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峰值口服葡萄糖耐量试验血糖与小儿囊性纤维化患者肺功能降低相关。

Peak OGTT glucose is associated with lower lung function in young children with cystic fibrosis.

机构信息

Department of Respiratory Medicine, Sydney Children's Hospital, Randwick, NSW, Australia; School of Women's and Children's Health, Medicine, The University of New South Wales, Randwick, NSW, Australia; Molecular and Integrative Cystic Fibrosis Research Centre (miCF_RC), Sydney, Australia.

School of Women's and Children's Health, Medicine, The University of New South Wales, Randwick, NSW, Australia.

出版信息

J Cyst Fibros. 2020 Mar;19(2):305-309. doi: 10.1016/j.jcf.2019.05.005. Epub 2019 May 22.


DOI:10.1016/j.jcf.2019.05.005
PMID:31126898
Abstract

BACKGROUND: Screening for Cystic Fibrosis-related diabetes is recommended in patients with CF <10 years old when there are concerns about growth and lung function. The Oral Glucose Tolerance Test (OGTT) is recommended but has not been validated in this cohort. We sought to determine whether the 2-h OGTT, the gold standard diagnostic test for CFRD, detects clinical decline in children with CF <10 years old. METHODS: We analysed blood glucose(BG) levels collected every 30 min during OGTT in 27 children with CF < 10 years old, comparing the 2-hour BG (BG), peak BG (BG) and Area Under the Curve(AUC) for glucose and the association with lung function and nutritional status. We also compared the OGTT results with results from Continuous Glucose Monitoring (CGM) performed in 11 participants. RESULTS: The BG was higher than the BG in 25/27 (93%) participants. There was a significant inverse correlation between BG and weight z-score (r = -0.56, p = .002) and between BG and FEV (r = -0.54, p = .014) that was not present for BG. A significant inverse correlation was also identified between fasting insulin level and elevated glucose on CGM, defined as AUC >7.8 mmol/L (r - 0.69, p = .027) or as % time > 7.8 (r = - 0.76, p = .011). CONCLUSIONS: Children with CF < 10 years of age with higher BG on OGTT have lower lung function and weight z- scores that may not be identified using the 2 h OGTT BG. CGM also identifies glucose excursions in young children with CF.

摘要

背景:当 CF 患者有生长和肺功能方面的担忧时,建议对 <10 岁的 CF 患者进行囊性纤维化相关糖尿病(Cystic Fibrosis-related diabetes,CFRD)筛查。推荐使用口服葡萄糖耐量试验(Oral Glucose Tolerance Test,OGTT),但尚未在该队列中得到验证。我们旨在确定 2 小时 OGTT 是否可检测出 <10 岁 CF 患儿的临床衰退。

方法:我们分析了 27 名 <10 岁 CF 患儿 OGTT 过程中每 30 分钟采集的血糖(Blood Glucose,BG)水平,比较了 2 小时 BG(BG)、峰值 BG(BG)和血糖曲线下面积(Area Under the Curve,AUC)与肺功能和营养状况的相关性。我们还将 OGTT 结果与 11 名参与者的连续血糖监测(Continuous Glucose Monitoring,CGM)结果进行了比较。

结果:27 名参与者中有 25 名(93%)的 BG 高于 BG。BG 与体重 z 评分呈显著负相关(r = -0.56,p = 0.002),与 FEV 呈显著负相关(r = -0.54,p = 0.014),但 BG 与 FEV 无相关性。空腹胰岛素水平与 CGM 上的高血糖(定义为 AUC >7.8mmol/L,r = -0.69,p = 0.027;或 %时间>7.8,r = -0.76,p = 0.011)之间也存在显著的负相关。

结论:在 OGTT 中 BG 较高的 <10 岁 CF 患儿,其肺功能和体重 z 评分较低,而这些可能无法通过 2 小时 OGTT BG 检测出来。CGM 还可识别 CF 幼儿的血糖波动。

相似文献

[1]
Peak OGTT glucose is associated with lower lung function in young children with cystic fibrosis.

J Cyst Fibros. 2020-3

[2]
Glucose >200 mg/dL during Continuous Glucose Monitoring Identifies Adult Patients at Risk for Development of Cystic Fibrosis Related Diabetes.

J Diabetes Res. 2016

[3]
Oral glucose tolerance test and continuous glucose monitoring to assess diabetes development in cystic fibrosis patients.

Endocrinol Diabetes Nutr (Engl Ed). 2018-1

[4]
Early assessment of glucose abnormalities during continuous glucose monitoring associated with lung function impairment in cystic fibrosis patients.

J Cyst Fibros. 2014-7

[5]
Abnormal glucose tolerance and lung function in children with cystic fibrosis. Comparing oral glucose tolerance test and continuous glucose monitoring.

J Cyst Fibros. 2021-9

[6]
Continuous glucose monitoring and advanced glycation endproducts for prediction of clinical outcomes and development of cystic fibrosis-related diabetes in adults with CF.

Front Endocrinol (Lausanne). 2024

[7]
[Value of continuous glucose monitoring in screening for diabetes in cystic fibrosis].

Arch Pediatr. 2009-12

[8]
Sensitivity and specificity of different methods for cystic fibrosis-related diabetes screening: is the oral glucose tolerance test still the standard?

J Pediatr Endocrinol Metab. 2017-1-1

[9]
The Relationship Between Continuous Glucose Monitoring and OGTT in Youth and Young Adults With Cystic Fibrosis.

J Clin Endocrinol Metab. 2022-1-18

[10]
Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females.

Pediatr Diabetes. 2016-11-22

引用本文的文献

[1]
20 years of the Montreal Cystic Fibrosis Related Diabetes Screening Cohort: key insights.

Eur Respir Rev. 2025-5-14

[2]
Evaluation of Oral Glucose Tolerance Test Results in Children with Cystic Fibrosis.

Sisli Etfal Hastan Tip Bul. 2024-9-30

[3]
Maternal Glycemia During Pregnancy and Child Lung Function: A Prospective Cohort Study.

Diabetes Care. 2024-11-1

[4]
Advances in diabetes technology to improve the lives of people with cystic fibrosis.

Diabetologia. 2024-10

[5]
The Role of Continuous Glucose Monitoring in Detecting Early Dysglycemia and Clinical Outcomes in Patients with Cystic Fibrosis.

Medicina (Kaunas). 2024-3-14

[6]
Continuous glucose monitoring and advanced glycation endproducts for prediction of clinical outcomes and development of cystic fibrosis-related diabetes in adults with CF.

Front Endocrinol (Lausanne). 2024

[7]
2. Diagnosis and Classification of Diabetes: Standards of Care in Diabetes-2024.

Diabetes Care. 2024-1-1

[8]
ISPAD Clinical Practice Consensus Guidelines 2022: Management of cystic fibrosis-related diabetes in children and adolescents.

Pediatr Diabetes. 2022-12

[9]
2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes-2023.

Diabetes Care. 2023-1-1

[10]
Clinical practice versus guidelines for the screening of cystic fibrosis-related diabetes: A French survey from the 47 centers.

J Clin Transl Endocrinol. 2022-4-4

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