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Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions.
Xu, Hanfei; Schwander, Karen; Brown, Michael R; Wang, Wenyi; Waken, R J; Boerwinkle, Eric; Cupples, L Adrienne; de Las Fuentes, Lisa; van Heemst, Diana; Osazuwa-Peters, Oyomoare; de Vries, Paul S; van Dijk, Ko Willems; Sung, Yun Ju; Zhang, Xiaoyu; Morrison, Alanna C; Rao, D C; Noordam, Raymond; Liu, Ching-Ti.
Afiliación
  • Xu H; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA. hfxu@bu.edu.
  • Schwander K; Division of Statistical Genomics, Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Brown MR; Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, the University of Texas School of Public health, Houston, TX, USA.
  • Wang W; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Waken RJ; Field and Environmental Data Science, Benson Hill Inc, St. Louis, MO, USA.
  • Boerwinkle E; Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, the University of Texas School of Public health, Houston, TX, USA.
  • Cupples LA; The Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
  • de Las Fuentes L; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • van Heemst D; NHLBI and Boston University Framingham Heart Study, Framingham, MA, USA.
  • Osazuwa-Peters O; Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.
  • de Vries PS; Section of Gerontology and Geriatrics, Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
  • van Dijk KW; Department of Population Health Sciences, Duke University, Durham, NC, USA.
  • Sung YJ; Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, the University of Texas School of Public health, Houston, TX, USA.
  • Zhang X; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Morrison AC; Division of Endocrinology, Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
  • Rao DC; Leiden Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, the Netherlands.
  • Noordam R; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
  • Liu CT; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Eur J Hum Genet ; 29(5): 839-850, 2021 05.
Article en En | MEDLINE | ID: mdl-33500576
ABSTRACT
Recent studies consider lifestyle risk score (LRS), an aggregation of multiple lifestyle exposures, in identifying association of gene-lifestyle interaction with disease traits. However, not all cohorts have data on all lifestyle factors, leading to increased heterogeneity in the environmental exposure in collaborative meta-analyses. We compared and evaluated four approaches (Naïve, Safe, Complete and Moderator Approaches) to handle the missingness in LRS-stratified meta-analyses under various scenarios. Compared to "benchmark" results with all lifestyle factors available for all cohorts, the Complete Approach, which included only cohorts with all lifestyle components, was underpowered due to lower sample size, and the Naïve Approach, which utilized all available data and ignored the missingness, was slightly inflated. The Safe Approach, which used all data in LRS-exposed group and only included cohorts with all lifestyle factors available in the LRS-unexposed group, and the Moderator Approach, which handled missingness via moderator meta-regression, were both slightly conservative and yielded almost identical p values. We also evaluated the performance of the Safe Approach under different scenarios. We observed that the larger the proportion of cohorts without missingness included, the more accurate the results compared to "benchmark" results. In conclusion, we generally recommend the Safe Approach, a straightforward and non-inflated approach, to handle heterogeneity among cohorts in the LRS based genome-wide interaction meta-analyses.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Interacción Gen-Ambiente / Factores de Riesgo Cardiometabólico / Hipertensión / Obesidad Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Interacción Gen-Ambiente / Factores de Riesgo Cardiometabólico / Hipertensión / Obesidad Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos