Life course adiposity and amyotrophic lateral sclerosis: a Mendelian randomization study

Life course adiposity and amyotrophic lateral sclerosis: a Mendelian randomization study:

Abstract

Objectives

Observational studies have indicated that life course adiposity is associated with amyotrophic lateral sclerosis (ALS). However, whether such an association reflects causality remains unclear. We aimed to determine whether life course adiposity, such as birth weight (BW), childhood body mass index (BMI), adult BMI, body fat percentage (BF%), and waist‐to‐hip ratio (WHR), have causal effects on ALS.

Methods

Single nucleotide polymorphisms (SNPs) significantly associated with life course adiposity were used as instrumental variables to estimate the causal effects on ALS. We used summary‐level data from a cohort of 20,806 cases and 59,804 controls in a Mendelian randomization (MR) framework.

Results

Genetically predicted 1‐SD increase in BF% was associated with lower risk of ALS (odds ratio = 0.67, 95% confidence interval (CI): 0.54, 0.83; P = 3.25E‐04) after Bonferroni correction (P<0.05/5). Genetically predicted 1‐SD higher childhood BMI was suggestively associated with lower risk of ALS (0.88, 0.78 to 0.99; P=0.031). The weighted median method indicated a suggestive association between BMI and ALS (0.86, 0.69 to 0.96, P=0.016). Neither a genetically predicted 1‐SD increase in BW (IVW, 1.01, 0.87 to 1.17; P=0.939) nor WHRadjBMI (IVW, 0.90, 0.76 to 1.05, P=0.178) was associated with ALS.

Interpretation

Our findings provide novel evidence supporting a causal role of higher adiposity, taken as a whole, on lower risk of ALS. A deeper understanding of the energy metabolism of ALS is more likely to identify feasible nutritional interventions and even novel therapeutic targets that might improve the survival of ALS patients.

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