Literature DB >> 12117651

Family correlations of arsenic methylation patterns in children and parents exposed to high concentrations of arsenic in drinking water.

Joyce S Chung1, David A Kalman, Lee E Moore, Michael J Kosnett, Alex P Arroyo, Martin Beeris, D N Guha Mazumder, Alexandra L Hernandez, Allan H Smith.   

Abstract

We investigated the evidence of a familial contribution to urinary methylation patterns in families ingesting arsenic in drinking water. Arsenic methylation can be assessed by measuring urinary levels of inorganic arsenic (InAs) and its methylated metabolites, monomethylarsonate (MMA), and dimethylarsinate (DMA). Methylation activity is reflected in the ratios: InAs/methylated arsenic (InAs/metAs) and MMA/DMA. Eleven families from Chile were selected because of their long-term exposure to very high levels of arsenic in drinking water (735-762 microg/L). Each family consisted of a father, a mother, and two children. We measured urinary arsenic and its methylated metabolites for each participant (n = 44). The intraclass correlation coefficients showed that 13-52% of the variations in the methylation patterns were from being a member of a specific family. Family correlations were calculated for father-mother, parent-child, and sibling-sibling pairs. Methylation patterns correlated strongly between siblings [r = 0.78 for InAs/metAs, 95% confidence interval (CI), 0.34-0.94; r = 0.82 for MMA/DMA, 95%CI, 0.43-0.95] compared to lower correlations in father-mother pairs (r = 0.18, r = -0.01, respectively), after adjustment for total urinary arsenic, age, and sex. Family correlations were not notably altered when adjustments were made for specific blood micronutrients (methionine, homocysteine, folate, vitamin B6, selenium, and vitamin B12 potentially related to methylation. We also report on a family pedigree with high prevalence of arsenic-induced effects. Participants from this family had low InAs/metAs values, which is consistent with increased toxicity of trivalent methylated arsenic species. Despite our small sample size, we observed that methylation patterns aggregate in families and are correlated in siblings, providing evidence of a genetic basis for the variation in arsenic methylation. Larger studies with more extensive pedigrees will need to be conducted to confirm these findings.

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Year:  2002        PMID: 12117651      PMCID: PMC1240920          DOI: 10.1289/ehp.02110729

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  24 in total

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2.  Methylated trivalent arsenic species are genotoxic.

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Journal:  Chem Res Toxicol       Date:  2001-04       Impact factor: 3.739

3.  Correlation of erythrocyte catechol-O-methyltransferase activity between siblings.

Authors:  R M Weinshilboum; F A Raymond; L R Elveback; W H Weidman
Journal:  Nature       Date:  1974-12-06       Impact factor: 49.962

4.  Atherogenicity and carcinogenicity of high-arsenic artesian well water. Multiple risk factors and related malignant neoplasms of blackfoot disease.

Authors:  C J Chen; M M Wu; S S Lee; J D Wang; S H Cheng; H Y Wu
Journal:  Arteriosclerosis       Date:  1988 Sep-Oct

5.  Pharmacogenetics of N-methylation: heritability of human erythrocyte histamine N-methyltransferase activity.

Authors:  M C Scott; J A Van Loon; R M Weinshilboum
Journal:  Clin Pharmacol Ther       Date:  1988-03       Impact factor: 6.875

6.  Relationship of urinary arsenic to intake estimates and a biomarker of effect, bladder cell micronuclei.

Authors:  M L Biggs; D A Kalman; L E Moore; C Hopenhayn-Rich; M T Smith; A H Smith
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Authors:  M Vahter
Journal:  Sci Prog       Date:  1999       Impact factor: 2.774

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Authors:  M Styblo; L M Del Razo; L Vega; D R Germolec; E L LeCluyse; G A Hamilton; W Reed; C Wang; W R Cullen; D J Thomas
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Journal:  Clin Neurol Neurosurg       Date:  1992       Impact factor: 1.876

10.  Arsenic-induced skin lesions among Atacameño people in Northern Chile despite good nutrition and centuries of exposure.

Authors:  A H Smith; A P Arroyo; D N Mazumder; M J Kosnett; A L Hernandez; M Beeris; M M Smith; L E Moore
Journal:  Environ Health Perspect       Date:  2000-07       Impact factor: 9.031

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  33 in total

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2.  Indigenous American ancestry is associated with arsenic methylation efficiency in an admixed population of northwest Mexico.

Authors:  Paulina Gomez-Rubio; Yann C Klimentidis; Ernesto Cantu-Soto; Maria M Meza-Montenegro; Dean Billheimer; Zhenqiang Lu; Zhao Chen; Walter T Klimecki
Journal:  J Toxicol Environ Health A       Date:  2012

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Review 4.  Arsenic exposure in Latin America: biomarkers, risk assessments and related health effects.

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6.  Developmental and genetic modulation of arsenic biotransformation: a gene by environment interaction?

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7.  Individual differences in arsenic metabolism and lung cancer in a case-control study in Cordoba, Argentina.

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8.  Arsenic methylation and lung and bladder cancer in a case-control study in northern Chile.

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9.  Variations in arsenic methylation capacity and oxidative DNA lesions over a 2-year period in a high arsenic-exposed population.

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10.  Decreased urinary beta-defensin-1 expression as a biomarker of response to arsenic.

Authors:  Christine M Hegedus; Christine F Skibola; Marcella Warner; Danica R Skibola; David Alexander; Sophia Lim; Nygerma L Dangleben; Luoping Zhang; Michael Clark; Ruth M Pfeiffer; Craig Steinmaus; Allan H Smith; Martyn T Smith; Lee E Moore
Journal:  Toxicol Sci       Date:  2008-05-28       Impact factor: 4.849

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