Your browser doesn't support javascript.
loading
Shared familial risk for type 2 diabetes mellitus and psychiatric disorders: a nationwide multigenerational genetics study.
Wimberley, Theresa; Brikell, Isabell; Astrup, Aske; Larsen, Janne T; Petersen, Liselotte V; Albiñana, Clara; Vilhjálmsson, Bjarni J; Bulik, Cynthia M; Chang, Zheng; Fanelli, Giuseppe; Bralten, Janita; Mota, Nina R; Salas-Salvadó, Jordi; Fernandez-Aranda, Fernando; Bulló, Monica; Franke, Barbara; Børglum, Anders; Mortensen, Preben B; Horsdal, Henriette T; Dalsgaard, Søren.
Afiliação
  • Wimberley T; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Brikell I; The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Aarhus, Denmark.
  • Astrup A; Centre for Integrated Register-based Research (CIRRAU), Aarhus University, Aarhus, Denmark.
  • Larsen JT; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Petersen LV; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Albiñana C; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Vilhjálmsson BJ; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Bulik CM; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Chang Z; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Fanelli G; The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Aarhus, Denmark.
  • Bralten J; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Mota NR; The Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Aarhus, Denmark.
  • Salas-Salvadó J; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Fernandez-Aranda F; The National Centre for Register-based Research, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark.
  • Bulló M; Bioinformatics Research Centre, Aarhus University, Aarhus, Denmark.
  • Franke B; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Børglum A; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, USA.
  • Mortensen PB; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, USA.
  • Horsdal HT; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Dalsgaard S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Psychol Med ; : 1-10, 2024 May 27.
Article em En | MEDLINE | ID: mdl-38801094
ABSTRACT

BACKGROUND:

Psychiatric disorders and type 2 diabetes mellitus (T2DM) are heritable, polygenic, and often comorbid conditions, yet knowledge about their potential shared familial risk is lacking. We used family designs and T2DM polygenic risk score (T2DM-PRS) to investigate the genetic associations between psychiatric disorders and T2DM.

METHODS:

We linked 659 906 individuals born in Denmark 1990-2000 to their parents, grandparents, and aunts/uncles using population-based registers. We compared rates of T2DM in relatives of children with and without a diagnosis of any or one of 11 specific psychiatric disorders, including neuropsychiatric and neurodevelopmental disorders, using Cox regression. In a genotyped sample (iPSYCH2015) of individuals born 1981-2008 (n = 134 403), we used logistic regression to estimate associations between a T2DM-PRS and these psychiatric disorders.

RESULTS:

Among 5 235 300 relative pairs, relatives of individuals with a psychiatric disorder had an increased risk for T2DM with stronger associations for closer relatives (parentshazard ratio = 1.38, 95% confidence interval 1.35-1.42; grandparents 1.14, 1.13-1.15; and aunts/uncles 1.19, 1.16-1.22). In the genetic sample, one standard deviation increase in T2DM-PRS was associated with an increased risk for any psychiatric disorder (odds ratio = 1.11, 1.08-1.14). Both familial T2DM and T2DM-PRS were significantly associated with seven of 11 psychiatric disorders, most strongly with attention-deficit/hyperactivity disorder and conduct disorder, and inversely with anorexia nervosa.

CONCLUSIONS:

Our findings of familial co-aggregation and higher T2DM polygenic liability associated with psychiatric disorders point toward shared familial risk. This suggests that part of the comorbidity is explained by shared familial risks. The underlying mechanisms still remain largely unknown and the contributions of genetics and environment need further investigation.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Psychol Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Psychol Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Dinamarca