Volume 13 Supplement 13
Graph-based signal integration for high-throughput phenotyping
© Herskovic et al; licensee BioMed Central Ltd. 2012
Published: 24 August 2012
Electronic Health Records aggregated in Clinical Data Warehouses (CDWs) promise to revolutionize Comparative Effectiveness Research and suggest new avenues of research. However, the effectiveness of CDWs is diminished by the lack of properly labeled data. We present a novel approach that integrates knowledge from the CDW, the biomedical literature, and the Unified Medical Language System (UMLS) to perform high-throughput phenotyping. In this paper, we automatically construct a graphical knowledge model and then use it to phenotype breast cancer patients. We compare the performance of this approach to using MetaMap when labeling records.
MetaMap's overall accuracy at identifying breast cancer patients was 51.1% (n=428); recall=85.4%, precision=26.2%, and F1=40.1%. Our unsupervised graph-based high-throughput phenotyping had accuracy of 84.1%; recall=46.3%, precision=61.2%, and F1=52.8%.
We conclude that our approach is a promising alternative for unsupervised high-throughput phenotyping.
Electronic Health Records (EHR) collect patient data obtained in the course of clinical care. These records, when aggregated in Clinical Data Warehouses (CDWs), are a rich source of data for research. For example, we may want to estimate disease prevalence, track infectious diseases, identify unexpected side-effects of drugs, identify cohorts of patients for studies and compare the effectiveness of alternative treatments for a given condition.
Unfortunately, CDWs built from EHRs have not lived up to these hopes. The fundamental problem is that we are attempting to use EHR data for purposes other than supporting clinical care. Over 20 years ago, van der Lei warned against this practice and proposed that “Data shall be used only for the purpose for which they were collected.”  For example, ICD-9-CM codes are routinely assigned to a patient for billing purposes, but billing rules are not meant to preserve and encode clinical reality. Instead, billing rules are meant to comply with the byzantine, sometimes mutually incompatible requirements of insurers, administrators, and regulators. For example, patients and their insurers are billed only for conditions for which they are treated by providers. In multiple-provider situations this means that each provider only sees a part of the patients’ conditions.
For example, consider a patient P with breast cancer that gets her oncological treatment at Cancer Center A. Cancer Center A bills the patient, and the patient’s insurance, for cancer care. The same patient gets tonsillitis and decides to go to outpatient clinic B. Clinic B sees her, treats her, and bills her insurance for tonsillitis. At this point in time, Cancer Center A has a record for a patient with breast cancer, and Clinic B has a record for a patient with tonsillitis.
This state of affairs is appropriate for routine clincal care. Somewhere in the patient’s record at Clinic B a physician or nurse will have written that the patient also had breast cancer. If another physician at Clinic B needs to know, she can find out by reading the patient’s file.
Now consider a researcher at Clinic B who wants to know if breast cancer predisposes people towards tonsillitis. Any attempt to find a correlation using billing data will miss patient P. The same is true for researchers trying to perform genomics research on these diseases; they will simply miss these patients.
This is not idle speculation; at our outpatient clinic, approximately 52% of patients who have or had breast cancer according to their own charts have been billed for the condition. Similarly, 23% of patients with endometrial cancer have a billing code compatible with endometrial cancer . Data from other institutions and other conditions are similar. For example, 52% of patients with an ICD-9-CM code for Wegener’s Granulomatosis at St. Alexius Medical Center actually met the diagnostic criteria for the condition . A strategy combining different ICD-9 codes yielded an 88% positive predictive value (PPV) for Lupus Nephritis cases at Brigham & Women’s Hospital in Boston. However, the sensitivity was impossible to compute (i.e., it was not known how many cases were missed) . Other studies had similar outcomes [5–10].
Many research efforts such as those focused on Comparative Effectiveness Research (CER), genomics, proteomics, genealogy require accurate knowledge of the patient’s entire medical history and list of conditions; sometime referred to as the patient’s phenotype. These research endeavors aren’t interested in the patient’s billing history. They are interested in what conditions the patients actually had. This is also known as high-throughput phenotyping.
This information is often available in physicians’ and nurses’ notes. Further, clinical notes will contain information about past events, unlike other sources of information. For example, a patient with a remote past history of breast cancer, now without evidence of disease, will not receive medications, and will not have procedures or lab exams done that could point to the diagnosis. Clinical notes may also be more abundant than other sources of information. Our CDW contains 295,000 patients with at least one clinical note; 161,000 patients with at least one recorded vital sign; 143,000 patients with at least one medication in a structured field; and 138,000 patients with at least one lab exam. Thus, clinical notes are an important resource for research projects that require clinical information.
Manual review of hundreds of thousands of charts is impractical. Even smaller-scale manual review is expensive, and prone to error and inconsistent coding . The biomedial informatics reserch community therefore continuously seeks ways to extract computable information from free text . Automated coding systems such as MetaMap , cTAKES , and MedLEE  can map text to Unified Medical Language System (UMLS) concepts; however, without the addition of customized rules they draw no inferences from it. Many interesting problems require determining the state of the patient – i.e. “did the patient ever have breast cancer?” instead of the easier “does this document mention breast cancer?” Automated classification systems built using Weka or MAVERIC’s ARC  address the second need, and perform very well on cross-validation [2, 17]. However, these systems have two weaknesses. The first weakness is that they require training data, which are expensive and slow to create, as it requires a clinician to read each patient’s chart and decide whether the patient had the condition in question. The second weakness is that a system that works well to identify one concept may not work as well to identify a different concept, or even the same concept in another data set; in other words, these systems are not generalizable .
We therefore set out to build a high-throughput phenotyping system that required neither training data nor customized disease-specific rules, used available external knowledge, and performed well compared to existing automated coding systems. We based our design on the intuition that clinicians first look for explicit statements that assert that a patient has the condition of interest. If they fail to find these statements, they look for evidence of the condition. For example, the question “does the patient have diabetes?” can be answered by finding a statement in the notes that asserts that the patient has diabetes. However, if the explicit assertion is missing, it is still possible to determine whether the patient has diabetes by looking for concepts that are commonly associated with diabetes. Thus, a physician might read the chart and discover that the patient had high glycosylated hemoglobin (a lab marker of long-term glucose concentration in blood), takes metformin (a drug used to treat diabetes), and had a foot exam (commonly performed on patients with diabetes during office visits). The presence or absence these additional elements may add evidence for or against a diagnosis of diabetes respectively, in the event that the concept is explicitly mentioned. In other words, human experts use background knowledge to understand text; specifically, they look for consistency between multiple concepts found in the text.In many respects, this process mirrors the construction and integration phases of Kintsch’s influential construction-integration model of text comprehension: concepts derived from both the reader’s background knowledge and elements of the text itself are integrated during the process of constructing a mental representation of the text, and the extent to which these concepts are collectively consistent with a particular interpretation (e.g., patient has diabetes) determines whether or not this interpretation prevails.
We imitate this comprehension process  by constructing a nearest neighbor graph using a limited breadth-first search from a seed term on UMLS concepts extracted from our CDW, to simulate associative retrieval of related concepts during the process of text comprehension. We also simulate the imposition of external knowledge not explicitly mentioned in the record by using knowledge from the UMLS and the biomedical literature to curate the graph. Finally, we use spreading activation on the graph to simulate the integration component of Kintsch’s model, which resolves inconsistencies by spreading activation across the links between concepts, such that concepts that are contextually consistent will ultimately be more activated.
Sources of data
We used four different data sources: 1. UMLS concepts extracted from the clinical notes in our CDW using MetaMap ; 2. A Reflective Random Indexing (RRI) representation of the UMLS concepts [19, 20]; 3. The relationships in the 2010 AA UMLS Metathesaurus; 4. A database of semantic predications extracted from the biomedical literature using SemRep . The relationships derived from the metathesaurus and SemRep were used to select conceptual relations that were more likely to be clinically relevant, as RRI alone draws a measure of general relatedness between concepts only.
Our experiment consisted of four phases: 1. Compute a measure of pairwise correlation between UMLS concepts extracted from the entire CDW; 2. Build a nearest neighbor graph of UMLS concepts based on this pairwise correlation measure; 3. Use the graph to perform inference on a patient-by-patient basis.
Computing a measure of pairwise correlation between UMLS concepts
We used MetaMap (http://metamap.nlm.nih.gov)  to extract UMLS concepts from 1,540,173 clinical notes belonging to outpatient records for 260,772 patients in the UTHealth CDW, after excluding patients in the test dataset (described below). We generated a file for each individual patient containing the UMLS Concept Unique Identifier (CUI) for each UMLS concept identified by MetaMap within that patient’s record, thereby creating a representation of each patient as a "bag of concepts". However, given the large dimensionality of the UMLS (over 2,500,000 unique concepts), a naïve representation of each unique concept as a dimension would be very sparse.
We therefore used Reflective Random Indexing (RRI) , a variant of Random Indexing  to derive a measure of the similarity between pairs of concepts, as implemented in the Semantic Vectors software package (http://code.google.com/p/semanticvectors/) [22, 23]. The random indexing paradigm involves the generation of a semantic vector representation of a given concept by superposition of randomly constructed elemental vector s representing the contexts in which the concept occurs [22, 23]. First, we generated random elemental vectors, 1000-dimensional sparse vectors that are mutually orthogonal or close-to-orthogonal, for each CUI. Then, we generated a semantic vector for each document in the corpus of clinical notes by adding the elemental vector for every CUI extracted by MetaMap from a given document using log-entropy weighting to emphasize CUIs that occur focally in the corpus, and normalized the result. Finally, we built a second set of vectors for each UMLS concept (i.e. CUI) by adding the document vectors for every document in which a given CUI occurs, and normalizing this result by dividing every dimension by the length of the vector.This second set was called the semantic concept vectors.
The semantic vector representation allowed us to compute the relatedness between any pair of CUIs in our CDW by calculating the cosine of the angle between their semantic vector representations. In other words, we computed the Vector Cosine Comparison (VCC) between pairs of vectors. The pairs with the highest VCC were most closely correlated. The advantage of using a semantic vector representation is that their small dimensionality allows a very large number of vectors in RAM simultaneously. The ability to keep the entire vector store in RAM makes the computations extremely fast.
Constructing a nearest-neighbors graph
We built a nearest-neighbors graph by starting with a seed concept (in this case, C0006142, Malignant neoplasm of breast), then performing a breadth-first search adding the nearest neighborss to the seed (i.e., the concepts with the semantic vectors that had the highest VCC to the seed concept). We recursively iterated through the most closely-related concepts to the seed concept, and added any previously unseen concepts to the graph. We added up to six concepts at each level, and recursed at most three times to limit the size of the graph. In other words, the first level added six concepts; the second level, up to 36 concepts (six for each concept in the first level); the third level, up to 216 (63). If a concept was already present in the graph, it was not added again. We selected the thresholds arbitrarily, based on the observation that human beings have a working memory of between five and nine items . We used the result of the VCC between concepts in the CDW as the weight of the edge.
Nearest-neighbor graphs tend to be noisy as RRI does not capture the nature of the relationship between concepts; we therefore used computable knowledge from the literature and the UMLS to filter the graph. We checked each nearest-neighbor relation against two databases. We removed relations that were absent in both databases from the graph. One database was the UMLS Metathesaurus. Any relationship between two concepts present in the Metathesaurus was enough to validate the nearest-neighbor relationship. The second database was a set of triples (concept-relationship-concept) extracted from the literature by SemRep from a set of 10,000,000 biomedical articles in PubMed. If the relationship was present in either database, it was kept, and labeled with the name of the relationship (either from the UMLS or the literature).
Perform inference on a patient-by-patient basis
We instantiated and manipulated the graphs with our own MEDRank software (https://github.com/drh-uth/MEDRank, ). After instantiating the graph for each patient, every concept was assigned a starting value of 0. We populated each patient’s graph with concepts extracted by MetaMap from that patient’s clinical notes. MetaMap produces a confidence score between 0 and 1000 for each instance of a concept in a given document. We mapped these scores linearly to the range [0,1]. We then added all normalized confidence scores for each concept for each patient. We considered UMLS concepts that were not found in the patient’s record to have a score of 0. For every concept in the graph, we set its starting activation to the sum of its normalized confidence scores in all of a patient’s notes.
After populating the graph for a single patient, we spread activation along the graph's edges for a maximum of three steps. The new activation for each node was the sum of its weighted incoming weights, minus the weight it spread to other nodes. We then read the value of the node corresponding to the original seed concept, and used this as the output of the process.
We created a test set by taking a random sample of 10,000 records of our CDW. We then eliminated records that did not meet our inclusion criteria (Additional file 1). The remaining 428 records were reviewed by a clinician (PBS), who labeled them as "Breast Cancer" (meaning that the patient had, at some point in his or her life, been diagnosed with any kind breast cancer) or "No breast cancer" meaning that the patient had never been diagnosed with breast cancer.
Our baseline was the performance of MetaMap acting as an automated coding system. We compared this to the performance of our graph-based spreading activation system.
The outcome measure was the ability to discover the state of the patient as determined by the clinician. We counted the number of true positives, true negatives, false positives, and false negatives for the computed state of the patient. We calculated the precision, recall, F1 (harmonic mean of precision and recall), and overall accuracy of the automated process.
By measuring the peformance of MetaMap using this outcome measure with and without the graph-based process, we were able to determine how the graph-based process changed the quality of concept extraction.
Our test set contained 428 patients. Of these 428 patients, 82 had breast cancer (19.2%) and 346 (80.8%) did not.
Performance of MetaMap and the graphical method on determining the breast cancer status of the patient as determined by a physician
Our graph-based process complements MetaMap by leveraging structured knowledge (the UMLS) and predicate triples obtained from the literature. It requires no training or manual adjustments, improves overall accuracy and F1. We were able to use graph-based techniques to successfully integrate signals from our clinical records, the UMLS, and the biomedical literature.
To better understand MetaMap’s performance, we examined 10 false positives. In all 10 cases, breast cancer was mentioned in relation to the patient's family history. Unfortunately, developing a reasonable rule-based system to eliminate family-history related false positives is difficult. There are many different ways in which the relationship is described, from "Patient has a sister who may have had breast cancer" to "Family history: Breast cancer -- grandmother." Although we considered removing text labeled “family history” from the clinical notes, the text may be part of a longer narrative section, or may have one of several different, sometimes ambiguous headers. Developing a system to reliably detect family history references is analogous to detecting breast cancer references in the first place. In other words, it is a subtle text classification problem that may require intensive development and fine-tuning at each insititution.
On the other hand, we acknowledge that we are showing merely a proof of concept. While we believe that our technique has great potential, we are presenting only a single condition for which it works.
We have not yet leveraged the different kinds of relationships between concepts in the graph to improve performance. It is possible that TREATS and DIAGNOSES relationships, for example, are much more important than IS_A or parent/child relationships from the UMLS for the purposes of discovering patients with a certain condition.
Our graph construction process was inspired by a high-level understanding of clinician reasoning (i.e. "Does the file say that the patient has breast cancer? If not, does it say that the patient has been treated with procedures commonly used to treat breast cancer?"), but it does not reflect a formal model of diagnosis. The parameters we used in this study were inspired by cognitive models of text comprehension, in which elements of the text and associations from the mind of the reader are integrated, and discrepancies resolved through spreading activation such that the ultimate representation favors those concepts that are contextually appropriate (i.e., mutually consistent).
Additionally, although the completely unsupervised graph-based discovery approach presented here worked well, it may work even better with some human input. For example, Tamoxifen is almost exclusively used to treat breast cancer, and it was not discovered by the graph-building process. We believe that it was not discovered in this study because its strength of association in our CDW is low, due to the fact that our breast oncological practice is small and focused on surgical treatment. It is likely to appear in graphs built at other institutions, and adding it manually to the graph would potentially improve its generalizability.
Although we demonstrate our technique on breast cancer, the methodology will clearly apply to other diseases. In the near future we will undertake the necessary test data set construction to evaluate how well the graph-based technique generalizes to other conditions.
Graph-based approaches can leverage existing external knowledge to improve concept extraction from clinical text. Unlike previous approaches to this problem, it requires neither the development of customized rules, nor the construction of an expert-annotated training set for supervised machine learning. It outperforms MetaMap when identifying breast cancer patients. Since this approach is disease-independent, it has the potential to generalize to other conditions.
This work was supported in part by NCRR Grant 3UL1RR024148 and NCRR Grant 1RC1RR028254.
This article has been published as part of BMC Bioinformatics Volume 13 Supplement 13, 2012: Selected articles from The 8th Annual Biotechnology and Bioinformatics Symposium (BIOT-2011). The full contents of the supplement are available online at http://www.biomedcentral.com/1471-2105/13/S13/S1
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