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Early onset of abnormal glucose tolerance in patients with cystic fibrosis: A systematic review and meta-analysis.
Kéri, Adrienn F; Bajzát, Dorina; Andrásdi, Zita; Juhász, Márk Félix; Nagy, Rita; Kói, Tamás; Kovács, Gábor; Hegyi, Péter; Párniczky, Andrea.
Afiliação
  • Kéri AF; Heim Pál National Pediatric Institute, Budapest, Hungary; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
  • Bajzát D; Heim Pál National Pediatric Institute, Budapest, Hungary; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
  • Andrásdi Z; Heim Pál National Pediatric Institute, Budapest, Hungary.
  • Juhász MF; Heim Pál National Pediatric Institute, Budapest, Hungary; Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
  • Nagy R; Heim Pál National Pediatric Institute, Budapest, Hungary; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary; Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.
  • Kói T; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary; Department of Stochastics, Institute of Mathematics, Budapest University of Technology and Economics, Budapest, Hungary.
  • Kovács G; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Hegyi P; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary; Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary; Institute of Pancreatic Diseases, Semmelweis University, Budapest, Hungary; Translational Pancreatology Research Group, Interdisciplin
  • Párniczky A; Heim Pál National Pediatric Institute, Budapest, Hungary; Centre for Translational Medicine, Semmelweis University, Budapest, Hungary; Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary. Electronic address: andrea.parniczky@gmail.com.
J Cyst Fibros ; 23(4): 616-624, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38458829
ABSTRACT

BACKGROUND:

Despite translational evidences suggesting that cystic fibrosis-related abnormal glucose tolerance (CF-related AGT) may begin early in life and is known to be associated with increased morbidity and mortality, current guidelines recommend screening for AGT only from 10 years of age, thus missing the opportunity for early detection and intervention.

METHODS:

A systematic review and meta-analysis (PROSPERO number CRD42021282516) was conducted on studies that reported data on the prevalence of AGT or its subtypes in CF populations. Pooled proportions, risk, and odds ratios with 95 % confidence intervals (CI) were calculated. One-stage dose-response random-effect meta-analysis was used to assess the effect of age on CF-related diabetes (CFRD).

RESULTS:

The quantitative analysis included 457 studies and data from 520,544 patients. Every third child with CF (chwCF) (0.31 [95 % CI 0.25-0.37]) and every second adult with CF (awCF) (0.51 [95 % CI 0.45-0.57]) were affected by AGT. Even in the 5-10 years of age subgroup, the proportion of AGT was 0.42 [95 % CI 0.34-0.51]. The prevalence of prediabetes remained unchanged (impaired glucose tolerance in chwCF0.14 [95 % CI 0.10-0.18]) vs. awCF0.19 [95 % CI 0.14-0.25]), whereas the proportion of CFRD increased with age (0-5 0.005 [95 % CI 0.0001-0.15]; 5-10 0.05 [95 % CI 0.01-0.27]; 10-18 0.11 [95 % CI 0.08-0.14]; >18 years of age 0.27 [95 % CI 0.24-0.30]).

CONCLUSION:

CF-related AGT is common under 10 years of age. Our study suggests considering earlier AGT screening, starting from 5 years of age. This highlights the imperative for additional research for guideline adjustments and provides the opportunity for early intervention.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Intolerância à Glucose / Fibrose Cística Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Intolerância à Glucose / Fibrose Cística Idioma: En Ano de publicação: 2024 Tipo de documento: Article