Phenotyping Down syndrome: discovery and predictive modelling with electronic medical records

被引:0
|
作者
Nguyen, T. Q. [1 ,2 ]
Kerley, C. I. [3 ]
Key, A. P. [1 ,4 ,5 ]
Maxwell-Horn, A. C. [6 ]
Wells, Q. S. [7 ]
Neul, J. L. [1 ,4 ,6 ]
Cutting, L. E. [1 ,2 ,4 ,6 ]
Landman, B. A. [1 ,3 ,4 ]
机构
[1] Vanderbilt Univ, Vanderbilt Brain Inst, Nashville, TN 37240 USA
[2] Vanderbilt Univ, Peabody Coll Educ & Human Dev, Nashville, TN USA
[3] Vanderbilt Univ, Sch Engn, Nashville, TN 37240 USA
[4] Vanderbilt Univ, Vanderbilt Kennedy Ctr, Med Ctr, Nashville, TN 37240 USA
[5] Vanderbilt Univ, Med Ctr, Dept Speech & Hearing Sci, Nashville, TN 37240 USA
[6] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37240 USA
[7] Vanderbilt Univ, Med Ctr, Div Cardiovasc Med, Nashville, TN 37240 USA
关键词
behavioural phenotypes; Down syndrome; intellectual difference; methodology in research; HEALTH-CARE ACCESS; ATRIOVENTRICULAR SEPTAL-DEFECT; ETHNIC DISPARITIES; CHILDREN; INDIVIDUALS; HYPERTENSION; PREVALENCE; OUTCOMES; PROFILE; PEOPLE;
D O I
10.1111/jir.13124
中图分类号
G76 [特殊教育];
学科分类号
040109 ;
摘要
BackgroundIndividuals with Down syndrome (DS) have a heightened risk for various co-occurring health conditions, including congenital heart disease (CHD). In this two-part study, electronic medical records (EMRs) were leveraged to examine co-occurring health conditions among individuals with DS (Study 1) and to investigate health conditions linked to surgical intervention among DS cases with CHD (Study 2).MethodsDe-identified EMRs were acquired from Vanderbilt University Medical Center and facilitated creating a cohort of N = 2282 DS cases (55% females), along with comparison groups for each study. In Study 1, DS cases were one-by-two sex and age matched with samples of case-controls and of individuals with other intellectual and developmental difficulties (IDDs). The phenome-disease association study (PheDAS) strategy was employed to reveal co-occurring health conditions in DS versus comparison groups, which were then ranked for how often they are discussed in relation to DS using the PubMed database and Novelty Finding Index. In Study 2, a subset of DS individuals with CHD [N = 1098 (48%)] were identified to create longitudinal data for N = 204 cases with surgical intervention (19%) versus 204 case-controls. Data were included in predictive models and assessed which model-based health conditions, when more prevalent, would increase the likelihood of surgical intervention.ResultsIn Study 1, relative to case-controls and those with other IDDs, co-occurring health conditions among individuals with DS were confirmed to include heart failure, pulmonary heart disease, atrioventricular block, heart transplant/surgery and primary pulmonary hypertension (circulatory); hypothyroidism (endocrine/metabolic); and speech and language disorder and Alzheimer's disease (neurological/mental). Findings also revealed more versus less prevalent co-occurring health conditions in individuals with DS when comparing with those with other IDDs. Findings with high Novelty Finding Index were abnormal electrocardiogram, non-rheumatic aortic valve disorders and heart failure (circulatory); acid-base balance disorder (endocrine/metabolism); and abnormal blood chemistry (symptoms). In Study 2, the predictive models revealed that among individuals with DS and CHD, presence of health conditions such as congestive heart failure (circulatory), valvular heart disease and cardiac shunt (congenital), and pleural effusion and pulmonary collapse (respiratory) were associated with increased likelihood of surgical intervention.ConclusionsResearch efforts using EMRs and rigorous statistical methods could shed light on the complexity in health profile among individuals with DS and other IDDs and motivate precision-care development.
引用
收藏
页码:491 / 511
页数:21
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