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Potter, J.

Publications and source records attributed to Potter, J..

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Building a National HIV Cohort from Routine Laboratory Data: Probabilistic Record-Linkage with Graphs

BackgroundChronic disease management requires the ability to link patient records across multiple interactions with the health sector. South Africas National Health Laboratory Service (NHLS) conducts all routine laboratory monitoring for the countrys national public sector HIV program. However, the absence of a validated patient identifier has limited the potential of the NHLS database for epidemiological research, policy evaluation, and longitudinal patient care. We developed and validated a record linkage algorithm, creating a unique patient identifier and enabling analysis of the NHLS database as a national HIV cohort. To our knowledge, this is the first national HIV cohort in any low-or middle-income country.\n\nMethods.We linked data on all CD4 counts, HIV viral loads (VL), and ART workup laboratory tests from 2004-2016. Each NHLS laboratory test result is associated with a name, sex, date of birth (DOB), gender, and facility. However, due to typographical and other errors and patient mobility between facilities, different patient specimens may be associated with different sets of identifying information. We developed a graph-based probabilistic record linkage algorithm and used it to construct a unique identifier for all patients with laboratory results in the national HIV program. We used standard probabilistic linkage methods with Jaro-Winkler string comparisons and weights informed by response frequency. We also used graph concepts to guide the linkage in determining whether a cluster of patient specimens could plausibly reflect a single patient. This approach allows matching thresholds to vary with the density of the network and limits over-matching.\n\nTo train and validate our approach, we constructed a quasi-gold standard based on manual review of 59,000 candidate matches associated with 1000 randomly sampled specimens. These data were divided into training and validation sets. Domain weights and graph parameters were optimized using the manually matched training data.\n\nTo evaluate performance, we calculated the probability that a true match was correctly identified by our algorithm (sensitivity, Sen) and the probability that a match identified by our algorithm was truly a match (positive predictive value, PPV) in the manually-matched data. We also assessed validity in the full cohort using proxies for under-and over-matching and assessed sensitivity vis-a-vis national identification numbers and patient folder numbers, which were available for a sub-set of records. We compared the performance of our algorithm for exact matching and a prior identifier that had been developed by the NHLS Corporate Data Warehouse.\n\nResults.As of December 2016, the NHLS database contained 117 million patient specimens with a CD4, VL, or other laboratory test used in HIV care. These specimens had 63 million unique combinations of patient identifying information. From these data, our matching algorithm identified 11.6 million unique HIV patients who had at least one CD4 count or VL result. These patients 70.9 million total specimens, with a median of 3 specimens per patient (IQR 1 to 8). Sensitivity and PPV of the algorithm were estimated to be 93.7% and 98.6% in manually-matched data, compared to 64.1% and 100.0% for the existing NHLS identifier. We estimated that in 2016 there were 3.35 million patients on ART and virologically monitored, similar to the National Department of Health estimate of 3.50 million.\n\nConclusion.We constructed a South African National HIV Cohort by applying novel graph-based probabilistic record linkage techniques to routinely collected laboratory data, with high sensitivity and positive predictive value. Information on graph structure can guide record linkage in large populations when identifying data are limited.

epidemiology

Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history

BackgroundA number of single nucleotide polymorphisms (SNPs), which are common inherited genetic variants, have been identified that are associated with risk of colorectal cancer. The aim of this study was to determine the ability of these SNPs to estimate colorectal cancer (CRC) risk for persons with and without a family history of CRC, and the screening implications.\n\nMethodsWe estimated the association with CRC of a 45 SNP-based risk using 1,181 cases and 999 controls, and its correlation (r) with CRC risk predicted from detailed family history. We estimated the predicted change in the distribution across predefined risk categories, and implications for recommended age to commence screening, from adding SNP-based risk to family history.\n\nResultsThe inter-quintile risk ratio for colorectal cancer risk of the SNP-based risk was 2.46 (95% CI 1.91 - 3.11). SNP-based and family history-based risks were not correlated (r = 0.02). For persons with no first-degree relatives with CRC, recommended screening would commence 2 years earlier for women (4 years for men) in the highest quintile of SNP-based risk, and 12 years later for women (7 years for men) in the lowest quintile. For persons with two first-degree relatives with CRC, recommended screening would commence 15 years earlier for men and women in the highest quintile, and 8 years earlier for men and women in the lowest quintile.\n\nConclusionsRisk reclassification by 45 SNPs could inform targeted screening for CRC prevention, particularly in clinical genetics settings when mutations in high-risk genes cannot be identified.

epidemiology