Nicole J Jensen, Ane J Porse, Helena Z Wodschow, Helene Speyer, Jesper Krogh, Lisbeth Marner, Michael Gejl, Albert Gjedde, Jørgen Rungby
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Criteria were studies assessing brain glucose metabolism (uptake or metabolic rate) by 18F-2-fluoro-2-deoxy-D-glucose-positron emission tomography in individuals characterized by measures of or clinical proxies for insulin resistance (eg, type 2 diabetes and obesity).</p><p><strong>Data extraction: </strong>Two independent investigators extracted data and assessed study quality.</p><p><strong>Data synthesis: </strong>We applied random-effects models to pool Hedge's g standardized mean differences. Insulin resistance was associated with decreased brain glucose metabolism during fasting [-0.47 SD, 95% confidence interval (CI): -0.73 to -0.22, P < .001, I2 = 71%] and increased metabolism during insulin stimulation (1.44 SD, 95% CI 0.79 to 2.09, P = .002, I2 = 43%). Contrary to type 2 diabetes and other insulin resistance-related conditions, obesity was not associated with brain hypometabolism in fasting states (0.29 SD, 95% CI -.81 to 1.39).</p><p><strong>Conclusion: </strong>Metabolic conditions modify associations between insulin resistance and brain glucose metabolism; ie, most individuals with insulin resistance display hypometabolism during fasting and hypermetabolism during insulin stimulation.</p>","PeriodicalId":50238,"journal":{"name":"Journal of Clinical Endocrinology & Metabolism","volume":" ","pages":"e525-e537"},"PeriodicalIF":5.0000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11747694/pdf/","citationCount":"0","resultStr":"{\"title\":\"Relation of Insulin Resistance to Brain Glucose Metabolism in Fasting and Hyperinsulinemic States: A Systematic Review and Meta-analysis.\",\"authors\":\"Nicole J Jensen, Ane J Porse, Helena Z Wodschow, Helene Speyer, Jesper Krogh, Lisbeth Marner, Michael Gejl, Albert Gjedde, Jørgen Rungby\",\"doi\":\"10.1210/clinem/dgae570\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Context: </strong>Abnormal brain glucose metabolism may cause cognitive disease in type 2 diabetes, yet the relation between insulin resistance and brain glucose metabolism has not been systematically described.</p><p><strong>Objective: </strong>We evaluated the impact of metabolic condition (fasting vs insulin stimulation, eg, from hyperinsulinemic clamp) on the association between insulin resistance of different etiologies and brain glucose metabolism.</p><p><strong>Data sources: </strong>PubMed, Embase, Cochrane Library, and Web of Science were systematically searched from inception until February 2022.</p><p><strong>Study selection: </strong>Of 656 unique records, we deemed 31 eligible. 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引用次数: 0
摘要
背景:异常的脑糖代谢可能导致2型糖尿病患者的认知疾病,但胰岛素抵抗与脑糖代谢之间的关系尚未得到系统描述:我们评估了代谢条件(空腹与胰岛素刺激,如高胰岛素血症钳夹)对不同病因引起的胰岛素抵抗与脑糖代谢之间关系的影响:对 PubMed、Embase、Cochrane Library 和 Web of Science 进行了系统检索:在 656 条唯一记录中,我们认为有 31 条符合条件。标准是通过18F-2-氟-2-脱氧-D-葡萄糖正电子发射断层扫描([18F]-FDG-PET)评估以胰岛素抵抗或临床代用品(如2型糖尿病和肥胖)为特征的个体的脑葡萄糖代谢(摄取量或代谢率)的研究:两名独立研究人员提取数据并评估研究质量:我们采用随机效应模型对Hedge's g标准化均值差异进行了汇总。胰岛素抵抗与空腹时脑糖代谢下降有关(-0.47SD,95%CI:-0.73 至 -0.22,p结论:代谢条件会改变胰岛素抵抗与脑糖代谢之间的关系:代谢条件会改变胰岛素抵抗与脑葡萄糖代谢之间的关联,即大多数胰岛素抵抗患者在空腹时会表现出低代谢,而在胰岛素刺激时会表现出高代谢。
Relation of Insulin Resistance to Brain Glucose Metabolism in Fasting and Hyperinsulinemic States: A Systematic Review and Meta-analysis.
Context: Abnormal brain glucose metabolism may cause cognitive disease in type 2 diabetes, yet the relation between insulin resistance and brain glucose metabolism has not been systematically described.
Objective: We evaluated the impact of metabolic condition (fasting vs insulin stimulation, eg, from hyperinsulinemic clamp) on the association between insulin resistance of different etiologies and brain glucose metabolism.
Data sources: PubMed, Embase, Cochrane Library, and Web of Science were systematically searched from inception until February 2022.
Study selection: Of 656 unique records, we deemed 31 eligible. Criteria were studies assessing brain glucose metabolism (uptake or metabolic rate) by 18F-2-fluoro-2-deoxy-D-glucose-positron emission tomography in individuals characterized by measures of or clinical proxies for insulin resistance (eg, type 2 diabetes and obesity).
Data extraction: Two independent investigators extracted data and assessed study quality.
Data synthesis: We applied random-effects models to pool Hedge's g standardized mean differences. Insulin resistance was associated with decreased brain glucose metabolism during fasting [-0.47 SD, 95% confidence interval (CI): -0.73 to -0.22, P < .001, I2 = 71%] and increased metabolism during insulin stimulation (1.44 SD, 95% CI 0.79 to 2.09, P = .002, I2 = 43%). Contrary to type 2 diabetes and other insulin resistance-related conditions, obesity was not associated with brain hypometabolism in fasting states (0.29 SD, 95% CI -.81 to 1.39).
Conclusion: Metabolic conditions modify associations between insulin resistance and brain glucose metabolism; ie, most individuals with insulin resistance display hypometabolism during fasting and hypermetabolism during insulin stimulation.
期刊介绍:
The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.