Joint Modeling of Individual Trajectories, Within-Individual Variability, and a Later Outcome: Systolic Blood Pressure Through Childhood and Left Ventricular Mass in Early Adulthood. Issue 4 (15th October 2020)

• Record Type: Journal Article
• Authors: Parker, Richard M A; Leckie, George; Goldstein, Harvey; Howe, Laura D; Heron, Jon; Hughes, Alun D; Phillippo, David M; Tilling, Kate
• Is Part Of: American journal of epidemiology. Volume 190:Issue 4(2021)
• Page Start: 652
• Page End: 662
• Publication Date: 2020-10-15
• Subjects: ALSPAC -- Bayesian analysis -- blood pressure -- children -- joint model -- left ventricular hypertrophy -- longitudinal studies -- young adult; Epidemiology -- Periodicals; Public health -- Periodicals; 614.4
• DOI: 10.1093/aje/kwaa224
• Languages: English
• ISSNs: 0002-9262

Abstract

Abstract: Within-individual variability of repeatedly measured exposures might predict later outcomes (e.g., blood pressure (BP) variability (BPV) is an independent cardiovascular risk factor above and beyond mean BP). Because 2-stage methods, known to introduce bias, are typically used to investigate such associations, we introduce a joint modeling approach, examining associations of mean BP and BPV across childhood with left ventricular mass (indexed to height; LVMI) in early adulthood with data (collected 1990–2011) from the UK Avon Longitudinal Study of Parents and Children cohort. Using multilevel models, we allowed BPV to vary between individuals (a "random effect") as well as to depend on covariates (allowing for heteroskedasticity). We further distinguished within-clinic variability ("measurement error") from visit-to-visit BPV. BPV was predicted to be greater at older ages, at higher body weights, and in female participants and was positively correlated with mean BP. BPV had a weak positive association with LVMI (10% increase in within-individual BP variance was predicted to increase LVMI by 0.21%, 95% credible interval: −0.23, 0.69), but this association became negative (−0.78%, 95% credible interval: −2.54, 0.22) once the effect of mean BP on LVMI was adjusted for. This joint modeling approach offers a flexible method of relating repeatedly measured exposures to later outcomes.