Daniel Gottlieb , Layla A. Abushamat , Kristen J. Nadeau , Judith G. Regensteiner , Jane E.B. Reusch , Kalie L. Tommerdahl , John Rice , Leslie A. Knaub , Cynthia M.F. Monaco , Thomas J. Hawke , Christopher G.R. Perry , Melanie G. Cree , Irene E. Schauer
{"title":"Muscle mitochondrial function is impaired in adults with type 1 diabetes","authors":"Daniel Gottlieb , Layla A. Abushamat , Kristen J. Nadeau , Judith G. Regensteiner , Jane E.B. Reusch , Kalie L. Tommerdahl , John Rice , Leslie A. Knaub , Cynthia M.F. Monaco , Thomas J. Hawke , Christopher G.R. Perry , Melanie G. Cree , Irene E. Schauer","doi":"10.1016/j.jdiacomp.2024.108798","DOIUrl":null,"url":null,"abstract":"<div><h3>Aims</h3><p>Type 1 diabetes has been associated with mitochondrial dysfunction. However, the mechanism of this dysfunction in adults remains unclear.</p></div><div><h3>Methods</h3><p>A secondary analysis was conducted using data from several clinical trials measuring <em>in-vivo</em> and <em>ex-vivo</em> mitochondrial function in adults with type 1 diabetes (<em>n</em> = 34, age 38.8 ± 14.6 years) and similarly aged controls (<em>n</em> = 59, age 44.6 ± 13.9 years). <em>In-vivo</em> mitochondrial function was assessed before, during, and after isometric exercise with <sup>31</sup>phosphorous magnetic resonance spectroscopy. High resolution respirometry of vastus lateralis muscle tissue was used to assess <em>ex-vivo</em> measures.</p></div><div><h3>Results</h3><p><em>In-vivo</em> data showed higher rates of anaerobic glycolysis (<em>p</em> = 0.013), and a lower maximal mitochondrial oxidative capacity (<em>p</em> = 0.012) and mitochondrial efficiency (<em>p</em> = 0.024) in adults with type 1 diabetes. After adjustment for age and percent body fat maximal mitochondrial capacity (<em>p</em> = 0.014) continued to be lower and anaerobic glycolysis higher (<em>p</em> = 0.040) in adults with type 1 diabetes. <em>Ex-vivo</em> data did not demonstrate significant differences between the two groups.</p></div><div><h3>Conclusions</h3><p>The <em>in-vivo</em> analysis demonstrates that adults with type 1 diabetes have mitochondrial dysfunction. This builds on previous research showing <em>in-vivo</em> mitochondrial dysfunction in youths with type 1 diabetes and suggests that defects in substrate or oxygen delivery may play a role in <em>in-vivo</em> dysfunction.</p></div>","PeriodicalId":15659,"journal":{"name":"Journal of diabetes and its complications","volume":"38 8","pages":"Article 108798"},"PeriodicalIF":2.9000,"publicationDate":"2024-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of diabetes and its complications","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1056872724001247","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Aims
Type 1 diabetes has been associated with mitochondrial dysfunction. However, the mechanism of this dysfunction in adults remains unclear.
Methods
A secondary analysis was conducted using data from several clinical trials measuring in-vivo and ex-vivo mitochondrial function in adults with type 1 diabetes (n = 34, age 38.8 ± 14.6 years) and similarly aged controls (n = 59, age 44.6 ± 13.9 years). In-vivo mitochondrial function was assessed before, during, and after isometric exercise with 31phosphorous magnetic resonance spectroscopy. High resolution respirometry of vastus lateralis muscle tissue was used to assess ex-vivo measures.
Results
In-vivo data showed higher rates of anaerobic glycolysis (p = 0.013), and a lower maximal mitochondrial oxidative capacity (p = 0.012) and mitochondrial efficiency (p = 0.024) in adults with type 1 diabetes. After adjustment for age and percent body fat maximal mitochondrial capacity (p = 0.014) continued to be lower and anaerobic glycolysis higher (p = 0.040) in adults with type 1 diabetes. Ex-vivo data did not demonstrate significant differences between the two groups.
Conclusions
The in-vivo analysis demonstrates that adults with type 1 diabetes have mitochondrial dysfunction. This builds on previous research showing in-vivo mitochondrial dysfunction in youths with type 1 diabetes and suggests that defects in substrate or oxygen delivery may play a role in in-vivo dysfunction.
期刊介绍:
Journal of Diabetes and Its Complications (JDC) is a journal for health care practitioners and researchers, that publishes original research about the pathogenesis, diagnosis and management of diabetes mellitus and its complications. JDC also publishes articles on physiological and molecular aspects of glucose homeostasis.
The primary purpose of JDC is to act as a source of information usable by diabetes practitioners and researchers to increase their knowledge about mechanisms of diabetes and complications development, and promote better management of people with diabetes who are at risk for those complications.
Manuscripts submitted to JDC can report any aspect of basic, translational or clinical research as well as epidemiology. Topics can range broadly from early prediabetes to late-stage complicated diabetes. Topics relevant to basic/translational reports include pancreatic islet dysfunction and insulin resistance, altered adipose tissue function in diabetes, altered neuronal control of glucose homeostasis and mechanisms of drug action. Topics relevant to diabetic complications include diabetic retinopathy, neuropathy and nephropathy; peripheral vascular disease and coronary heart disease; gastrointestinal disorders, renal failure and impotence; and hypertension and hyperlipidemia.