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Prenatal Arsenic Exposure, Folic Acid Use and Spina Bifida in Bangladesh
Prenatal Arsenic Exposure, Folic Acid Use and Spina Bifida in Bangladesh
Prenatal Arsenic Exposure, Folic Acid Use and Spina Bifida in Bangladesh

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211151426
ISBN  
9798382783840
DDC  
613
저자명  
Wei, Chih-Fu.
서명/저자  
Prenatal Arsenic Exposure, Folic Acid Use and Spina Bifida in Bangladesh
발행사항  
[Sl] : Harvard University, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
122 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
주기사항  
Advisor: Mazumdar, Maitryei.
학위논문주기  
Thesis (Ph.D.)--Harvard University, 2024.
초록/해제  
요약Spina bifida, a severe neural tube defect, constitutes a substantial population health burden globally. It increases the risk of stillbirth, infant and child mortality, and multiple neurological conditions, including lower limb paralysis and urinary and fecal incontinence. The etiology of spina bifida is multifactorial, and the prevalence varies greatly across different populations. Prenatal folic acid supplementation is an effective strategy for prevention of spina bifida; folic acid corrects folate deficiency and supports multiple essential reactions during neural tube development. However, folic acid alone does not lead to complete prevention of spina bifida, and the interactions of folic acid and naturally occurring folate with genetic and environmental factors are not fully understood.Arsenic exposure is a risk factor for spina bifida, and arsenic toxicity is closely linked to folate metabolism. Animal studies have shown that arsenic exposure increases the risk of neural tube defects by influencing folate metabolism and reducing available methyl groups. The risk of neural tube defects was particularly high in animals with folate deficiencies and those with genetic mutations related to folate metabolism. Epidemiologic studies also showed varying risks of spina bifida by arsenic exposure and mothers' folic acid use. The association between arsenic exposure and spina bifida and its interactions with folic acid is particularly important for the population in Bangladesh. The country experiences widespread groundwater arsenic pollution, prevalent folate deficiency, and a higher prevalence of spina bifida and other neural tube defects. Therefore, this dissertation aims to understand the interactions between prenatal arsenic exposure, folic acid, and genetic factors on spina bifida risk in Bangladesh.Overview of DissertationThe first two studies utilized data from a case-control study at the National Institute of Neurosciences & Hospital, Dhaka, Bangladesh. The first study examined the associations between mothers' arsenic exposure and spina bifida risk. This study showed evidence of effect modification-the association between mothers' folic acid use and spina bifida risk differed by mothers' toenail arsenic concentrations. Folic acid use reduced the risk of spina bifida among mothers with lower arsenic exposure, but this association was not observed among mothers with higher arsenic exposure. The second study explored the potential interactions between mothers' toenail arsenic concentrations and polymorphisms in both mothers' and infants' arsenic and folate metabolism genes. In this paper, we found that infants' AS3MT, MTR, and mothers' CBS and DNMT1 variants interacted with mothers' arsenic exposure to alter the risk of spina bifida. In the third study, we reviewed existing literature to estimate spina bifida prevalence in Bangladesh. Additionally, we assessed the prevention of neural tube defects under different folic acid provisions and arsenic reduction strategies in a hypothetical cohort with high arsenic exposure in Bangladesh. This study quantified the reduction in the prevalence and number of cases with neural tube defects when combining folic acid provision and arsenic reduction strategies.These studies expand the current understanding of the interaction between arsenic and folic acid, which influences the risk of spina bifida in Bangladesh. The dissertation advocates the approach of integrating environmental health interventions and nutritional strategies to optimize the prevention of spina bifida and neural tube defects. Specifically, the dissertation highlights the importance of addressing environmental arsenic exposure to enhance spina bifida prevention, especially in Bangladesh, where arsenic exposure remains prevalent.
일반주제명  
Environmental health
일반주제명  
Health sciences
일반주제명  
Epidemiology
일반주제명  
Genetics
키워드  
Spina bifida
키워드  
Lower limb paralysis
키워드  
Folate metabolism
키워드  
Arsenic toxicity
기타저자  
Harvard University Population Health Sciences
기본자료저록  
Dissertations Abstracts International. 85-12B.
전자적 위치 및 접속  
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MARC

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■1001  ▼aWei,  Chih-Fu.▼0(orcid)0000-0002-9711-6231
■24510▼aPrenatal  Arsenic  Exposure,  Folic  Acid  Use  and  Spina  Bifida  in  Bangladesh
■260    ▼a[Sl]▼bHarvard  University▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a122  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-12,  Section:  B.
■500    ▼aAdvisor:  Mazumdar,  Maitryei.
■5021  ▼aThesis  (Ph.D.)--Harvard  University,  2024.
■520    ▼aSpina  bifida,  a  severe  neural  tube  defect,  constitutes  a  substantial  population  health  burden  globally.  It  increases  the  risk  of  stillbirth,  infant  and  child  mortality,  and  multiple  neurological  conditions,  including  lower  limb  paralysis  and  urinary  and  fecal  incontinence.  The  etiology  of  spina  bifida  is  multifactorial,  and  the  prevalence  varies  greatly  across  different  populations.  Prenatal  folic  acid  supplementation  is  an  effective  strategy  for  prevention  of  spina  bifida;  folic  acid  corrects  folate  deficiency  and  supports  multiple  essential  reactions  during  neural  tube  development.  However,  folic  acid  alone  does  not  lead  to  complete  prevention  of  spina  bifida,  and  the  interactions  of  folic  acid  and  naturally  occurring  folate  with  genetic  and  environmental  factors  are  not  fully  understood.Arsenic  exposure  is  a  risk  factor  for  spina  bifida,  and  arsenic  toxicity  is  closely  linked  to  folate  metabolism.  Animal  studies  have  shown  that  arsenic  exposure  increases  the  risk  of  neural  tube  defects  by  influencing  folate  metabolism  and  reducing  available  methyl  groups.  The  risk  of  neural  tube  defects  was  particularly  high  in  animals  with  folate  deficiencies  and  those  with  genetic  mutations  related  to  folate  metabolism.  Epidemiologic  studies  also  showed  varying  risks  of  spina  bifida  by  arsenic  exposure  and  mothers'  folic  acid  use.  The  association  between  arsenic  exposure  and  spina  bifida  and  its  interactions  with  folic  acid  is  particularly  important  for  the  population  in  Bangladesh.  The  country  experiences  widespread  groundwater  arsenic  pollution,  prevalent  folate  deficiency,  and  a  higher  prevalence  of  spina  bifida  and  other  neural  tube  defects.  Therefore,  this  dissertation  aims  to  understand  the  interactions  between  prenatal  arsenic  exposure,  folic  acid,  and  genetic  factors  on  spina  bifida  risk  in  Bangladesh.Overview  of  DissertationThe  first  two  studies  utilized  data  from  a  case-control  study  at  the  National  Institute  of  Neurosciences  &  Hospital,  Dhaka,  Bangladesh.  The  first  study  examined  the  associations  between  mothers'  arsenic  exposure  and  spina  bifida  risk.  This  study  showed  evidence  of  effect  modification-the  association  between  mothers'  folic  acid  use  and  spina  bifida  risk  differed  by  mothers'  toenail  arsenic  concentrations.  Folic  acid  use  reduced  the  risk  of  spina  bifida  among  mothers  with  lower  arsenic  exposure,  but  this  association  was  not  observed  among  mothers  with  higher  arsenic  exposure.  The  second  study  explored  the  potential  interactions  between  mothers'  toenail  arsenic  concentrations  and  polymorphisms  in  both  mothers'  and  infants'  arsenic  and  folate  metabolism  genes.  In  this  paper,  we  found  that  infants'  AS3MT,  MTR,  and  mothers'  CBS  and  DNMT1  variants  interacted  with  mothers'  arsenic  exposure  to  alter  the  risk  of  spina  bifida.  In  the  third  study,  we  reviewed  existing  literature  to  estimate  spina  bifida  prevalence  in  Bangladesh.  Additionally,  we  assessed  the  prevention  of  neural  tube  defects  under  different  folic  acid  provisions  and  arsenic  reduction  strategies  in  a  hypothetical  cohort  with  high  arsenic  exposure  in  Bangladesh.  This  study  quantified  the  reduction  in  the  prevalence  and  number  of  cases  with  neural  tube  defects  when  combining  folic  acid  provision  and  arsenic  reduction  strategies.These  studies  expand  the  current  understanding  of  the  interaction  between  arsenic  and  folic  acid,  which  influences  the  risk  of  spina  bifida  in  Bangladesh.  The  dissertation  advocates  the  approach  of  integrating  environmental  health  interventions  and  nutritional  strategies  to  optimize  the  prevention  of  spina  bifida  and  neural  tube  defects.  Specifically,  the  dissertation  highlights  the  importance  of  addressing  environmental  arsenic  exposure  to  enhance  spina  bifida  prevention,  especially  in  Bangladesh,  where  arsenic  exposure  remains  prevalent.
■590    ▼aSchool  code:  0084.
■650  4▼aEnvironmental  health
■650  4▼aHealth  sciences
■650  4▼aEpidemiology
■650  4▼aGenetics
■653    ▼aSpina  bifida
■653    ▼aLower  limb  paralysis
■653    ▼aFolate  metabolism
■653    ▼aArsenic  toxicity
■690    ▼a0470
■690    ▼a0566
■690    ▼a0369
■690    ▼a0766
■71020▼aHarvard  University▼bPopulation  Health  Sciences.
■7730  ▼tDissertations  Abstracts  International▼g85-12B.
■790    ▼a0084
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17161652▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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