Associations of arsenic exposure and arsenic metabolism with the risk of non-alcoholic fatty liver disease
Growing evidences supported that arsenic exposure contributes to non-alcoholic fatty liver disease (NAFLD) risk, but findings were still inconsistent. Additionally, once absorbed, arsenic is methylated into monomethyl and dimethyl arsenicals. However, no studies investigated the association of arsen...
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description | Growing evidences supported that arsenic exposure contributes to non-alcoholic fatty liver disease (NAFLD) risk, but findings were still inconsistent. Additionally, once absorbed, arsenic is methylated into monomethyl and dimethyl arsenicals. However, no studies investigated the association of arsenic metabolism with NAFLD. Our objectives were to evaluate the associations of arsenic exposure and arsenic metabolism with NAFLD prevalence. We conducted a case-control study with 1790 participants derived from Dongfeng-Tongji cohort and measured arsenic species (arsenite, arsenate, monomethylarsonate [MMA], dimethylarsinate [DMA], and arsenobetaine) in urine. Arsenic exposure (∑As) was defined as the sum of inorganic arsenic (iAs), MMA, and DMA. Arsenic metabolism was evaluated as the proportions of inorganic-related species (iAs%, MMA%, and DMA%) and methylation efficiency ratios (primary methylation index [PMI], secondary methylation index [SMI]). NAFLD was diagnosed by liver ultrasound. Logistic regression was used to evaluate the associations. The median of ∑As was 13.24 μg/g creatinine. The ∑As showed positive and nonlinear association with moderate/severe NAFLD (OR: per log-SD = 1.33, 95% CI: [1.03,1.71]; Pfor nonlinearity = 0.021). The iAs% (OR: per SD = 1.16, 95% CI: [1.03,1.30]) and SMI (OR: per log-SD = 1.16, 95% CI: [1.03,1.31]) showed positive while MMA% (OR: per SD = 0.80, 95% CI: [0.70,0.91]) and PMI (OR: per log-SD = 0.86, 95% CI: [0.77,0.96]) showed inverse associations with NAFLD. Moreover, the ORs (95% CI) of NAFLD for each 5% increase in iAs% was 1.36 (1.17,1.58) when MMA% decreased and 1.07 (1.01,1.13) when DMA% decreased; and for each 5% increase in MMA%, it was 0.74 (0.63,0.86) and 0.79 (0.69,0.91) when iAs% and DMA% decreased, respectively. The results suggest that inorganic arsenic exposure is positively associated with NAFLD risk and arsenic methylation efficiency plays a role in the NAFLD. The findings provide clues to explore potential interventions for the prevention of NAFLD. Prospective studies are needed to validate our findings. |
doi_str_mv | 10.1016/j.ijheh.2024.114342 |
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Additionally, once absorbed, arsenic is methylated into monomethyl and dimethyl arsenicals. However, no studies investigated the association of arsenic metabolism with NAFLD. Our objectives were to evaluate the associations of arsenic exposure and arsenic metabolism with NAFLD prevalence. We conducted a case-control study with 1790 participants derived from Dongfeng-Tongji cohort and measured arsenic species (arsenite, arsenate, monomethylarsonate [MMA], dimethylarsinate [DMA], and arsenobetaine) in urine. Arsenic exposure (∑As) was defined as the sum of inorganic arsenic (iAs), MMA, and DMA. Arsenic metabolism was evaluated as the proportions of inorganic-related species (iAs%, MMA%, and DMA%) and methylation efficiency ratios (primary methylation index [PMI], secondary methylation index [SMI]). NAFLD was diagnosed by liver ultrasound. Logistic regression was used to evaluate the associations. The median of ∑As was 13.24 μg/g creatinine. The ∑As showed positive and nonlinear association with moderate/severe NAFLD (OR: per log-SD = 1.33, 95% CI: [1.03,1.71]; Pfor nonlinearity = 0.021). The iAs% (OR: per SD = 1.16, 95% CI: [1.03,1.30]) and SMI (OR: per log-SD = 1.16, 95% CI: [1.03,1.31]) showed positive while MMA% (OR: per SD = 0.80, 95% CI: [0.70,0.91]) and PMI (OR: per log-SD = 0.86, 95% CI: [0.77,0.96]) showed inverse associations with NAFLD. Moreover, the ORs (95% CI) of NAFLD for each 5% increase in iAs% was 1.36 (1.17,1.58) when MMA% decreased and 1.07 (1.01,1.13) when DMA% decreased; and for each 5% increase in MMA%, it was 0.74 (0.63,0.86) and 0.79 (0.69,0.91) when iAs% and DMA% decreased, respectively. The results suggest that inorganic arsenic exposure is positively associated with NAFLD risk and arsenic methylation efficiency plays a role in the NAFLD. The findings provide clues to explore potential interventions for the prevention of NAFLD. Prospective studies are needed to validate our findings.</description><identifier>ISSN: 1438-4639</identifier><identifier>EISSN: 1618-131X</identifier><identifier>DOI: 10.1016/j.ijheh.2024.114342</identifier><identifier>PMID: 38401403</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Arsenic ; Metabolism ; Non-alcoholic fatty liver disease</subject><ispartof>International journal of hygiene and environmental health, 2024-04, Vol.257, p.114342-114342, Article 114342</ispartof><rights>2024 Elsevier GmbH</rights><rights>Copyright © 2024 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-d8332990c13babf423175528093173da464be9925b96747df3e181d6ff4037ed3</citedby><cites>FETCH-LOGICAL-c359t-d8332990c13babf423175528093173da464be9925b96747df3e181d6ff4037ed3</cites><orcidid>0000-0002-4634-8251 ; 0000-0002-2096-921X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1438463924000233$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38401403$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yuenan</creatorcontrib><creatorcontrib>Li, Weiya</creatorcontrib><creatorcontrib>Zhang, Jiazhen</creatorcontrib><creatorcontrib>Yan, Yan</creatorcontrib><creatorcontrib>Zhou, Qihang</creatorcontrib><creatorcontrib>Liu, Qianying</creatorcontrib><creatorcontrib>Guan, Youbin</creatorcontrib><creatorcontrib>Zhao, Zhuoya</creatorcontrib><creatorcontrib>An, Jun</creatorcontrib><creatorcontrib>Cheng, Xu</creatorcontrib><creatorcontrib>He, Meian</creatorcontrib><title>Associations of arsenic exposure and arsenic metabolism with the risk of non-alcoholic fatty liver disease</title><title>International journal of hygiene and environmental health</title><addtitle>Int J Hyg Environ Health</addtitle><description>Growing evidences supported that arsenic exposure contributes to non-alcoholic fatty liver disease (NAFLD) risk, but findings were still inconsistent. Additionally, once absorbed, arsenic is methylated into monomethyl and dimethyl arsenicals. However, no studies investigated the association of arsenic metabolism with NAFLD. Our objectives were to evaluate the associations of arsenic exposure and arsenic metabolism with NAFLD prevalence. We conducted a case-control study with 1790 participants derived from Dongfeng-Tongji cohort and measured arsenic species (arsenite, arsenate, monomethylarsonate [MMA], dimethylarsinate [DMA], and arsenobetaine) in urine. Arsenic exposure (∑As) was defined as the sum of inorganic arsenic (iAs), MMA, and DMA. Arsenic metabolism was evaluated as the proportions of inorganic-related species (iAs%, MMA%, and DMA%) and methylation efficiency ratios (primary methylation index [PMI], secondary methylation index [SMI]). NAFLD was diagnosed by liver ultrasound. Logistic regression was used to evaluate the associations. The median of ∑As was 13.24 μg/g creatinine. The ∑As showed positive and nonlinear association with moderate/severe NAFLD (OR: per log-SD = 1.33, 95% CI: [1.03,1.71]; Pfor nonlinearity = 0.021). The iAs% (OR: per SD = 1.16, 95% CI: [1.03,1.30]) and SMI (OR: per log-SD = 1.16, 95% CI: [1.03,1.31]) showed positive while MMA% (OR: per SD = 0.80, 95% CI: [0.70,0.91]) and PMI (OR: per log-SD = 0.86, 95% CI: [0.77,0.96]) showed inverse associations with NAFLD. Moreover, the ORs (95% CI) of NAFLD for each 5% increase in iAs% was 1.36 (1.17,1.58) when MMA% decreased and 1.07 (1.01,1.13) when DMA% decreased; and for each 5% increase in MMA%, it was 0.74 (0.63,0.86) and 0.79 (0.69,0.91) when iAs% and DMA% decreased, respectively. The results suggest that inorganic arsenic exposure is positively associated with NAFLD risk and arsenic methylation efficiency plays a role in the NAFLD. The findings provide clues to explore potential interventions for the prevention of NAFLD. Prospective studies are needed to validate our findings.</description><subject>Arsenic</subject><subject>Metabolism</subject><subject>Non-alcoholic fatty liver disease</subject><issn>1438-4639</issn><issn>1618-131X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE9v1DAQxS0EoqXwCZCQj1yyeGznjw8cqqpQpEpcQOJmOfZEcUjixeNt6bcny5YeOc1o5r15mh9jb0HsQEDzYdrFacRxJ4XUOwCttHzGzqGBrgIFP55vvVZdpRtlztgrokkICaIzL9mZ6rQALdQ5my6Jko-uxLQSTwN3mXCNnuPvfaJDRu7W8DRcsLg-zZEWfh_LyMuIPEf6eTSuaa3c7NO47T0fXCkPfI53mHmIhI7wNXsxuJnwzWO9YN8_XX-7uqluv37-cnV5W3lVm1KFTilpjPCgetcPWipo61p2wmyNCk43ukdjZN2bptVtGBRCB6EZhu2hFoO6YO9Pd_c5_TogFbtE8jjPbsV0ICtN3ULTAshNqk5SnxNRxsHuc1xcfrAg7BGynexfyPYI2Z4gb653jwGHfsHw5PlHdRN8PAlwe_MuYrbkI64eQ8zoiw0p_jfgD5p-js0</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Liu, Yuenan</creator><creator>Li, Weiya</creator><creator>Zhang, Jiazhen</creator><creator>Yan, Yan</creator><creator>Zhou, Qihang</creator><creator>Liu, Qianying</creator><creator>Guan, Youbin</creator><creator>Zhao, Zhuoya</creator><creator>An, Jun</creator><creator>Cheng, Xu</creator><creator>He, Meian</creator><general>Elsevier GmbH</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4634-8251</orcidid><orcidid>https://orcid.org/0000-0002-2096-921X</orcidid></search><sort><creationdate>202404</creationdate><title>Associations of arsenic exposure and arsenic metabolism with the risk of non-alcoholic fatty liver disease</title><author>Liu, Yuenan ; Li, Weiya ; Zhang, Jiazhen ; Yan, Yan ; Zhou, Qihang ; Liu, Qianying ; Guan, Youbin ; Zhao, Zhuoya ; An, Jun ; Cheng, Xu ; He, Meian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-d8332990c13babf423175528093173da464be9925b96747df3e181d6ff4037ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Arsenic</topic><topic>Metabolism</topic><topic>Non-alcoholic fatty liver disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yuenan</creatorcontrib><creatorcontrib>Li, Weiya</creatorcontrib><creatorcontrib>Zhang, Jiazhen</creatorcontrib><creatorcontrib>Yan, Yan</creatorcontrib><creatorcontrib>Zhou, Qihang</creatorcontrib><creatorcontrib>Liu, Qianying</creatorcontrib><creatorcontrib>Guan, Youbin</creatorcontrib><creatorcontrib>Zhao, Zhuoya</creatorcontrib><creatorcontrib>An, Jun</creatorcontrib><creatorcontrib>Cheng, Xu</creatorcontrib><creatorcontrib>He, Meian</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of hygiene and environmental health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yuenan</au><au>Li, Weiya</au><au>Zhang, Jiazhen</au><au>Yan, Yan</au><au>Zhou, Qihang</au><au>Liu, Qianying</au><au>Guan, Youbin</au><au>Zhao, Zhuoya</au><au>An, Jun</au><au>Cheng, Xu</au><au>He, Meian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Associations of arsenic exposure and arsenic metabolism with the risk of non-alcoholic fatty liver disease</atitle><jtitle>International journal of hygiene and environmental health</jtitle><addtitle>Int J Hyg Environ Health</addtitle><date>2024-04</date><risdate>2024</risdate><volume>257</volume><spage>114342</spage><epage>114342</epage><pages>114342-114342</pages><artnum>114342</artnum><issn>1438-4639</issn><eissn>1618-131X</eissn><abstract>Growing evidences supported that arsenic exposure contributes to non-alcoholic fatty liver disease (NAFLD) risk, but findings were still inconsistent. Additionally, once absorbed, arsenic is methylated into monomethyl and dimethyl arsenicals. However, no studies investigated the association of arsenic metabolism with NAFLD. Our objectives were to evaluate the associations of arsenic exposure and arsenic metabolism with NAFLD prevalence. We conducted a case-control study with 1790 participants derived from Dongfeng-Tongji cohort and measured arsenic species (arsenite, arsenate, monomethylarsonate [MMA], dimethylarsinate [DMA], and arsenobetaine) in urine. Arsenic exposure (∑As) was defined as the sum of inorganic arsenic (iAs), MMA, and DMA. Arsenic metabolism was evaluated as the proportions of inorganic-related species (iAs%, MMA%, and DMA%) and methylation efficiency ratios (primary methylation index [PMI], secondary methylation index [SMI]). NAFLD was diagnosed by liver ultrasound. Logistic regression was used to evaluate the associations. The median of ∑As was 13.24 μg/g creatinine. The ∑As showed positive and nonlinear association with moderate/severe NAFLD (OR: per log-SD = 1.33, 95% CI: [1.03,1.71]; Pfor nonlinearity = 0.021). The iAs% (OR: per SD = 1.16, 95% CI: [1.03,1.30]) and SMI (OR: per log-SD = 1.16, 95% CI: [1.03,1.31]) showed positive while MMA% (OR: per SD = 0.80, 95% CI: [0.70,0.91]) and PMI (OR: per log-SD = 0.86, 95% CI: [0.77,0.96]) showed inverse associations with NAFLD. Moreover, the ORs (95% CI) of NAFLD for each 5% increase in iAs% was 1.36 (1.17,1.58) when MMA% decreased and 1.07 (1.01,1.13) when DMA% decreased; and for each 5% increase in MMA%, it was 0.74 (0.63,0.86) and 0.79 (0.69,0.91) when iAs% and DMA% decreased, respectively. The results suggest that inorganic arsenic exposure is positively associated with NAFLD risk and arsenic methylation efficiency plays a role in the NAFLD. The findings provide clues to explore potential interventions for the prevention of NAFLD. Prospective studies are needed to validate our findings.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>38401403</pmid><doi>10.1016/j.ijheh.2024.114342</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4634-8251</orcidid><orcidid>https://orcid.org/0000-0002-2096-921X</orcidid></addata></record> |
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subjects | Arsenic Metabolism Non-alcoholic fatty liver disease |
title | Associations of arsenic exposure and arsenic metabolism with the risk of non-alcoholic fatty liver disease |
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