Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
基本信息
- 批准号:9353817
- 负责人:
- 金额:$ 54.92万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2011
- 资助国家:美国
- 起止时间:2011-06-01 至 2021-08-31
- 项目状态:已结题
- 来源:
- 关键词:12 year oldAdoptedAffectAlbuminsAreaBiological MarkersBloodBrain DiseasesChildChronicClinicalCognitionCommunitiesCommunity Health AidesCongoConsumptionCountryDemocratic Republic of the CongoDeveloping CountriesDevelopmentDiagnosticDietDiseaseDisease OutbreaksEducational InterventionEffectivenessEpidemiologyExposure toFemale of child bearing ageFlourFoodFoundationsGenetic DeterminismGoalsHealthHouseholdHumanHuman ResourcesIncidenceInstitutesInterventionIsoprostanesLipid PeroxidationLipid PeroxidesManihotMeasuresMediatingMentorsMethodologyMethodsMissionModelingMonitorMothersMotorNational Institute of Child Health and Human DevelopmentNational Institute of Diabetes and Digestive and Kidney DiseasesNational Institute of Environmental Health SciencesNational Institute of Mental HealthNational Institute of Neurological Disorders and StrokeNerve DegenerationNeurocognitionNeurodevelopmental DeficitNeurologic DeficitNeuropsychologyOutcomes ResearchOxidantsParaparesisPatternPerformancePostdoctoral FellowPredispositionPreventionPreventive InterventionProcessProteinsProtocols documentationPublic HealthRandomizedResearchResidual stateResourcesRiskRuralSerumSiblingsSourceSpastic ParaparesisSpecialistSpottingsTestingThiocyanatesTimeTrainingUnited States National Institutes of HealthUrineWomanWorkZambiaarmbasechild batterycompare effectivenesscostcost effectivecyanogendisorder preventionevidence basefollow-upglobal healthhomocitrullinemetabolomicsmotor deficitmotor disordernervous system disorderneurotoxicneurotoxicityneurotoxicologynoveloxidationoxidative damagepeerpost interventionpreventprimary outcomeprogramspublic health relevancesecondary outcomeurinarywoman health professional
项目摘要
SUMMARY
Rationale. The proposed project seeks methods to prevent and elucidate biomarkers of neurocognition and
motor deficits associated with chronic dietary reliance on cyanogenic cassava, a staple food crop for more than
600 millions of people living in the tropics. Aim 1 will implement a novel cassava processing method (wetting
method, WTM) that safely removes cyanogenic compounds from cassava flour prior to human consumption in
a stratified village-cluster randomized non-inferiority trial so as to compare the effectiveness of a peer-led
intervention (women training other women in the WTM) with that by community-health worker specialists (2
intervention training arms). We hypothesize that the peer-led WTM intervention is non-inferior to the
specialist-led intervention at the end of the 2-year intervention period and at 1-year follow-up. Task shifting to
peer-led training for WTM should it prove to be effective, would provide for a more cost-effective and
sustainable means to bring this intervention to scale at a community-wide level. Primary outcomes will be the
cassava cyanogenic content produced by the trainee mother (N = 200 in each intervention arm) and urinary
concentrations of thiocyanate (U-SCN) in her konzo and non-konzo sibling children 5 to 12 years of age.
Secondary outcomes will be the neuropsychological performance scores of children assessed using the
Kaufman Assessment Battery for Children (KABC-II) for cognition and the Bruininks/Oseretsky Test (BOT-2)
for motor proficiency. Aim 2 will determine whether post-intervention reductions in cassava cyanogenic content
and child U-SCN are associated with changes in biomarkers of cassava neurotoxicity particularly 8,12-iso-
iPF2α-VI isoprostane (oxidant marker), carbamoylated albumin fragments KVPQVSTPTLVEVSR (residues
438-452) and LDELRDEGKASSAK (residues 206-219), or homocitrulline (carbamoylating markers), and
scores at the KABC-II and BOT-2 testing. We hypothesize that 1) lower cassava cyanogenic content and U-
SCN throughout the two-year intervention period and at one-year follow-up, will be associated with lower
oxidant and carbamoylating markers but higher KABC-II and BOT-2 testing scores; and a similar pattern will be
sustained at 1-year follow-up; and 2) higher levels of oxidation and carbamoylation will be associated with
poorer neuropsychological performance. Biomarkers will be monitored in serum (invasive), dried blood spots
(DBS) (less invasive), or urine (non-invasive) using omic methodologies with the long-term goal of developing
field-based rapid tests to monitor risk for cassava associated neurodevelopmental deficits. Aim 3 will enhance
the research manpower of the konzo-affected Democratic Republic of Congo.
总结
理由。拟议的项目寻求预防和阐明神经认知生物标志物的方法,
运动缺陷与长期饮食依赖生氰木薯有关,生氰木薯是一种主食作物,
六亿人生活在热带地区。目标1将实现一种新的木薯加工方法(润湿
方法,WTM),安全地去除氰化合物从木薯粉之前,人类消费,
分层村群随机非劣效性试验,以比较同行领导的
干预(妇女培训其他妇女参加妇女培训运动)和社区保健工作者专家(2名)的干预
干预训练武器)。我们假设同伴主导的WTM干预不劣于
在2年干预期结束时和1年随访时进行专家主导的干预。任务转移到
同行领导的WTM培训如果证明是有效的,将提供更具成本效益的,
可持续意味着在全社区一级推广这一干预措施。主要成果将是
由受训母亲产生的木薯生氰含量(每个干预组N = 200)和尿
在她的konzo和非konzo同胞子女5至12岁的硫氰酸盐(U-SCN)浓度。
次要结果将是儿童的神经心理学表现评分,
考夫曼儿童认知成套评估(KABC-II)和Bruininks/Oseretsky测验(BOT-2)
运动能力的测试目标2将确定干预后木薯生氰含量的减少
和儿童U-SCN与木薯神经毒性生物标志物的变化有关,特别是8,12-异
iPF 2 α-VI异前列烷(氧化剂标记物)、氨甲酰化白蛋白片段KVPQVSTPTLVEVSR(残基
438-452)和LDELRDEGKASSAK(残基206-219),或高瓜氨酸(氨甲酰化标记),和
在KABC-II和BOT-2测试中得分。我们假设:1)较低的木薯生氰含量和U-
在整个两年干预期和一年随访时,SCN与较低的
氧化剂和氨甲酰化标记物,但KABC-II和BOT-2测试得分较高;
在1年随访时持续; 2)较高水平的氧化和氨甲酰化将与
神经心理学表现较差。将在血清(侵入性)、干血斑中监测生物标志物
(DBS)(微创)或尿液(非侵入性)使用组学方法,长期目标是开发
实地快速测试,以监测木薯相关神经发育缺陷的风险。目标3将提高
刚果民主共和国的研究人员。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Daniel Desire Tshala-Katumbay其他文献
Daniel Desire Tshala-Katumbay的其他文献
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{{ truncateString('Daniel Desire Tshala-Katumbay', 18)}}的其他基金
Onchocerciasis-associated Neurodevelopmental Deficits: The Hit Squad
盘尾丝虫病相关的神经发育缺陷:杀手小队
- 批准号:
8842499 - 财政年份:2014
- 资助金额:
$ 54.92万 - 项目类别:
Onchocerciasis-associated Neurodevelopmental Deficits: The Hit Squad
盘尾丝虫病相关的神经发育缺陷:杀手小队
- 批准号:
8619310 - 财政年份:2014
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
8073616 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
8429486 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
9145383 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
8538012 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
8813957 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
8274545 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
9223972 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
Toxicodietary and genetic determinants of susceptibility to neurodegeneration
神经退行性疾病易感性的毒性饮食和遗传决定因素
- 批准号:
8628123 - 财政年份:2011
- 资助金额:
$ 54.92万 - 项目类别:
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