Cargando…
Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India
IMPORTANCE: Arsenic, a contaminant of groundwater and irrigated crops, is a global public health hazard. Exposure to low levels of arsenic through food extends well beyond the areas with high arsenic content in water. OBJECTIVE: To identify cognitive impairments following commonly prevalent low-leve...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Medical Association
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10182429/ https://www.ncbi.nlm.nih.gov/pubmed/37171822 http://dx.doi.org/10.1001/jamanetworkopen.2023.12810 |
_version_ | 1785041765143674880 |
---|---|
author | Vaidya, Nilakshi Holla, Bharath Heron, Jon Sharma, Eesha Zhang, Yuning Fernandes, Gwen Iyengar, Udita Spiers, Alex Yadav, Anupa Das, Surajit Roy, Sanjit Ahuja, Chirag K. Barker, Gareth J. Basu, Debasish Bharath, Rose Dawn Hickman, Matthew Jain, Sanjeev Kalyanram, Kartik Kartik, Kamakshi Krishna, Murali Krishnaveni, Ghattu Kumaran, Kalyanaraman Kuriyan, Rebecca Murthy, Pratima Papadopoulos Orfanos, Dimitri Purushottam, Meera Kurpad, Sunita Simon Singh, Lenin Singh, Roshan Subodh, B. N. Toledano, Mireille Walter, Henrik Desrivières, Sylvane Chakrabarti, Amit Benegal, Vivek Schumann, Gunter |
author_facet | Vaidya, Nilakshi Holla, Bharath Heron, Jon Sharma, Eesha Zhang, Yuning Fernandes, Gwen Iyengar, Udita Spiers, Alex Yadav, Anupa Das, Surajit Roy, Sanjit Ahuja, Chirag K. Barker, Gareth J. Basu, Debasish Bharath, Rose Dawn Hickman, Matthew Jain, Sanjeev Kalyanram, Kartik Kartik, Kamakshi Krishna, Murali Krishnaveni, Ghattu Kumaran, Kalyanaraman Kuriyan, Rebecca Murthy, Pratima Papadopoulos Orfanos, Dimitri Purushottam, Meera Kurpad, Sunita Simon Singh, Lenin Singh, Roshan Subodh, B. N. Toledano, Mireille Walter, Henrik Desrivières, Sylvane Chakrabarti, Amit Benegal, Vivek Schumann, Gunter |
author_sort | Vaidya, Nilakshi |
collection | PubMed |
description | IMPORTANCE: Arsenic, a contaminant of groundwater and irrigated crops, is a global public health hazard. Exposure to low levels of arsenic through food extends well beyond the areas with high arsenic content in water. OBJECTIVE: To identify cognitive impairments following commonly prevalent low-level arsenic exposure and characterize their underlying brain mechanisms. DESIGN, SETTING, AND PARTICIPANTS: This multicenter population-based cohort study analyzed cross-sectional data of the Indian Consortium on Vulnerability to Externalizing Disorders and Addictions (cVEDA) cohort, recruited between November 4, 2016, and May 4, 2019. Participants aged 6 to 23 years were characterized using deep phenotyping measures of behavior, neuropsychology, psychopathology, brain neuroimaging, and exposure to developmental adversities and environmental neurotoxins. All analyses were performed between June 1, 2020, and December 31, 2021. EXPOSURE: Arsenic levels were measured in urine as an index of exposure. MAIN OUTCOMES AND MEASURES: Executive function measured using the cVEDA neuropsychological battery, gray matter volume (GMV) from T1-weighted magnetic resonance imaging, and functional network connectivity measures from resting state functional magnetic resonance imaging. RESULTS: A total of 1014 participants aged 6 to 23 years (589 male [58.1%]; mean [SD] age, 14.86 [4.79] years) were included from 5 geographic locations. Sparse-partial least squares analysis was used to describe a negative association of arsenic exposure with executive function (r = −0.12 [P = 5.4 × 10(−4)]), brain structure (r = −0.20 [P = 1.8 × 10(−8)]), and functional connectivity (within network, r = −0.12 [P = 7.5 × 10(−4)]; between network, r = −0.23 [P = 1.8 × 10(−10)]). Alterations in executive function were partially mediated by GMV (b = −0.004 [95% CI, −0.007 to −0.002]) and within-network functional connectivity (b = −0.004 [95% CI, −0.008 to −0.002]). Socioeconomic status and body mass index moderated the association between arsenic and GMV, such that the association was strongest in participants with lower socioeconomic status and body mass index. CONCLUSIONS AND RELEVANCE: The findings of this cross-sectional study suggest that low-level arsenic exposure was associated with alterations in executive functioning and underlying brain correlates. These results indicate potential detrimental consequences of arsenic exposure that are below the currently recommended guidelines and may extend beyond endemic risk areas. Precision medicine approaches to study global mental health vulnerabilities highlight widespread but potentially modifiable risk factors and a mechanistic understanding of the impact of low-level arsenic exposure on brain development. |
format | Online Article Text |
id | pubmed-10182429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-101824292023-05-14 Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India Vaidya, Nilakshi Holla, Bharath Heron, Jon Sharma, Eesha Zhang, Yuning Fernandes, Gwen Iyengar, Udita Spiers, Alex Yadav, Anupa Das, Surajit Roy, Sanjit Ahuja, Chirag K. Barker, Gareth J. Basu, Debasish Bharath, Rose Dawn Hickman, Matthew Jain, Sanjeev Kalyanram, Kartik Kartik, Kamakshi Krishna, Murali Krishnaveni, Ghattu Kumaran, Kalyanaraman Kuriyan, Rebecca Murthy, Pratima Papadopoulos Orfanos, Dimitri Purushottam, Meera Kurpad, Sunita Simon Singh, Lenin Singh, Roshan Subodh, B. N. Toledano, Mireille Walter, Henrik Desrivières, Sylvane Chakrabarti, Amit Benegal, Vivek Schumann, Gunter JAMA Netw Open Original Investigation IMPORTANCE: Arsenic, a contaminant of groundwater and irrigated crops, is a global public health hazard. Exposure to low levels of arsenic through food extends well beyond the areas with high arsenic content in water. OBJECTIVE: To identify cognitive impairments following commonly prevalent low-level arsenic exposure and characterize their underlying brain mechanisms. DESIGN, SETTING, AND PARTICIPANTS: This multicenter population-based cohort study analyzed cross-sectional data of the Indian Consortium on Vulnerability to Externalizing Disorders and Addictions (cVEDA) cohort, recruited between November 4, 2016, and May 4, 2019. Participants aged 6 to 23 years were characterized using deep phenotyping measures of behavior, neuropsychology, psychopathology, brain neuroimaging, and exposure to developmental adversities and environmental neurotoxins. All analyses were performed between June 1, 2020, and December 31, 2021. EXPOSURE: Arsenic levels were measured in urine as an index of exposure. MAIN OUTCOMES AND MEASURES: Executive function measured using the cVEDA neuropsychological battery, gray matter volume (GMV) from T1-weighted magnetic resonance imaging, and functional network connectivity measures from resting state functional magnetic resonance imaging. RESULTS: A total of 1014 participants aged 6 to 23 years (589 male [58.1%]; mean [SD] age, 14.86 [4.79] years) were included from 5 geographic locations. Sparse-partial least squares analysis was used to describe a negative association of arsenic exposure with executive function (r = −0.12 [P = 5.4 × 10(−4)]), brain structure (r = −0.20 [P = 1.8 × 10(−8)]), and functional connectivity (within network, r = −0.12 [P = 7.5 × 10(−4)]; between network, r = −0.23 [P = 1.8 × 10(−10)]). Alterations in executive function were partially mediated by GMV (b = −0.004 [95% CI, −0.007 to −0.002]) and within-network functional connectivity (b = −0.004 [95% CI, −0.008 to −0.002]). Socioeconomic status and body mass index moderated the association between arsenic and GMV, such that the association was strongest in participants with lower socioeconomic status and body mass index. CONCLUSIONS AND RELEVANCE: The findings of this cross-sectional study suggest that low-level arsenic exposure was associated with alterations in executive functioning and underlying brain correlates. These results indicate potential detrimental consequences of arsenic exposure that are below the currently recommended guidelines and may extend beyond endemic risk areas. Precision medicine approaches to study global mental health vulnerabilities highlight widespread but potentially modifiable risk factors and a mechanistic understanding of the impact of low-level arsenic exposure on brain development. American Medical Association 2023-05-12 /pmc/articles/PMC10182429/ /pubmed/37171822 http://dx.doi.org/10.1001/jamanetworkopen.2023.12810 Text en Copyright 2023 Vaidya N et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License. |
spellingShingle | Original Investigation Vaidya, Nilakshi Holla, Bharath Heron, Jon Sharma, Eesha Zhang, Yuning Fernandes, Gwen Iyengar, Udita Spiers, Alex Yadav, Anupa Das, Surajit Roy, Sanjit Ahuja, Chirag K. Barker, Gareth J. Basu, Debasish Bharath, Rose Dawn Hickman, Matthew Jain, Sanjeev Kalyanram, Kartik Kartik, Kamakshi Krishna, Murali Krishnaveni, Ghattu Kumaran, Kalyanaraman Kuriyan, Rebecca Murthy, Pratima Papadopoulos Orfanos, Dimitri Purushottam, Meera Kurpad, Sunita Simon Singh, Lenin Singh, Roshan Subodh, B. N. Toledano, Mireille Walter, Henrik Desrivières, Sylvane Chakrabarti, Amit Benegal, Vivek Schumann, Gunter Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India |
title | Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India |
title_full | Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India |
title_fullStr | Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India |
title_full_unstemmed | Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India |
title_short | Neurocognitive Analysis of Low-level Arsenic Exposure and Executive Function Mediated by Brain Anomalies Among Children, Adolescents, and Young Adults in India |
title_sort | neurocognitive analysis of low-level arsenic exposure and executive function mediated by brain anomalies among children, adolescents, and young adults in india |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10182429/ https://www.ncbi.nlm.nih.gov/pubmed/37171822 http://dx.doi.org/10.1001/jamanetworkopen.2023.12810 |
work_keys_str_mv | AT vaidyanilakshi neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT hollabharath neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT heronjon neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT sharmaeesha neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT zhangyuning neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT fernandesgwen neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT iyengarudita neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT spiersalex neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT yadavanupa neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT dassurajit neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT roysanjit neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT ahujachiragk neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT barkergarethj neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT basudebasish neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT bharathrosedawn neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT hickmanmatthew neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT jainsanjeev neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT kalyanramkartik neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT kartikkamakshi neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT krishnamurali neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT krishnavenighattu neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT kumarankalyanaraman neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT kuriyanrebecca neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT murthypratima neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT papadopoulosorfanosdimitri neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT purushottammeera neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT kurpadsunitasimon neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT singhlenin neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT singhroshan neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT subodhbn neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT toledanomireille neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT walterhenrik neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT desrivieressylvane neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT chakrabartiamit neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT benegalvivek neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia AT schumanngunter neurocognitiveanalysisoflowlevelarsenicexposureandexecutivefunctionmediatedbybrainanomaliesamongchildrenadolescentsandyoungadultsinindia |