GLUCOSE AND INSULIN ABNORMALITIES IN FANCONI ANEMIA
GLUCOSE AND INSULIN ABNORMALITIES IN FANCONI ANEMIA
批准号:
7606005
负责人:
Anna Petryk
金额:
$0.3万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-12-01 至 2007-11-30
关键词:
Androgen TherapyAndrogensChildComputer Retrieval of Information on Scientific Projects DatabaseDiabetes MellitusFanconi&aposs AnemiaFundingGenomicsGlucoseGlucose tolerance testGrantInstitutionInsulinInsulin ResistanceKnowledgeLifeMutationNon-Insulin-Dependent Diabetes MellitusOGTTParentsPatientsPediatricsPrevalenceProteinsRelative (related person)ReportingResearchResearch PersonnelResistanceResourcesRiskSamplingScienceSiblingsSourceStressThinkingUnited States National Institutes of Healthbasehuman FANCG proteininsulin secretiontrend
中文摘要
点击翻译按钮获取中文摘要
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Previous studies have demonstrated an association between Fanconi anemia (FA) and diabetes mellitus (DM). Swift et al (Science 1972) reported an increased prevalence of diabetes in relatives of children with FA. More recently, Wajnrajch et al (Pediatrics 2001) reported abnormalities in oral glucose tolerance testing (OGTT) in 25% of patients with FA with 72% of patients manifesting resistance to insulin action; however, the patients were not stratified based on pre- or post-BMT or androgen therapy. Androgens, BMT and stress can be associated with abnormalities in OGTT. The authors also correlated these abnormalities with complementation group and found a trend toward insulin resistance in the complementation group FA-G. However, it is the mutation for FA-C that lies in the region encoding a protein thought to be associated with type 2 DM, not FA-G (Rothschild et al, Genomics 1995). Therefore, we plan to further define the insulin and glucose abnormalities in FA through insulin-modified frequently sampled iv glucose tolerance test (FSIGT) in addition to OGTT to provide pathophysiologic information about insulin secretion and sensitivity. We will also be able to determine the contribution of androgens and complementation groups to the insulin and glucose abnormalities. These results will enable us to better predict the FA patients who will develop diabetes. This knowledge has become important now that many more children with FA are living into adulthood. If an association with a complentation group is found, we could then hypothesize that the heterozygous parents and possibly siblings would be at increased risk for DM as well.
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依托单位:
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依托单位:
海外基金