Associations Between Glucose Tolerance, Insulin Secretion, Muscle and Fat Mass in Cystic Fibrosis.

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM Clinical Medicine Insights-Endocrinology and Diabetes Pub Date : 2021-08-13 eCollection Date: 2021-01-01 DOI:10.1177/11795514211038259
Bibi Uhre Nielsen, Daniel Faurholt-Jepsen, Peter Sandor Oturai, Tavs Qvist, Rikke Krogh-Madsen, Terese Lea Katzenstein, James Shaw, Christian Ritz, Tacjana Pressler, Thomas Peter Almdal, Inger Hee Mabuza Mathiesen
{"title":"Associations Between Glucose Tolerance, Insulin Secretion, Muscle and Fat Mass in Cystic Fibrosis.","authors":"Bibi Uhre Nielsen,&nbsp;Daniel Faurholt-Jepsen,&nbsp;Peter Sandor Oturai,&nbsp;Tavs Qvist,&nbsp;Rikke Krogh-Madsen,&nbsp;Terese Lea Katzenstein,&nbsp;James Shaw,&nbsp;Christian Ritz,&nbsp;Tacjana Pressler,&nbsp;Thomas Peter Almdal,&nbsp;Inger Hee Mabuza Mathiesen","doi":"10.1177/11795514211038259","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>A frequent comorbidity in cystic fibrosis (CF) is CF related diabetes (CFRD) caused by a gradual decline in insulin secretion. The reduction in the anabolic hormone, insulin, might explain the weight loss that precedes onset of CFRD. We investigated the association between muscle and fat mass in relation to glucose tolerance and insulin function.</p><p><strong>Methods: </strong>In a cross-sectional study with CF patients (⩾18 years), we conducted an oral glucose tolerance test and dual energy X-ray absorptiometry scan (DXA). Based on plasma glucose, glucose tolerance was defined as normal (NGT): 1-hour <11.1 mmol/L and 2-hour <7.8 mmol/L, impaired (IGT): 2-hour ⩾7.8 and <11.1 mmol/L or CFRD: 2-hour ⩾11.1 mmol/L. Insulin resistance (HOMA-IR) was derived from fasting levels of plasma glucose and plasma insulin, and fat-free and fat mass index (kg/m<sup>2</sup>) from DXA. Associations were evaluated using linear regression models adjusted for age, sex, and pancreas insufficiency.</p><p><strong>Results: </strong>Among 79 CF patients with exocrine pancreas insufficiency, impairment of glucose tolerance corresponded to reduced insulin secretion. In the IGT group the fat-free mass index (FFMI) was 1.2 kg/m<sup>2</sup> (95% CI: [-2.3, -0.03] kg/m<sup>2</sup>, <i>P</i> = .044) lower compared to the NGT group. FFMI increased insignificantly by 0.4 kg/m<sup>2</sup> (95% CI: [-0.6, 1.5] kg/m<sup>2</sup>, <i>P</i> = .422) among the insulin-treated CFRD group compared to IGT. Fat mass index (FMI) was not different between groups but tended to decrease with glucose tolerance impairment. For each 100 pmol/L increase in fasting insulin FFMI increased by 1.77 kg/m<sup>2</sup> (95% CI: [0.21, 3.33] kg/m<sup>2</sup>/pmol/L/100) and FMI increased by 6.15 kg/m<sup>2</sup> (95% CI: [3.87, 8.44] kg/m<sup>2</sup>/pmol/L/100). In multivariate analyses, HOMA-IR was positively associated with FFMI (β = 0.5 kg/m<sup>2</sup>/HOMA-IR, 95% CI: [0.08, 0.92] kg/m<sup>2</sup>/HOMA-IR, <i>P</i> = .021) and FMI (β = 1.5 kg/m<sup>2</sup>/HOMA-IR, 95% CI: [0.87, 2.15] kg/m<sup>2</sup>/HOMA-IR, <i>P</i> < .001).</p><p><strong>Conclusions: </strong>Muscle mass was significantly lower among participants with impaired glucose tolerance (IGT), while muscle mass was normalized among those treated with insulin.</p>","PeriodicalId":44715,"journal":{"name":"Clinical Medicine Insights-Endocrinology and Diabetes","volume":"14 ","pages":"11795514211038259"},"PeriodicalIF":2.7000,"publicationDate":"2021-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c0/4f/10.1177_11795514211038259.PMC8369959.pdf","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Medicine Insights-Endocrinology and Diabetes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/11795514211038259","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 4

Abstract

Background: A frequent comorbidity in cystic fibrosis (CF) is CF related diabetes (CFRD) caused by a gradual decline in insulin secretion. The reduction in the anabolic hormone, insulin, might explain the weight loss that precedes onset of CFRD. We investigated the association between muscle and fat mass in relation to glucose tolerance and insulin function.

Methods: In a cross-sectional study with CF patients (⩾18 years), we conducted an oral glucose tolerance test and dual energy X-ray absorptiometry scan (DXA). Based on plasma glucose, glucose tolerance was defined as normal (NGT): 1-hour <11.1 mmol/L and 2-hour <7.8 mmol/L, impaired (IGT): 2-hour ⩾7.8 and <11.1 mmol/L or CFRD: 2-hour ⩾11.1 mmol/L. Insulin resistance (HOMA-IR) was derived from fasting levels of plasma glucose and plasma insulin, and fat-free and fat mass index (kg/m2) from DXA. Associations were evaluated using linear regression models adjusted for age, sex, and pancreas insufficiency.

Results: Among 79 CF patients with exocrine pancreas insufficiency, impairment of glucose tolerance corresponded to reduced insulin secretion. In the IGT group the fat-free mass index (FFMI) was 1.2 kg/m2 (95% CI: [-2.3, -0.03] kg/m2, P = .044) lower compared to the NGT group. FFMI increased insignificantly by 0.4 kg/m2 (95% CI: [-0.6, 1.5] kg/m2, P = .422) among the insulin-treated CFRD group compared to IGT. Fat mass index (FMI) was not different between groups but tended to decrease with glucose tolerance impairment. For each 100 pmol/L increase in fasting insulin FFMI increased by 1.77 kg/m2 (95% CI: [0.21, 3.33] kg/m2/pmol/L/100) and FMI increased by 6.15 kg/m2 (95% CI: [3.87, 8.44] kg/m2/pmol/L/100). In multivariate analyses, HOMA-IR was positively associated with FFMI (β = 0.5 kg/m2/HOMA-IR, 95% CI: [0.08, 0.92] kg/m2/HOMA-IR, P = .021) and FMI (β = 1.5 kg/m2/HOMA-IR, 95% CI: [0.87, 2.15] kg/m2/HOMA-IR, P < .001).

Conclusions: Muscle mass was significantly lower among participants with impaired glucose tolerance (IGT), while muscle mass was normalized among those treated with insulin.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
囊性纤维化中葡萄糖耐量、胰岛素分泌、肌肉和脂肪量的关系
背景:囊性纤维化(CF)的常见合并症是由胰岛素分泌逐渐下降引起的CF相关性糖尿病(CFRD)。合成代谢激素胰岛素的减少可能解释了CFRD发病前的体重减轻。我们研究了肌肉和脂肪量与葡萄糖耐量和胰岛素功能之间的关系。方法:在与CF患者(大于或等于18年)的横断面研究中,我们进行了口服葡萄糖耐量试验和双能x射线吸收测量扫描(DXA)。根据血浆葡萄糖,葡萄糖耐量定义为正常(NGT):从DXA开始1小时2)。使用线性回归模型对年龄、性别和胰腺功能不全进行校正。结果:79例伴有外分泌胰腺功能不全的CF患者中,糖耐量损害与胰岛素分泌减少相对应。IGT组的无脂质量指数(FFMI)比NGT组低1.2 kg/m2 (95% CI: [-2.3, -0.03] kg/m2, P = 0.044)。与IGT相比,胰岛素治疗的CFRD组FFMI增加了0.4 kg/m2 (95% CI: [-0.6, 1.5] kg/m2, P = .422)。脂肪质量指数(FMI)在两组间无显著差异,但随着糖耐量的降低有降低的趋势。空腹胰岛素每增加100 pmol/L, FFMI增加1.77 kg/m2 (95% CI: [0.21, 3.33] kg/m2/pmol/L/100), FMI增加6.15 kg/m2 (95% CI: [3.87, 8.44] kg/m2/pmol/L/100)。在多变量分析中,HOMA-IR与FFMI (β = 0.5 kg/m2/HOMA-IR, 95% CI: [0.08, 0.92] kg/m2/HOMA-IR, P = 0.021)和FMI (β = 1.5 kg/m2/HOMA-IR, 95% CI: [0.87, 2.15] kg/m2/HOMA-IR, P)呈正相关。结论:糖耐量受损(IGT)参与者的肌肉质量显著降低,而胰岛素治疗组的肌肉质量正常化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.30
自引率
0.00%
发文量
15
审稿时长
8 weeks
期刊最新文献
Assessing the Effects of HbA1c Reduction on Alleviating Chronic Nonspecific Low Back Pain in Prediabetic Non-obese Patients: A Non-Randomized Controlled Trial. Trends of Pathological Findings in Patients with Thyroid Diseases: A Single-center, Retrospective Study. Rethinking the Terminology: A Perspective on Renaming Polycystic Ovary Syndrome for an Enhanced Pathophysiological Understanding. Inhibitory Effect of TCF7L2 on Pancreatic β-Cell Dedifferentiation via ERK/MAPK Signaling Pathway in Diabetes. Exploring the Impact of Social Media on Attaining HbA1c Targets in Individuals with Type 2 Diabetes Mellitus in Iraq: A Cross-Sectional Study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1