Literature DB >> 32329357

Keratinous biomarker of mercury exposure associated with amyotrophic lateral sclerosis risk in a nationwide U.S. study.

Angeline S Andrew1, Katie M O'Brien2, Brian P Jackson3, Dale P Sandler2, Wendy E Kaye4, Laurie Wagner4, Elijah W Stommel1, D Kevin Horton5, Paul Mehta5, Clarice R Weinberg2.   

Abstract

Objective: The majority of cases of the fatal neurodegenerative disease amyotrophic lateral sclerosis (ALS) are of unknown etiology. A proportion of these cases are likely to be attributable to contaminant exposures, although the specific environmental etiology of ALS remains largely a mystery. Certain forms of the neurotoxic metal mercury readily cross into the central nervous system. Fish is a dietary source of methylmercury, but also of beneficial components, such as omega-3 polyunsaturated fatty acids. Prior work using clinic-based studies of toenails and hair as keratinous biomarkers of exposure suggest elevated mercury levels in ALS patients compared with controls. We sought to validate this relationship in a U.S. case-control comparison of mercury levels in nail clippings.
Methods: We performed trace element analysis using inductively coupled plasma mass spectrometry (ICP-MS) on the nail clippings of n = 70 female, geographically representative ALS patients from the National ALS Biorepository and compared them to n = 210 age-matched controls from a set of n = 1216 nationally distributed controls from the Sister and Two Sister Studies.
Results: Compared to the lowest quartile of nail mercury, moderate levels were associated with decreased risk of ALS (P = 4.18e-6). However, the odds of having nail mercury levels above the 90th percentile were 2.3-fold higher among ALS patients compared with controls (odds ratio (OR) = 2.3, 95% confidence interval 1.10-4.58, adjusted for age and smoking status).
Conclusion: This finding suggests that excessive mercury exposure may be associated with the neurodegenerative health of aging populations.

Entities:  

Keywords:  ALS; Biomarker; U.S.; amyotrophic lateral sclerosis; keratin; mercury; nail

Year:  2020        PMID: 32329357      PMCID: PMC7483924          DOI: 10.1080/21678421.2020.1753777

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Frontotemporal Degener        ISSN: 2167-8421            Impact factor:   4.092


  42 in total

1.  The sva package for removing batch effects and other unwanted variation in high-throughput experiments.

Authors:  Jeffrey T Leek; W Evan Johnson; Hilary S Parker; Andrew E Jaffe; John D Storey
Journal:  Bioinformatics       Date:  2012-01-17       Impact factor: 6.937

2.  Fertility drugs and young-onset breast cancer: results from the Two Sister Study.

Authors:  Chunyuan Fei; Lisa A Deroo; Dale P Sandler; Clarice R Weinberg
Journal:  J Natl Cancer Inst       Date:  2012-07-06       Impact factor: 13.506

3.  Toenail mercury Levels are associated with amyotrophic lateral sclerosis risk.

Authors:  Angeline S Andrew; Celia Y Chen; Tracie A Caller; Rup Tandan; Patricia L Henegan; Brian P Jackson; Brenda P Hall; Walter G Bradley; Elijah W Stommel
Journal:  Muscle Nerve       Date:  2018-01-04       Impact factor: 3.217

4.  Toenail mercury and dietary fish consumption.

Authors:  Judy R Rees; Stefan Sturup; Celia Chen; Carol Folt; Margaret R Karagas
Journal:  J Expo Sci Environ Epidemiol       Date:  2006-08-16       Impact factor: 5.563

Review 5.  Mechanisms of mercury disposition in the body.

Authors:  Thomas W Clarkson; Jayesh B Vyas; Nazzareno Ballatori
Journal:  Am J Ind Med       Date:  2007-10       Impact factor: 2.214

6.  Comparison of hair with nail as index media for biological monitoring of mercury.

Authors:  T Suzuki; S Watanabe; N Matsuo
Journal:  Sangyo Igaku       Date:  1989-07

Review 7.  Decoding ALS: from genes to mechanism.

Authors:  J Paul Taylor; Robert H Brown; Don W Cleveland
Journal:  Nature       Date:  2016-11-10       Impact factor: 49.962

8.  Evidence for interactions between intracellular calcium stores during methylmercury-induced intracellular calcium dysregulation in rat cerebellar granule neurons.

Authors:  Tobi L Limke; James K L Otero-Montañez; William D Atchison
Journal:  J Pharmacol Exp Ther       Date:  2003-03       Impact factor: 4.030

9.  Environmental exposure to trace elements and risk of amyotrophic lateral sclerosis: a population-based case-control study.

Authors:  Margherita Bergomi; Marco Vinceti; Grazia Nacci; Vladimiro Pietrini; Peter Brätter; Dorothea Alber; Angela Ferrari; Luciano Vescovi; Donata Guidetti; Patrizia Sola; Susanna Malagu; Chiara Aramini; Gianfranco Vivoli
Journal:  Environ Res       Date:  2002-06       Impact factor: 6.498

Review 10.  Environmental mercury and its toxic effects.

Authors:  Kevin M Rice; Ernest M Walker; Miaozong Wu; Chris Gillette; Eric R Blough
Journal:  J Prev Med Public Health       Date:  2014-03-31
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  3 in total

1.  Amyotrophic Lateral Sclerosis Risk, Family Income, and Fish Consumption Estimates of Mercury and Omega-3 PUFAs in the United States.

Authors:  Hannah I Hoffman; Walter G Bradley; Celia Y Chen; Erik P Pioro; Elijah W Stommel; Angeline S Andrew
Journal:  Int J Environ Res Public Health       Date:  2021-04-24       Impact factor: 3.390

Review 2.  A perspective on persistent toxicants in veterans and amyotrophic lateral sclerosis: identifying exposures determining higher ALS risk.

Authors:  Diane B Re; Beizhan Yan; Lilian Calderón-Garcidueñas; Angeline S Andrew; Maeve Tischbein; Elijah W Stommel
Journal:  J Neurol       Date:  2022-01-01       Impact factor: 6.682

Review 3.  Oxidative Stress in Amyotrophic Lateral Sclerosis: Synergy of Genetic and Environmental Factors.

Authors:  Anca Motataianu; Georgiana Serban; Laura Barcutean; Rodica Balasa
Journal:  Int J Mol Sci       Date:  2022-08-19       Impact factor: 6.208

  3 in total

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