Assessing causality in the association between attention-deficit/hyperactivity disorder and obesity: a Mendelian randomization study

被引:34
|
作者
Martins-Silva, Thais [1 ]
Vaz, Juliana dos Santos [1 ,2 ]
Hutz, Mara Helena [3 ]
Salatino-Oliveira, Angelica [3 ]
Genro, Julia Pasqualini [4 ]
Hartwig, Fernando Pires [1 ,5 ]
Moreira-Maia, Carlos Renato [6 ]
Rohde, Luis Augusto [6 ,7 ]
Borges, Maria Carolina [5 ,8 ]
Tovo-Rodrigues, Luciana [1 ]
机构
[1] Univ Fed Pelotas, Postgrad Program Epidemiol, Pelotas, RS, Brazil
[2] Univ Fed Pelotas, Fac Nutr, Pelotas, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Postgrad Program Genet & Mol Biol, Porto Alegre, RS, Brazil
[4] Univ Fundacao Ciencias Saude Porto Alegre, Postgrad Program Biosci, Porto Alegre, RS, Brazil
[5] Univ Bristol, Integrat Epidemiol Unit, MRC, Bristol, Avon, England
[6] Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Dept Psychiat, Porto Alegre, RS, Brazil
[7] Natl Inst Dev Psychiat Children & Adolescents, Sao Paulo, SP, Brazil
[8] Univ Bristol, Bristol Med Sch, Populat Hlth Sci, Bristol, Avon, England
基金
英国医学研究理事会;
关键词
DEFICIT HYPERACTIVITY DISORDER; BODY-MASS INDEX; ADHD; RISK; ADOLESCENTS; SYMPTOMS; ALLELES; HEALTH; SAMPLE;
D O I
10.1038/s41366-019-0346-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Objectives Attention-deficit hyperactivity disorder (ADHD), one of the most common neurodevelopmental disorders in childhood and adolescence, is associated with obesity in observational studies. However, it is unclear whether ADHD contributes to, results from or is merely correlated with obesity. This study evaluates the presence and direction of a causal effect between ADHD and obesity. Subjects/Methods We performed a bidirectional two-sample Mendelian randomization using summary data from consortia of genome-wide association studies to investigate if ADHD (N = 55,374) has a causal effect on body mass index (BMI) in childhood (N = 35,668) and adulthood (N = 322,154-500,000), and vice-versa. The main analysis was performed using the inverse variance weighted (IVW) method. As sensitivity analyses, we used other Mendelian randomization methods that are more robust to horizontal pleiotropy (i.e., MR-Egger, weighted mode, and penalized weighted median estimators), as well as stratified the analysis by the putative mechanisms of genetic instruments (i.e., pathways involved or not in neurological processes). Results The IVW method indicated a positive causal effect of BMI on ADHD: beta = 0.324 (95% CI 0.198 to 0.449, p < 0.001; expressed as change in ln(odds ratio) of ADHD per each additional SD unit of BMI). IVW estimates were directionally consistent with other methods. On the other hand, we did not find consistent evidence for a causal effect of ADHD genetic liability on BMI. Conclusions The results suggested that higher BMI increases the risk of developing ADHD, but not the other way around.
引用
收藏
页码:2500 / 2508
页数:9
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