Arsenic modifies the effect of folic acid in spina bifida prevention, a large hospital-based case-control study in Bangladesh.


Journal

Environmental health : a global access science source
ISSN: 1476-069X
Titre abrégé: Environ Health
Pays: England
ID NLM: 101147645

Informations de publication

Date de publication:
03 Jun 2024
Historique:
received: 25 02 2024
accepted: 19 05 2024
medline: 4 6 2024
pubmed: 4 6 2024
entrez: 3 6 2024
Statut: epublish

Résumé

Spina bifida, a developmental malformation of the spinal cord, is associated with high rates of mortality and disability. Although folic acid-based preventive strategies have been successful in reducing rates of spina bifida, some areas continue to be at higher risk because of chemical exposures. Bangladesh has high arsenic exposures through contaminated drinking water and high rates of spina bifida. This study examines the relationships between mother's arsenic exposure, folic acid, and spina bifida risk in Bangladesh. We conducted a hospital-based case-control study at the National Institute of Neurosciences & Hospital (NINS&H) in Dhaka, Bangladesh, between December 2016 and December 2022. Cases were infants under age one year with spina bifida and further classified by a neurosurgeon and imaging. Controls were drawn from children seen at NINS&H and nearby Dhaka Shishu Hospital. Mothers reported folic acid use during pregnancy, and we assessed folate status with serum assays. Arsenic exposure was estimated in drinking water using graphite furnace atomic absorption spectrophotometry (GF-AAS) and in toenails using inductively coupled plasma mass spectrometry (ICP-MS). We used logistic regression to examine the associations between arsenic and spina bifida. We used stratified models to examine the associations between folic acid and spina bifida at different levels of arsenic exposure. We evaluated data from 294 cases of spina bifida and 163 controls. We did not find a main effect of mother's arsenic exposure on spina bifida risk. However, in stratified analyses, folic acid use was associated with lower odds of spina bifida (adjusted odds ratio [OR]: 0.50, 95% confidence interval [CI]: 0.25-1.00, p = 0.05) among women with toenail arsenic concentrations below the median value of 0.46 µg/g, and no association was seen among mothers with toenail arsenic concentrations higher than 0.46 µg/g (adjusted OR: 1.09, 95% CI: 0.52-2.29, p = 0.82). Mother's arsenic exposure modified the protective association of folic acid with spina bifida. Increased surveillance and additional preventive strategies, such as folic acid fortification and reduction of arsenic, are needed in areas of high arsenic exposure.

Sections du résumé

BACKGROUND BACKGROUND
Spina bifida, a developmental malformation of the spinal cord, is associated with high rates of mortality and disability. Although folic acid-based preventive strategies have been successful in reducing rates of spina bifida, some areas continue to be at higher risk because of chemical exposures. Bangladesh has high arsenic exposures through contaminated drinking water and high rates of spina bifida. This study examines the relationships between mother's arsenic exposure, folic acid, and spina bifida risk in Bangladesh.
METHODS METHODS
We conducted a hospital-based case-control study at the National Institute of Neurosciences & Hospital (NINS&H) in Dhaka, Bangladesh, between December 2016 and December 2022. Cases were infants under age one year with spina bifida and further classified by a neurosurgeon and imaging. Controls were drawn from children seen at NINS&H and nearby Dhaka Shishu Hospital. Mothers reported folic acid use during pregnancy, and we assessed folate status with serum assays. Arsenic exposure was estimated in drinking water using graphite furnace atomic absorption spectrophotometry (GF-AAS) and in toenails using inductively coupled plasma mass spectrometry (ICP-MS). We used logistic regression to examine the associations between arsenic and spina bifida. We used stratified models to examine the associations between folic acid and spina bifida at different levels of arsenic exposure.
RESULTS RESULTS
We evaluated data from 294 cases of spina bifida and 163 controls. We did not find a main effect of mother's arsenic exposure on spina bifida risk. However, in stratified analyses, folic acid use was associated with lower odds of spina bifida (adjusted odds ratio [OR]: 0.50, 95% confidence interval [CI]: 0.25-1.00, p = 0.05) among women with toenail arsenic concentrations below the median value of 0.46 µg/g, and no association was seen among mothers with toenail arsenic concentrations higher than 0.46 µg/g (adjusted OR: 1.09, 95% CI: 0.52-2.29, p = 0.82).
CONCLUSIONS CONCLUSIONS
Mother's arsenic exposure modified the protective association of folic acid with spina bifida. Increased surveillance and additional preventive strategies, such as folic acid fortification and reduction of arsenic, are needed in areas of high arsenic exposure.

Identifiants

pubmed: 38831396
doi: 10.1186/s12940-024-01091-1
pii: 10.1186/s12940-024-01091-1
doi:

Substances chimiques

Folic Acid 935E97BOY8
Arsenic N712M78A8G
Water Pollutants, Chemical 0
Drinking Water 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

51

Subventions

Organisme : NIMH NIH HHS
ID : T32 MH112510
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES026317
Pays : United States

Informations de copyright

© 2024. The Author(s).

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Auteurs

Chih-Fu Wei (CF)

Department of Environmental Health, Harvard T.H. Chan School of Public Health, 655 Huntington Avenue, Boston, MA, 02115, USA.

Sudipta Kumer Mukherjee (SK)

Department of Paediatric Neurosurgery, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

Sheikh Muhammad Ekramullah (SM)

Department of Paediatric Neurosurgery, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

D M Arman (DM)

Department of Paediatric Neurosurgery, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

Md Joynul Islam (MJ)

Department of Clinical Neurosurgery, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

Mubinul Azim (M)

Dhaka Shishu Hospital, Dhaka, Bangladesh.

Asifur Rahman (A)

Department of Neurosurgery, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh.

Md Nafaur Rahman (MN)

Department of Paediatric Neurosurgery, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

Md Ziauddin (M)

Department of Paediatric Neurosurgery, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

Gwen Tindula (G)

Department of Epidemiology and Population Health, Stanford University, Palo Alto, , 300 Pasteur Drive, CA, 94305, USA.

Hafiza Sultana Suchanda (HS)

Pediatric Neurosurgery Research Committee, National Institute of Neurosciences & Hospital, Sher-e-Bangla Nagar, Agargoan, Dhaka, 1207, Bangladesh.

Diana F Gomberg (DF)

Department of Neurology, Boston Children's Hospital, BCH3443, 300 Longwood Ave, Boston, MA, 02115, USA.

Marc G Weisskopf (MG)

Department of Environmental Health, Harvard T.H. Chan School of Public Health, 655 Huntington Avenue, Boston, MA, 02115, USA.

Liming Liang (L)

Department of Biostatistics, Harvard T.H. Chan School of Public Health, 655 Huntington Avenue, Boston, MA, 02115, USA.

Benjamin C Warf (BC)

Department of Neurosurgery, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA, 02115, USA.

David C Christiani (DC)

Department of Environmental Health, Harvard T.H. Chan School of Public Health, 655 Huntington Avenue, Boston, MA, 02115, USA.

Maitreyi Mazumdar (M)

Department of Environmental Health, Harvard T.H. Chan School of Public Health, 655 Huntington Avenue, Boston, MA, 02115, USA. maitreyi.mazumdar@childrens.harvard.edu.
Department of Neurology, Boston Children's Hospital, BCH3443, 300 Longwood Ave, Boston, MA, 02115, USA. maitreyi.mazumdar@childrens.harvard.edu.

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