Cargando…

Influence of Cobalamin on Arsenic Metabolism in Bangladesh

BACKGROUND: Arsenic is a carcinogen to which 35 million people in Bangladesh are chronically exposed. The enzymatic transfer of methyl groups to inorganic As (iAs) generates monomethylarsonic (MMA) and dimethylarsinic acids (DMA) and facilitates urinary As (uAs) elimination. This process is dependen...

Descripción completa

Detalles Bibliográficos
Autores principales: Hall, Megan N., Liu, Xinhua, Slavkovich, Vesna, Ilievski, Vesna, Mi, Zhongyuan, Alam, Shafiul, Factor-Litvak, Pam, Ahsan, Habibul, Graziano, Joseph H., Gamble, Mary V.
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801198/
https://www.ncbi.nlm.nih.gov/pubmed/20049124
http://dx.doi.org/10.1289/ehp.0900734
_version_ 1782175916905988096
author Hall, Megan N.
Liu, Xinhua
Slavkovich, Vesna
Ilievski, Vesna
Mi, Zhongyuan
Alam, Shafiul
Factor-Litvak, Pam
Ahsan, Habibul
Graziano, Joseph H.
Gamble, Mary V.
author_facet Hall, Megan N.
Liu, Xinhua
Slavkovich, Vesna
Ilievski, Vesna
Mi, Zhongyuan
Alam, Shafiul
Factor-Litvak, Pam
Ahsan, Habibul
Graziano, Joseph H.
Gamble, Mary V.
author_sort Hall, Megan N.
collection PubMed
description BACKGROUND: Arsenic is a carcinogen to which 35 million people in Bangladesh are chronically exposed. The enzymatic transfer of methyl groups to inorganic As (iAs) generates monomethylarsonic (MMA) and dimethylarsinic acids (DMA) and facilitates urinary As (uAs) elimination. This process is dependent on one-carbon metabolism, a pathway in which folate and cobalamin have essential roles in the recruitment and transfer of methyl groups. Although DMA(V) is the least toxic metabolite, increasing evidence suggests that MMA(III) may be the most cytotoxic and genotoxic As intermediary metabolite. OBJECTIVE: We examined the associations between plasma cobalamin and uAs metabolites. METHODS: We conducted a cross-sectional study of 778 Bangladeshi adults in which we over-sampled cobalamin-deficient participants. Participants provided blood samples for the measurement of plasma cobalamin and urine specimens for As measurements. RESULTS: Cobalamin was inversely associated with the proportion of total uAs excreted as iAs (%iAs) [unstandardized regression coefficient (b) = –0.10; 95% confidence interval (CI), −0.17 to −0.02; p = 0.01] and positively associated with %MMA (b = 0.12; 95% CI, 0.05 to 0.20; p = 0.001). Both of these associations were stronger among folate-sufficient participants (%iAs: b = −0.17; 95% CI, −0.30 to −0.03; p = 0.02. %MMA: b = 0.20; 95% CI, 0.11 to 0.30; p < 0.0001), and the differences by folate status were statistically significant. CONCLUSIONS: In this group of Bangladeshi adults, cobalamin appeared to facilitate the first As methylation step among folate-sufficient individuals. Given the toxicity of MMA(III), our findings suggest that in contrast to folate, cobalamin may not favorably influence As metabolism.
format Text
id pubmed-2801198
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher National Institute of Environmental Health Sciences
record_format MEDLINE/PubMed
spelling pubmed-28011982010-01-04 Influence of Cobalamin on Arsenic Metabolism in Bangladesh Hall, Megan N. Liu, Xinhua Slavkovich, Vesna Ilievski, Vesna Mi, Zhongyuan Alam, Shafiul Factor-Litvak, Pam Ahsan, Habibul Graziano, Joseph H. Gamble, Mary V. Environ Health Perspect Research BACKGROUND: Arsenic is a carcinogen to which 35 million people in Bangladesh are chronically exposed. The enzymatic transfer of methyl groups to inorganic As (iAs) generates monomethylarsonic (MMA) and dimethylarsinic acids (DMA) and facilitates urinary As (uAs) elimination. This process is dependent on one-carbon metabolism, a pathway in which folate and cobalamin have essential roles in the recruitment and transfer of methyl groups. Although DMA(V) is the least toxic metabolite, increasing evidence suggests that MMA(III) may be the most cytotoxic and genotoxic As intermediary metabolite. OBJECTIVE: We examined the associations between plasma cobalamin and uAs metabolites. METHODS: We conducted a cross-sectional study of 778 Bangladeshi adults in which we over-sampled cobalamin-deficient participants. Participants provided blood samples for the measurement of plasma cobalamin and urine specimens for As measurements. RESULTS: Cobalamin was inversely associated with the proportion of total uAs excreted as iAs (%iAs) [unstandardized regression coefficient (b) = –0.10; 95% confidence interval (CI), −0.17 to −0.02; p = 0.01] and positively associated with %MMA (b = 0.12; 95% CI, 0.05 to 0.20; p = 0.001). Both of these associations were stronger among folate-sufficient participants (%iAs: b = −0.17; 95% CI, −0.30 to −0.03; p = 0.02. %MMA: b = 0.20; 95% CI, 0.11 to 0.30; p < 0.0001), and the differences by folate status were statistically significant. CONCLUSIONS: In this group of Bangladeshi adults, cobalamin appeared to facilitate the first As methylation step among folate-sufficient individuals. Given the toxicity of MMA(III), our findings suggest that in contrast to folate, cobalamin may not favorably influence As metabolism. National Institute of Environmental Health Sciences 2009-11 2009-07-31 /pmc/articles/PMC2801198/ /pubmed/20049124 http://dx.doi.org/10.1289/ehp.0900734 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Hall, Megan N.
Liu, Xinhua
Slavkovich, Vesna
Ilievski, Vesna
Mi, Zhongyuan
Alam, Shafiul
Factor-Litvak, Pam
Ahsan, Habibul
Graziano, Joseph H.
Gamble, Mary V.
Influence of Cobalamin on Arsenic Metabolism in Bangladesh
title Influence of Cobalamin on Arsenic Metabolism in Bangladesh
title_full Influence of Cobalamin on Arsenic Metabolism in Bangladesh
title_fullStr Influence of Cobalamin on Arsenic Metabolism in Bangladesh
title_full_unstemmed Influence of Cobalamin on Arsenic Metabolism in Bangladesh
title_short Influence of Cobalamin on Arsenic Metabolism in Bangladesh
title_sort influence of cobalamin on arsenic metabolism in bangladesh
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801198/
https://www.ncbi.nlm.nih.gov/pubmed/20049124
http://dx.doi.org/10.1289/ehp.0900734
work_keys_str_mv AT hallmegann influenceofcobalaminonarsenicmetabolisminbangladesh
AT liuxinhua influenceofcobalaminonarsenicmetabolisminbangladesh
AT slavkovichvesna influenceofcobalaminonarsenicmetabolisminbangladesh
AT ilievskivesna influenceofcobalaminonarsenicmetabolisminbangladesh
AT mizhongyuan influenceofcobalaminonarsenicmetabolisminbangladesh
AT alamshafiul influenceofcobalaminonarsenicmetabolisminbangladesh
AT factorlitvakpam influenceofcobalaminonarsenicmetabolisminbangladesh
AT ahsanhabibul influenceofcobalaminonarsenicmetabolisminbangladesh
AT grazianojosephh influenceofcobalaminonarsenicmetabolisminbangladesh
AT gamblemaryv influenceofcobalaminonarsenicmetabolisminbangladesh