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Co‐occurring defect analysis: A platform for analyzing birth defect co‐occurrence in registries
Author(s) -
Benjamin Renata H.,
Yu Xiao,
Navarro Sanchez Maria Luisa,
Chen Han,
Mitchell Laura E.,
Langlois Peter H.,
Canfield Mark A.,
Swartz Michael D.,
Scheuerle Angela E.,
Scott Daryl A.,
Northrup Hope,
Schaaf Christian P.,
Ray Joseph W.,
McLean Scott D.,
Lupo Philip J.,
Agopian A. J.
Publication year - 2019
Publication title -
birth defects research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.845
H-Index - 17
ISSN - 2472-1727
DOI - 10.1002/bdr2.1549
Subject(s) - coda , trisomy , spina bifida , pairwise comparison , computer science , medicine , pediatrics , artificial intelligence , seismology , geology , biology , genetics
Background Few studies have systematically evaluated birth defect co‐occurrence patterns, perhaps, in part, due to the lack of software designed to implement large‐scale, complex analytic methods. Methods We created an R‐based platform, “co‐occurring defect analysis” (CODA), designed to implement analyses of birth defect co‐occurrence patterns in birth defect registries. CODA uses an established algorithm for calculating the observed‐to‐expected ratio of a given birth defect combination, accounting for the known tendency of birth defects to co‐occur nonspecifically. To demonstrate CODA's feasibility, we evaluated the computational time needed to assess 2‐ to 5‐way combinations of major birth defects in the Texas Birth Defects Registry (TBDR) (1999–2014). We report on two examples of pairwise patterns, defects co‐occurring with trisomy 21 or with non‐syndromic spina bifida, to demonstrate proof‐of‐concept. Results We evaluated combinations of 175 major birth defects among 206,784 infants in the TBDR. CODA performed efficiently in the data set, analyzing 1.5 million 5‐way combinations in 18 hr. As anticipated, we identified large observed‐to‐expected ratios for the birth defects that co‐occur with trisomy 21 or spina bifida. Conclusions CODA is available for application to birth defect data sets and can be used to better understand co‐occurrence patterns. Co‐occurrence patterns elucidated by using CODA may be helpful for identifying new birth defect associations and may provide etiological insights regarding potentially shared pathogenic mechanisms. CODA may also have wider applications, such as assessing patterns of additional types of co‐occurrence patterns in other large data sets (e.g., medical records).