• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

囊性纤维化中葡萄糖不耐受的机制。

Mechanisms of glucose intolerance in cystic fibrosis.

机构信息

The Adult Cystic Fibrosis Unit, The Cardiothoracic Centre NHS Trust, Liverpool L143PE, UK.

出版信息

Diabet Med. 2009 Jun;26(6):582-8. doi: 10.1111/j.1464-5491.2009.02738.x.

DOI:10.1111/j.1464-5491.2009.02738.x
PMID:19538232
Abstract

AIMS

Although cystic fibrosis-related diabetes (CFRD), a poor prognostic factor in cystic fibrosis (CF), is characterized by insulinopenia, the role of insulin resistance is unclear. Using a prospective study design, we measured insulin resistance, pancreatic beta-cell function and correlated glycaemic status with clinical parameters.

METHODS

Oral glucose tolerance test was performed in 60 stable adult CF patients. Insulin sensitivity and beta-cell function were measured using the homeostatic model assessment (HOMA2), Stumvoll and oral glucose insulin sensitivity (OGIS) indices.

RESULTS

Forty-two (70%) had normal glucose tolerance (NGT), 10 (17%) impaired glucose tolerance (IGT) and eight (13%) CFRD. There was no difference in insulin sensitivity among the three groups (HOMA2: NGT 280, IGT 250, CFRD 339, P = 0.42; Stumvoll: NGT 0.128, IGT 0.126, CFRD 0.129, P = 0.76; and OGIS: NGT 515, IGT 472, CFRD 472, P = 0.12). Pancreatic beta-cell function (CFRD 50% vs. NGT 67%; P < 0.05) and first-phase insulin secretion were reduced in CFRD (250 vs. NGT 509; P = 0.004). First-phase insulin secretion was inversely correlated with 1-h (r = -0.74; P < 0.0001) and 2-h glucose levels (r = -0.34; P < 0.05). There was no difference in body mass index or poor lung function (forced expiratory volume in 1 s: CFRD 54% vs. NGT 65%; P = 0.43). However, there were more hospital admissions in the CFRD group (three vs. NGT one per patient per year; P < 0.05).

CONCLUSIONS

CFRD is characterized by qualitative and quantitative defects in insulin secretion, but not insulin resistance, and is associated with increased hospital admissions for pulmonary exacerbations.

摘要

目的

虽然囊性纤维化相关糖尿病(CFRD)是囊性纤维化(CF)的一个预后不良因素,但它以胰岛素缺乏为特征,而胰岛素抵抗的作用尚不清楚。我们采用前瞻性研究设计,测量了胰岛素抵抗、胰岛β细胞功能,并将血糖状态与临床参数相关联。

方法

对 60 例稳定的成年 CF 患者进行口服葡萄糖耐量试验。使用稳态模型评估(HOMA2)、Stumvoll 和口服葡萄糖胰岛素敏感性(OGIS)指数来测量胰岛素敏感性和胰岛β细胞功能。

结果

42 例(70%)患者糖耐量正常(NGT),10 例(17%)患者糖耐量受损(IGT),8 例(13%)患者患有 CFRD。三组之间的胰岛素敏感性无差异(HOMA2:NGT 280,IGT 250,CFRD 339,P=0.42;Stumvoll:NGT 0.128,IGT 0.126,CFRD 0.129,P=0.76;OGIS:NGT 515,IGT 472,CFRD 472,P=0.12)。CFRD 患者的胰岛β细胞功能(CFRD 50% vs. NGT 67%;P<0.05)和第一时相胰岛素分泌减少(250 vs. NGT 509;P=0.004)。第一时相胰岛素分泌与 1 小时(r=-0.74;P<0.0001)和 2 小时血糖水平呈负相关(r=-0.34;P<0.05)。体重指数或肺功能不良无差异(用力呼气量 1 秒:CFRD 54% vs. NGT 65%;P=0.43)。然而,CFRD 组的住院次数更多(每例患者每年 CFRD 组 3 次,NGT 组 1 次;P<0.05)。

结论

CFRD 的特征是胰岛素分泌的质和量的缺陷,但不存在胰岛素抵抗,与因肺部恶化而住院的次数增加有关。

相似文献

1
Mechanisms of glucose intolerance in cystic fibrosis.囊性纤维化中葡萄糖不耐受的机制。
Diabet Med. 2009 Jun;26(6):582-8. doi: 10.1111/j.1464-5491.2009.02738.x.
2
Glucose intolerance in cystic fibrosis as a determinant of pulmonary function and clinical status.囊性纤维化患者葡萄糖耐量异常作为肺功能和临床状况的决定因素。
Diabetes Res Clin Pract. 2015 Dec;110(3):276-84. doi: 10.1016/j.diabres.2015.10.007. Epub 2015 Oct 14.
3
Insulin-secretion abnormalities and clinical deterioration related to impaired glucose tolerance in cystic fibrosis.囊性纤维化中与糖耐量受损相关的胰岛素分泌异常及临床恶化
Eur J Endocrinol. 2005 Feb;152(2):241-7. doi: 10.1530/eje.1.01836.
4
Insulin sensitivity, disposition index and insulin clearance in cystic fibrosis: a cross-sectional study.囊性纤维化患者的胰岛素敏感性、处置指数和胰岛素清除率:一项横断面研究。
Diabetologia. 2024 Oct;67(10):2188-2198. doi: 10.1007/s00125-024-06220-6. Epub 2024 Aug 2.
5
Natural history of glucose intolerance in patients with cystic fibrosis: ten-year prospective observation program.囊性纤维化患者葡萄糖不耐受的自然史:十年前瞻性观察计划。
J Pediatr. 2010 Apr;156(4):613-7. doi: 10.1016/j.jpeds.2009.10.019. Epub 2009 Dec 3.
6
β-Cell secretory defects are present in pancreatic insufficient cystic fibrosis with 1-hour oral glucose tolerance test glucose ≥155 mg/dL.β 细胞分泌缺陷存在于胰腺功能不全型囊性纤维化中,1 小时口服葡萄糖耐量试验血糖≥155mg/dL。
Pediatr Diabetes. 2018 Nov;19(7):1173-1182. doi: 10.1111/pedi.12700. Epub 2018 Jun 21.
7
Glucose Tolerance Stages in Cystic Fibrosis Are Identified by a Unique Pattern of Defects of Beta-Cell Function.囊性纤维化的葡萄糖耐量阶段是通过β细胞功能缺陷的独特模式来识别的。
J Clin Endocrinol Metab. 2021 Mar 25;106(4):e1793-e1802. doi: 10.1210/clinem/dgaa932.
8
Cystic fibrosis-related diabetes: the role of peripheral insulin resistance and beta-cell dysfunction.囊性纤维化相关糖尿病:外周胰岛素抵抗和β细胞功能障碍的作用。
Diabet Med. 2002 Mar;19(3):221-6. doi: 10.1046/j.1464-5491.2002.00666.x.
9
The relationship between insulin secretion, the insulin-like growth factor axis and growth in children with cystic fibrosis.囊性纤维化患儿胰岛素分泌、胰岛素样生长因子轴与生长之间的关系。
Clin Endocrinol (Oxf). 2002 Mar;56(3):383-9. doi: 10.1046/j.1365-2265.2002.01484.x.
10
Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance.处置指数可识别出糖耐量正常的囊性纤维化患者β细胞功能缺陷。
J Cyst Fibros. 2015 Jan;14(1):135-41. doi: 10.1016/j.jcf.2014.06.004. Epub 2014 Jul 4.

引用本文的文献

1
Utility of Continuous Glucose Monitors for Improved Detection of Cystic Fibrosis-Related Diabetes.连续血糖监测仪在改善囊性纤维化相关糖尿病检测方面的效用。
Pediatr Pulmonol. 2025 Aug;60(8):e71267. doi: 10.1002/ppul.71267.
2
Effects of Elevated Glucose on Bacterial Respiratory Infections in Cystic Fibrosis and Chronic Airway Diseases.高血糖对囊性纤维化和慢性气道疾病中细菌呼吸道感染的影响。
Int J Mol Sci. 2025 Jun 11;26(12):5597. doi: 10.3390/ijms26125597.
3
Cystic fibrosis-related diabetes is associated with reduced islet protein expression of GLP-1 receptor and perturbation of cell-specific transcriptional programs.
囊性纤维化相关性糖尿病与 GLP-1 受体的胰岛蛋白表达减少和细胞特异性转录程序紊乱有关。
Sci Rep. 2024 Oct 28;14(1):25689. doi: 10.1038/s41598-024-76722-1.
4
Pancreas and islet morphology in cystic fibrosis: clues to the etiology of cystic fibrosis-related diabetes.囊性纤维化中的胰腺和胰岛形态:囊性纤维化相关糖尿病病因的线索。
Front Endocrinol (Lausanne). 2023 Nov 23;14:1269139. doi: 10.3389/fendo.2023.1269139. eCollection 2023.
5
Clinical Observations in Patients With Cystic Fibrosis-Related Diabetes and Self-Reported Ototoxicity Symptoms.囊性纤维化相关糖尿病患者及自我报告耳毒性症状患者的临床观察
Am J Audiol. 2023 Nov 28;33(1):1-9. doi: 10.1044/2023_AJA-22-00237.
6
The long-term effects of insulin use in incident cystic fibrosis-related diabetes: a target trial emulated using longitudinal national registry data.胰岛素用于新发囊性纤维化相关糖尿病的长期影响:一项利用纵向国家登记数据模拟的目标试验。
ERJ Open Res. 2022 Nov 7;8(4). doi: 10.1183/23120541.00170-2022. eCollection 2022 Oct.
7
Impact of CFTR Modulators on Beta-Cell Function in Children and Young Adults with Cystic Fibrosis.CFTR调节剂对患有囊性纤维化的儿童和青年β细胞功能的影响。
J Clin Med. 2022 Jul 17;11(14):4149. doi: 10.3390/jcm11144149.
8
Cystic Fibrosis-Related Diabetes (CFRD): Overview of Associated Genetic Factors.囊性纤维化相关糖尿病(CFRD):相关遗传因素概述
Diagnostics (Basel). 2021 Mar 22;11(3):572. doi: 10.3390/diagnostics11030572.
9
CFTR Deficiency Affects Glucose Homeostasis via Regulating GLUT4 Plasma Membrane Transportation.囊性纤维化跨膜传导调节因子缺乏通过调控葡萄糖转运蛋白4的质膜转运影响葡萄糖稳态。
Front Cell Dev Biol. 2021 Feb 15;9:630654. doi: 10.3389/fcell.2021.630654. eCollection 2021.
10
Survival in a bad neighborhood: pancreatic islets in cystic fibrosis.在恶劣环境中生存:囊性纤维化中的胰岛
J Endocrinol. 2019 Feb 1. doi: 10.1530/JOE-18-0468.