Endocr Pract. 2019 Mar;25(3):254-262. doi: 10.4158/EP-2018-0461.
Cystic fibrosis-related diabetes (CFRD) is associated with adverse clinical outcomes and should be screened for by an annual oral glucose tolerance test (OGTT). Since pathophysiologic studies have mainly been performed in a pediatric/adolescent, nontransplanted collective, we aimed to assess parameters of insulin secretion and sensitivity in adult cystic fibrosis (CF) patients after lung transplantation (LT).
Twelve adult CF patients after LT without known diabetes (33.3 ± 11.5 years; body mass index [BMI] 21.5 ± 3.3 kg/m) and 8 control subjects matched by age (36.0 ± 6.6 years; P>.05), BMI (22.3 ± 1.5 kg/m; P>.05), and gender (CON group) underwent a 3-hour OGTT with glucose, insulin, and C-peptide measurements. Parameters of insulin secretion and sensitivity as well as lipid profiles were assessed.
In the CF group, 4 patients were diagnosed with overt diabetes (CFRD) compared to CF patients without diabetes (CF-noDM), of whom 6 had indeterminate glycemia with 1-h glucose values >200 mg/dL. The insulin peak after glucose load occurred after 30 minutes in CON, after 90 minutes in CF-noDM, and was missing in CFRD. Insulin sensitivity was comparable between the groups. Beta-cell glucose sensitivity was markedly reduced in CFRD (10.7 ± 5.8 pmol/minmmM), higher in CF-noDM (39.9 ± 23.4 pmol/minmmM), but still significantly lower compared to CON (108.3 ± 53.9 pmol/minmmM; P = .0008). CFRD patients exhibited increased triglyceride levels and decreased high-density lipoprotein levels.
Adult CF patients after LT have profound disturbances in glucose metabolism, with a high rate of undetected diabetes and markedly delayed insulin secretion. Curbed beta-cell glucose sensitivity rather than insulin resistance explains postprandial hyperglycemia and is accompanied by abnormalities in lipid metabolism.
AUC = area under the curve; BMI = body mass index; CF = cystic fibrosis; CFRD = cystic fibrosis-related diabetes; CFTR = cystic fibrosis transmembrane-conductance regulator; CF-TX = cystic fibrosis patients who underwent lung transplantation; CGM = continuous glucose monitoring; HbA1c = glycated hemoglobin; HDL = high-density lipoprotein; INDET = indeterminate glycemia; LDL = low-density lipoprotein; LT = lung transplantation; OGIS = oral glucose sensitivity index; OGTT = oral glucose tolerance test; QUICKI = quantitative insulin sensitivity check index.
囊性纤维化相关糖尿病(CFRD)与不良临床结局相关,应通过每年的口服葡萄糖耐量试验(OGTT)进行筛查。由于病理生理学研究主要在儿科/青少年、未移植的人群中进行,我们旨在评估肺移植(LT)后成年囊性纤维化(CF)患者的胰岛素分泌和敏感性参数。
12 名成年 CF 患者在 LT 后无已知糖尿病(33.3 ± 11.5 岁;体重指数 [BMI] 21.5 ± 3.3 kg/m)和 8 名年龄匹配的对照组(36.0 ± 6.6 岁;P>.05)、BMI(22.3 ± 1.5 kg/m;P>.05)和性别(CON 组)接受 3 小时 OGTT,检测葡萄糖、胰岛素和 C 肽。评估胰岛素分泌和敏感性参数以及血脂谱。
在 CF 组中,与 CF 无糖尿病患者(CF-noDM)相比,4 名患者被诊断为显性糖尿病(CFRD),其中 6 名患者 1 小时血糖值>200mg/dL,存在不确定的血糖。在 CON 中,葡萄糖负荷后的胰岛素峰值出现在 30 分钟后,在 CF-noDM 中出现在 90 分钟后,而在 CFRD 中则缺失。两组的胰岛素敏感性相当。CFRD 患者的胰岛β细胞葡萄糖敏感性明显降低(10.7 ± 5.8 pmol/minmmM),CF-noDM 患者的胰岛β细胞葡萄糖敏感性升高(39.9 ± 23.4 pmol/minmmM),但仍明显低于 CON(108.3 ± 53.9 pmol/minmmM;P =.0008)。CFRD 患者表现出血甘油三酯水平升高和高密度脂蛋白水平降低。
LT 后的成年 CF 患者存在严重的葡萄糖代谢紊乱,糖尿病的漏诊率很高,胰岛素分泌明显延迟。餐后高血糖的原因是胰岛β细胞葡萄糖敏感性受损,而不是胰岛素抵抗,同时伴有脂代谢异常。