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Method comparison and estimation of causal effects of insomnia on health outcomes in a survey sampled population.

TitleMethod comparison and estimation of causal effects of insomnia on health outcomes in a survey sampled population.
Publication TypePublication
Year2023
AuthorsShahu A, Chung J, Tarraf W, Ramos AR, González HM, Redline S, Cai J, Sofer T
JournalSci Rep
Volume13
Issue1
Pagination9831
Date Published2023 Jun 17
ISSN2045-2322
KeywordsCausality, Computer Simulation, Hispanic or Latino, Humans, Outcome Assessment, Health Care, Sleep Initiation and Maintenance Disorders
Abstract

Applying causal inference methods, such as weighting and matching methods, to a survey sampled population requires properly incorporating the survey weights and design to obtain effect estimates that are representative of the target population and correct standard errors (SEs). With a simulation study, we compared various approaches for incorporating the survey weights and design into weighting and matching-based causal inference methods. When the models were correctly specified, most approaches performed well. However, when a variable was treated as an unmeasured confounder and the survey weights were constructed to depend on this variable, only the matching methods that used the survey weights in causal estimation and as a covariate in matching continued to perform well. If unmeasured confounders are potentially associated with the survey sample design, we recommend that investigators include the survey weights as a covariate in matching, in addition to incorporating them in causal effect estimation. Finally, we applied the various approaches to the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) and found that insomnia has a causal association with both mild cognitive impairment (MCI) and incident hypertension 6-7 years later in the US Hispanic/Latino population.

DOI10.1038/s41598-023-36927-2
Alternate JournalSci Rep
PubMed ID37330559
PubMed Central IDPMC10276808
Grant ListP30 AG059299 / AG / NIA NIH HHS / United States
N01HC65236 / HL / NHLBI NIH HHS / United States
R01 HL161012 / HL / NHLBI NIH HHS / United States
R35 HL135818 / HL / NHLBI NIH HHS / United States
N01HC65233 / HL / NHLBI NIH HHS / United States
R21 AG056952 / AG / NIA NIH HHS / United States
R01 AG048642 / AG / NIA NIH HHS / United States
RF1 AG061022 / AG / NIA NIH HHS / United States
N01HC65235 / HL / NHLBI NIH HHS / United States
P30 AG062429 / AG / NIA NIH HHS / United States
RF1 AG054548 / AG / NIA NIH HHS / United States
N01HC65234 / HL / NHLBI NIH HHS / United States
N01HC65237 / HL / NHLBI NIH HHS / United States
R21 AG070644 / AG / NIA NIH HHS / United States
HHSN268201000001I / HL / NHLBI NIH HHS / United States
MS#: 
1185
Manuscript Lead/Corresponding Author Affiliation: 
HCHS/SOL Genetic Analysis Center - University of Washington, Seattle
ECI: 
Yes
Manuscript Status: 
Published