共 50 条
Screening strategies for glucose tolerance abnormalities and diabetes in people with cystic fibrosis
被引:7
|作者:
Weiss, Laurence
[1
]
Reix, Philippe
[2
]
Mosnier-Pudar, Helen
[3
]
Ronsin, Olivia
[4
]
Beltrand, Jacques
[5
,6
]
Reynaud, Quitterie
[7
,8
]
Mely, Laurent
[9
]
Burgel, Pierre-Regis
[10
,11
,12
]
Stremler, Nathalie
[13
]
Rakotoarisoa, Luc
[14
]
Galderisi, Alfonso
[5
,6
]
Perge, Kevin
[2
]
Bendelac, Nathalie
[2
]
Abely, Michel
[15
]
Kessler, Laurence
[14
,16
]
机构:
[1] Hop Univ Strasbourg, Paediat Cyst Fibrosis Resources & Competences Ctr, Strasbourg, France
[2] Hosp Civils Lyon, Paediat Cyst Fibrosis Resources & Competences Ctr, Paediat Pulmonol & Allergol Dept, Lyon, France
[3] Hop Cochin, Assistance Publ Hop Paris, Dept Endocrinol, Paris, France
[4] CHU Marseille, Hop Nord, Dept Endocrinol Diabet & Nutr, Adult Cyst Fibrosis Resources & Competences Ctr, Marseille, France
[5] Univ Paris Cite, Paediat Endocrinol Gynaecol & Diabetol, Hop Necker Enfants Malad, APHP Ctr, Paris, France
[6] Inst Cochin, INSERM, U1016, Paris, France
[7] Hosp Civils Lyon, Adult Cyst Fibrosis Resources & Competences Ctr, Dept Med, Lyon, France
[8] Univ Claude Bernard Lyon 1, RESHAPE, INSERM, U1290, F-69008 Lyon, France
[9] Hosp Civils Lyon, Mixed Cyst Fibrosis Resources & Competences Ctr, Hop Rene Sabran, Giens, France
[10] Hop Cochin, Assistance Publ Hop Paris, Natl Reference Ctr Cyst Fibrosis, Paris, France
[11] Hop Cochin, Assistance Publ Hop Paris, Pneumol Dept, Paris, France
[12] Univ Paris Cite, Inst Cochin, INSERM, U1016, Paris, France
[13] CHU Marseille, Paediat Cyst Fibrosis Resources & Competences Ctr, Hop Timone, Marseille, France
[14] Hop Univ Strasbourg, Adult Cyst Fibrosis Resources & Competences Ctr, Endocrinol Diabet & Nutr Dept, Strasbourg, France
[15] Hop Americain, Mixed Cyst Fibrosis Resources & Competences Ctr, Reims, France
[16] Univ Strasbourg, INSERM, UMR 1260, Regenerat Nanomed, Strasbourg, France
关键词:
Continuous glucose monitoring;
Cystic fibrosis-related diabetes;
Screening;
INSULIN-SECRETION;
YOUNG-CHILDREN;
LUNG-FUNCTION;
MICROVASCULAR COMPLICATIONS;
GLYCATED HEMOGLOBIN;
PREVALENCE;
GROWTH;
TOOL;
TRANSPLANTATION;
EPIDEMIOLOGY;
D O I:
10.1016/j.diabet.2023.101444
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The increase in life expectancy of patients with cystic fibrosis has come with new comorbidities, particularly diabetes. The gradual development of glucose tolerance abnormalities means that 30 to 40% of adults will be diabetic. Cystic fibrosis-related diabetes is a major challenge in the care of these patients because it is a mor-bidity and mortality factor at all stages of the disease. Early glucose tolerance abnormalities observed from childhood, before the stage of diabetes, are also associated with a poor pulmonary and nutritional outcome. The long asymptomatic period justifies systematic screening with an annual oral glucose tolerance test from the age of 10 years. However, this strategy does not take into account the new clinical profiles of patients with cystic fibrosis, recent pathophysiological knowledge of glucose tolerance abnormalities, and the emer-gence of new diagnostic tools in diabetology. In this paper, we summarise the challenges of screening in the current context of new patient profiles - patients who are pregnant, have transplants, or are being treated with fibrosis conductance transmembrane regulator modulators - and put forward an inventory of the vari-ous screening methods for cystic fibrosis-related diabetes, including their applications, limitations and prac-tical implications.(c) 2023 Elsevier Masson SAS. All rights reserved.
引用
收藏
页数:12
相关论文