Serum Uric Acid as a Biomarker of Cognitive and Functional Decline in Late Life
Serum Uric Acid as a Biomarker of Cognitive and Functional Decline in Late Life
批准号:
7706235
负责人:
Tracy Dawn Vannorsdall
金额:
$7.22万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-08-31
关键词:
AdultAgeAgingAlcohol abuseAttentionAuthorization documentationBiological MarkersBloodBrainCardiovascular systemCerebral IschemiaCerebrumClinical TrialsCognitionCognitiveCommunitiesDataData AnalysesDevelopmentElderlyElderly womanGoalsGrantHealthHypertensionImpaired cognitionIndividual DifferencesInjuryInvestigationMeasuresMediatingNormal RangeObservational StudyParticipantPerformancePharmaceutical PreparationsPhysical ExaminationPilot ProjectsProductionPropertyProspective StudiesRaceRiskSamplingSerumSmokingTestingUric AcidWomen&aposs Healthbasediabetes educationfunctional declineinterestpreventpublic health relevancesex
中文摘要
DESCRIPTION (provided by applicant): Uric acid is rapidly gaining attention because of its seemingly contradictory properties in relation to brain function. In our prior cross-sectional, observational studies of community-dwelling adults, we have demonstrated that mildly elevated-- but still normal-- levels of serum uric acid are associated with significantly poorer cognitive performance and with greater cerebral ischemic burden, even after controlling for age, sex, race, education, diabetes, hypertension, smoking, and alcohol abuse. We have also demonstrated that individual differences in cerebral ischemia mediate the association between uric acid and mild cognitive dysfunction. Taken together, our results support the notion that even mild elevations of serum uric acid are associated with structural and functional brain changes, specifically involving the development of ischemic injury. These findings are interesting and suggest that a clinical trial may be warranted to determine whether uric acid lowering medications prevent or reverse mild cognitive dysfunction in elderly adults with high normal serum uric acid. However, the sample on which these findings were based was relatively small and the relationships were strictly cross-sectional. Therefore, the goal of this pilot project is to replicate these findings in a larger cross-sectional sample and extend our findings by determining whether high normal concentrations of serum uric acid are associated with mild cognitive dysfunction and adaptive functioning longitudinally. We are also seeking to determine whether any observed associations between uric and adaptive functioning are mediated by declines in cognition. To achieve these goals, we have applied for and been granted permission to analyze data from the Women's Health and Aging Study II (WHAS II), a prospective study of healthy elderly women. Participants of the WHAS II underwent serial physical examinations, blood draws (including serum uric acid), cognitive testing, and assessments of adaptive functioning. Should the findings from this investigation indicate that high normal serum uric acid increases the risk of mild cognitive dysfunction longitudinally, after controlling for other health, cardiovascular, and demographic variables it, this would provide powerful evidence further justifying the need for a clinical trial aimed at reducing serum uric acid production in elderly adults with mildly elevated uric acid. PUBLIC HEALTH RELEVANCE: The goal of this pilot project is to replicate and expand on our previous cross-sectional findings relating elevations in serum uric acid to mild cognitive dysfunction in elderly adults by examining both cross-sectional and longitudinal data from the Women's Health and Aging Study-II (WHAS-II). Should the findings from this investigation indicate that high normal serum uric acid increases the risk of mild cognitive dysfunction longitudinally, this would provide powerful evidence further justifying the need for a clinical trial aimed at reducing serum uric acid production in elderly adults with mildly elevated uric acid.
英文摘要
DESCRIPTION (provided by applicant): Uric acid is rapidly gaining attention because of its seemingly contradictory properties in relation to brain function. In our prior cross-sectional, observational studies of community-dwelling adults, we have demonstrated that mildly elevated-- but still normal-- levels of serum uric acid are associated with significantly poorer cognitive performance and with greater cerebral ischemic burden, even after controlling for age, sex, race, education, diabetes, hypertension, smoking, and alcohol abuse. We have also demonstrated that individual differences in cerebral ischemia mediate the association between uric acid and mild cognitive dysfunction. Taken together, our results support the notion that even mild elevations of serum uric acid are associated with structural and functional brain changes, specifically involving the development of ischemic injury. These findings are interesting and suggest that a clinical trial may be warranted to determine whether uric acid lowering medications prevent or reverse mild cognitive dysfunction in elderly adults with high normal serum uric acid. However, the sample on which these findings were based was relatively small and the relationships were strictly cross-sectional. Therefore, the goal of this pilot project is to replicate these findings in a larger cross-sectional sample and extend our findings by determining whether high normal concentrations of serum uric acid are associated with mild cognitive dysfunction and adaptive functioning longitudinally. We are also seeking to determine whether any observed associations between uric and adaptive functioning are mediated by declines in cognition. To achieve these goals, we have applied for and been granted permission to analyze data from the Women's Health and Aging Study II (WHAS II), a prospective study of healthy elderly women. Participants of the WHAS II underwent serial physical examinations, blood draws (including serum uric acid), cognitive testing, and assessments of adaptive functioning. Should the findings from this investigation indicate that high normal serum uric acid increases the risk of mild cognitive dysfunction longitudinally, after controlling for other health, cardiovascular, and demographic variables it, this would provide powerful evidence further justifying the need for a clinical trial aimed at reducing serum uric acid production in elderly adults with mildly elevated uric acid. PUBLIC HEALTH RELEVANCE: The goal of this pilot project is to replicate and expand on our previous cross-sectional findings relating elevations in serum uric acid to mild cognitive dysfunction in elderly adults by examining both cross-sectional and longitudinal data from the Women's Health and Aging Study-II (WHAS-II). Should the findings from this investigation indicate that high normal serum uric acid increases the risk of mild cognitive dysfunction longitudinally, this would provide powerful evidence further justifying the need for a clinical trial aimed at reducing serum uric acid production in elderly adults with mildly elevated uric acid.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Automated Presurgical Language Mapping via Deep Learning for Multimodal Brain Connectivity
-
批准号:10415207
-
项目类别:
-
资助金额:$18.09万
-
财政年份:2021
-
负责人:Tracy Dawn Vannorsdall
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: