Multiple metal exposures associate with higher amyotrophic lateral sclerosis risk and mortality independent of genetic risk and correlate to self-reported exposures: a case-control study

Author:

Jang Dae-GyuORCID,Dou John F,Koubek Emily JORCID,Teener Samuel,Zhou Lili,Bakulski Kelly M,Mukherjee Bhramar,Batterman Stuart AORCID,Feldman Eva LORCID,Goutman Stephen AORCID

Abstract

BackgroundThe pathogenesis of amyotrophic lateral sclerosis (ALS) involves both genetic and environmental factors. This study investigates associations between metal measures in plasma and urine, ALS risk and survival and exposure sources.MethodsParticipants with and without ALS from Michigan provided plasma and urine samples for metal measurement via inductively coupled plasma mass spectrometry. ORs and HRs for each metal were computed using risk and survival models. Environmental risk scores (ERS) were created to evaluate the association between exposure mixtures and ALS risk and survival and exposure source. ALS (ALS-PGS) and metal (metal-PGS) polygenic risk scores were constructed from an independent genome-wide association study and relevant literature-selected single-nucleotide polymorphisms.ResultsPlasma and urine samples from 454 ALS and 294 control participants were analysed. Elevated levels of individual metals, including copper, selenium and zinc, significantly associated with ALS risk and survival. ERS representing metal mixtures strongly associated with ALS risk (plasma, OR=2.95, CI=2.38–3.62, p<0.001; urine, OR=3.10, CI=2.43–3.97, p<0.001) and poorer ALS survival (plasma, HR=1.37, CI=1.20–1.58, p<0.001; urine, HR=1.44, CI=1.23–1.67, p<0.001). Addition of the ALS-PGS or metal-PGS did not alter the significance of metals with ALS risk and survival. Occupations with high potential of metal exposure associated with elevated ERS. Additionally, occupational and non-occupational metal exposures were associated with measured plasma and urine metals.ConclusionMetals in plasma and urine associated with increased ALS risk and reduced survival, independent of genetic risk, and correlated with occupational and non-occupational metal exposures. These data underscore the significance of metal exposure in ALS risk and progression.

Funder

University of Michigan

Richard Stravitz Foundation

Peter R. Clark Fund for ALS Research

National Cancer Institute Cancer Center Support Grant

National Institute of Neurological Disorders and Stroke

Scott L. Pranger ALS Clinic Fund

ALS Association

Dr. Randall W. Whitcomb Fund for ALS Genetics

NeuroNetwork for Emerging Therapies

Coleman Therapeutic Discovery Fund

Centers for Disease Control and Prevention

National Institute of Environmental Health Sciences

Robert and Katherine Jacobs Environmental Health Initiative

Publisher

BMJ

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