a peek into the model contents, Figure 2 visualizes a partial network showing only exposure semantic types that are directly related to T020 Acquired Abnormality. Pointing outward are the relations result_of and associated_with, for example, Acquired Abnormality as result_of Therapeutic or Preventive Procedure. Inversely, the exposure nodes point to the center with the relations causes and complicates, for example, Pharmacologic Substance causes Acquired Abnormality. We color-coded the exposure nodes according to their broader UMLS semantic groups. It can be seen that Chemicals & Drugs (in green) dominate about half of the types, followed by Procedures (in purple), and then Activities & Behaviors (in indigo). The methods described in Figure 1(b) identified 5667 microbe-induced disorder concepts. Examples are shown in Table 1, and the full list is available in Supplement 2.

Figure 2: A partial network of exposome semantic types and their relations to health outcome. The colors of the exposure nodes stand for different broad semantic groups that the semantic types belong to.

Table 1: Example disease concepts of microbial etiology.

Disease CUI
Disease name
Disease semantic type
Microbe CUI
Microbe name
Microbe semantic type

C0006057
Botulism
T037 Injury or Poisoning
C0009055
Clostridium botulinum
T007 Bacterium

C0275677
Miscarriage due to Leptospira
T046 Pathologic Function
T0023358
Leptospira
T007 Bacterium

C0376618
Endotoxemia
T033 Finding
C0018150
Gram-negative bacteria
T007 Bacterium

C0266024
Moon’s molar teeth
T019 Congenital Abnormality
C0040840
Treponema pallidum
T007 Bacterium

C0032768
Postherpetic neuralgia
T047 Disease or Syndrome
C0042338
Human herpesvirus 3
T005 Virus

C0032371
Poliomyelitis
T047 Disease or Syndrome
C0206435
Human poliovirus
T005 Virus

C1535939
Pneumocystis jiroveci pneumonia
T047 Disease or Syndrome
C0320385
Pneumocystis jiroveci
T004 Fungus

C0029307
Oroya Fever
T047 Disease or Syndrome
C0318324
Bartonella bacilliformis
T007 Bacterium

Concepts that did occur in the study corpus.

The results demonstrate rich domain knowledge that can be extracted from existing ontology. The derived subnetwork models comprehensive interactions involved in exposure events. One advantage of using the UMLS is that it allows linking the semantic framework to individual biomedical concepts and their source terminologies for versatile integration. The application of our methods offers great potential for enriching existing resources such as the ExO, which provides a core skeleton but lacks the integration with concepts of major terminologies. Our deliverable of the microbial disorder concepts can serve as a useful resource itself, especially for use cases dealing with infectious diseases. In the list, we also observed an interesting disorder, C0014522 Epidermodysplasia verruciformis, which is an autosomal recessive inherited skin disease that features wart-like lesion due to infection with the human papillomavirus (HPV). It echoes the importance of investigating subtle interplay between our genome and exposome in order to fully understand certain health conditions. In terms of methodology, our semantic filtering based on relational template demonstrates a useful ontological approach for selecting task-specific entities of interest.

3.2. Semantic Adequacy of the Derived Exposome Subnetwork

For assessing whether our semantic framework adequately accommodates evolving evidence-based medicine, Figure 3 shows the trends of covered literature on exposure-induced iatrogenic diseases—which represent the primary area of interest in clinical exposome. In Figure 3(a), the red line indicates a steady increase of PMIDs that had at least one exposure-disease MeSH pair covered by our subnetwork. In terms of the distinct exposure-disease pairs, the blue line indicates corresponding growth over the 10 years. Table 2 provides actual examples of the covered MeSH pairs and their host PMIDs. More importantly, not only do the counts indicate the coverage scales with the knowledge growth but the orange line in Figure 3(b) indicates that the percentage of PMIDs with covered exposure-disease pairs remained consistently high (mean = 90.59%, standard deviation = 0.02%). The green line shows that the average number of covered exposure-disease pairs per PMID climbed mildly over the years. As for the peak in the green line, it is unclear why in 2004 there was a sudden surge of research findings. Despite marginal errors in the bibliometrics-oriented evaluation, we believe it reasonably corroborates the reliability and scalability of our semantic modeling. In addition, since our subnetwork is derived from the UMLS, any update in the SN (though infrequent) can be incorporated on a regular basis.

(a) Number of exposure-disease MeSH pairs and number of PMIDs that had at least one such pair covered by the derived exposome subnetwork

(b) Percentage of PMIDs that had at least one covered exposure-disease MeSH pair and the average number of such MeSH pairs per PMID

Figure 3: Semantic coverage of exposure-induced iatrogenic diseases in PubMed from 2001 to 2010.

Table 2: Example exposure-disease MeSH pairs (and their semantic types) covered by our exposome subnetwork.

PMID
Exposure MeSH
Exposure semantic type
Disease MeSH
Disease semantic type

20736205
Anti-Arrhythmia Agents
T121 Pharmacologic Substance
Hallucinations
T048 Mental or Behavioral Dysfunction

11337626
Osteotomy
T061 Therapeutic or Preventive Procedure
Kyphosis
T190 Anatomical Abnormality

11387778
Colonoscopy
T060 Diagnostic Procedure
Intestinal Perforation
T047 Disease or Syndrome

11581058
Prostheses and Implants
T074 Medical Device
Lacrimal Duct Obstruction
T190 Anatomical Abnormality

11747288
HIV Protease Inhibitors
T121 Pharmacologic Substance
Lipodystrophy
T047 Disease or Syndrome

11984961
Dental Restoration, Permanent
T122 Biomedical or Dental Material
Systemic Inflammatory Response Syndrome
T047 Disease or Syndrome

12043843
Haloperidol
T109 Organic Chemical
T121 Pharmacologic Substance
Basal Ganglia Diseases
T047 Disease or Syndrome

12106934
Cardiac Catheterization
T058 Health Care Activity
Arteriovenous Fistula
T190 Anatomical Abnormality

3.3. Exposome Annotations in the Clinical Text

The filter of exposome semantic types and concepts consistently reduced the number of entities required for manual review. Specifically for the 50 random discharge summaries, an average of 77.72% presumably irrelevant (i.e., nonexposome) MetaMap annotations was filtered out. After the manual curation, the median number of annotations per note was 36 (min: 9, max: 118). According to the data use agreement, we will contribute our annotations back to the i2b2 clinical NLP repository. By aggregating counts across the notes, the top 20 sections with the curated exposome annotations are shown in Table 3. Due to the inpatient context of discharge summaries, the top section turned out to be HOSPITAL COURSE, which essentially covers all procedures and medications administered during a patient’s hospitalization. Aligning with expectation, SOCIAL HISTORY ranked moderately high (the 8th) in the list. There were six medication-related sections in the top 20, which reflected drugs being a preeminent exposure in a clinical setting. The sections HISTORY OF PRESENT ILLNESS (the 2nd) and PAST MEDICAL HISTORY (the 7th) also hosted a decent amount of exposome annotations. As the assessment of generalizability across independent institution/dataset, Table 4 shows that we not only found many of the identical exposure terms in the Beth corpus (the column “# annotations” was based on exact-string search) but the sections hosting those terms also exhibit high similarity in terms of name and rank (comparing to Table 3). For example, the top two sections, HOSPITAL COURSE and HISTORY OF PRESENT ILLNESS, are identical. In Table 5, we list the top 20 semantic types of the curated concepts. The top two types, T121 Pharmacologic Substance and T109 Organic Chemical, are from drugs, consistent with the high prevalence of medication-related sections as in Table 3. The second cluster consists of T061 Therapeutic or Preventive Procedure and T060 Diagnostic Procedure, with most of them mentioned in HOSPITAL COURSE (not shown in the table). The type T055 Individual Behavior (e.g., use of alcohol or tobacco) mostly resides in SOCIAL HISTORY. For further inspection, Supplement 3 includes the details of the annotation counts ranked in two levels: first by section and then by semantic type.

Table 3: Top 20 sections with exposure annotations in the 50 Partners discharge summaries.

Rank
Section name
# annotations

1
HOSPITAL COURSE
617

2
HISTORY OF PRESENT ILLNESS
418

3
DISCHARGE MEDICATIONS
344

4
MEDICATIONS ON ADMISSION
321

5
MEDICATIONS ON DISCHARGE
309

6
MEDICATIONS
178

7
PAST MEDICAL HISTORY
89

8
SOCIAL HISTORY
87

9
ALLERGIES
47

10
MEDICATIONS ON TRANSFER
45

11
HOSPITAL COURSE BY SYSTEM
40

12
ADMISSION MEDICATIONS
40

13
RELEVANT LABORATORY DATA
38

14
LABORATORY DATA
36

15
HOSPITAL COURSE AND TREATMENT
35

16
HOSPITALIZATION COURSE
29

17
PHYSICAL EXAMINATION
22

18
PAST SURGICAL HISTORY
22

19
IDENTIFYING DATA
19

20
DISCHARGE INSTRUCTIONS
18

Table 4: Top 20 sections with exposure annotations in the 73 Beth discharge summaries.

Rank
Section name
# annotations

1
HOSPITAL COURSE
492

2
HISTORY OF PRESENT ILLNESS
386

3
BRIEF HOSPITAL COURSE
353

4
DISCHARGE MEDICATIONS
267

5
MEDICATIONS ON ADMISSION
157

6
PERTINENT RESULTS
148

7
DISCHARGE INSTRUCTIONS
114

8
DISP
103

9
SOCIAL HISTORY
93

10
PAST MEDICAL HISTORY
92

11
SIGNED ELECTRONICALLY BY
69

12
INDICATION
45

13
THE FOLLOWING ISSUES WERE ADDRESSED DURING THIS HOSPITAL ADMISSION
44

14
GASTROINTESTINAL
44

15
SERVICE
43

16
IMPRESSION
41

17
COURSE IN HOSPITAL
40

18
ALLERGIES
40

19
LABORATORY DATA
38

20
MAJOR SURGICAL OR INVASIVE PROCEDURE
35

Table 5: Top 20 semantic types of the exposure annotations in the 50 Partners discharge summaries.

Rank
Semantic type
# annotations

1
T121: Pharmacologic Substance
927

2
T109: Organic Chemical
874

3
T061: Therapeutic or Preventive Procedure
281

4
T060: Diagnostic Procedure
278

5
T195: Antibiotic
105

6
T116: Amino Acid, Peptide, or Protein
72

7
T074: Medical Device
64

8
T033: Finding
47

9
T197: Inorganic Chemical
38

10
T125: Hormone
36

11
T047: Disease or Syndrome
30

12
T200: Clinical Drug
29

13
T127: Vitamin
27

14
T055: Individual Behavior
24

15
T007: Bacterium
15

16
T097: Professional or Occupational Group
14

17
T129: Immunologic Factor
14

18
T114: Nucleic Acid, Nucleoside, or Nucleotide
13

19
T058: Health Care Activity
12

20
T037: Injury or Poisoning
12

The results show that our exposome semantic modeling helped prefilter about 78% of irrelevant concepts before the manual curation. Our attention to microbe-based exposures was justified: Although minor in proportion, the two types, T047 Disease or Syndrome (those of microbial etiology) and T007 Bacterium, made it into the second half of Table 5 (the 11th and 15th, resp.). Medications were found to form the majority of the clinical exposome, which echoes a previous work that also presented drugs as an “environmental” factor in EHRs [23]. Given the exposures predominantly being medications and procedures, one could argue that using structured EHR data would save the redundant effort of extracting them from text. However, it requires further investigation to understand how much data would be missed if using only structured data. For example, a previous study showed that provider notes are complementary to structured data for recording of medication intensification [24] and that we should take into account any over-the-counter products documented in history narratives. It is noteworthy that HISTORY OF PRESENT ILLNESS and PAST MEDICAL HISTORY ranked among the top 10 sections in Table 3, suggesting that the history sections that are generally included in most clinical notes (not just discharge summary) can host abundant exposome information. Among the exposome-containing sections, SOCIAL HISTORY should be considered as different by nature, for it distinctly covers most of the “nonclinical” exposomes encountered in a patient’s daily life. In one specific note, the social history even documented exposure to a nuclear accident in the patient’s past residence.

A pertinent question that emerged in the study was “to what extent could we generalize the definition of exposome?” We annotated concepts such as retirement and widowhood (both T033 Finding) as exposures, given that studies have shown their association with health [25, 26]. However, would it make sense to also treat any significant biological event such as pregnancy as an exposure? This remains an open subject of future research. Interestingly, an infrequent category of exposures revealed one blind spot of our semantic modeling, which could partially be attributed to limitations in the UMLS semantic classification. We came across several exposure concepts such as C3496069 Cocaine Use and C0206073 Domestic Violence, which were classified to type T048 Mental or Behavioral Dysfunction. However, the filter criteria missed them because we did not consider T048 to be a causal role (the exposure slot) in our event template, and none of these health issues had microbial etiology. It definitely takes more consideration for reclassifying and modeling these abusive behaviors (affecting self or others) as exposures.

3.4. Limitations

Although we believe the high-level trends to be reliable, the PubMed-based coverage evaluation might involve some marginal errors inevitably. Only discharge summary was utilized in this study, which does not represent all types of clinical text. As an exploratory evaluation, the exposome annotations were curated by only one annotator (JF) and therefore not free from bias. With the aim of just assessing what exposome concepts exist, we did not engage in annotating any advanced attributes such as intensity (dosage), duration, and frequency. Relatedly, we did not attempt to optimize the NLP methods for extracting exposome concepts; instead, we concentrated on understanding the high-level distribution and characteristics of the final annotations.

3.5. Future Work

We will consider seeking collaboration with the ExO development team to unify the solutions and make it a sustainable resource for the exposome science community. Beyond serving the coverage evaluation, we will build a knowledge base of clinical exposome by refining our PubMed query and postprocessing pipeline. For rigorous annotation, multiple annotators will be used and with agreement metrics computed. The annotation criteria are to be expanded by including pertinent attributes (e.g., exposure intensity) and documented in a formal guideline. The annotations can be used to train NLP systems for cohort identification in clinical exposome studies. Ultimately, a more thorough expotyping approach should be pursued to integrate both structured and unstructured EHR data.

4. Conclusions

We developed a semiautomated approach for modeling exposome semantics and assessing the usability in clinical contexts. The modeling leveraged event templates to identify exposure concepts that had ontological relations with disease outcomes. A subnetwork was derived from the UMLS, representing 454 pairs of relations between exposure and outcome semantic types. The subnetwork was able to cover 90% of PubMed literature on exposure-induced iatrogenic diseases from 2001 to 2010. For identifying exposome concepts in 50 discharge summaries, the subnetwork improved the efficiency by filtering out 78% of irrelevant machine annotations. The exposome concepts exhibited diverse presence of semantic types and sections in the annotated corpus. Analysis into the results expanded our understanding of the clinical narratives and ontology resources. This work demonstrated the value of semantics-powered methods for advancing exposome science and precision medicine.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.

Acknowledgments

This work was supported in part by The University of Arizona Health Sciences CB2, the BIO5 Institute, and NIH (U01AI122275, HL132532, CA023074, 1UG3OD023171, 1R01AG053589-01A1, and 1S10RR029030). The authors thank Dr. Colleen Kenost for the help with the English editing. De-identified clinical records used in this research were provided by the i2b2 National Center for Biomedical Computing funded by U54LM008748 and were originally prepared for the Shared Tasks for Challenges in NLP for Clinical Data organized by Dr. Ozlem Uzuner, i2b2 and SUNY.

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