Literature DB >> 33331877

Glucose tolerance stages in Cystic Fibrosis are idenfied by a unique pattern of defects of Beta-cell function.

Claudia Piona1, Sonia Volpi2, Chiara Zusi1, Enza Mozzillo3, Antonella Tosco4, Adriana Franzese3, Valeria Raia4, Maria Linda Boselli5, Maddalena Trombetta5, Marco Cipolli2, Riccardo C Bonadonna6,7, Claudio Maffeis1.   

Abstract

AIM: To assess the order of severity of the defects of three direct determinants of glucose regulation, i.e., beta-cell function, insulin clearance and insulin sensitivity, in patients with CF categorized according their glucose tolerance status, including early elevation of mid-OGTT glucose values (>140 and < 200 mg/dL), named AGT140.
METHODS: Two hundred and thirty-two CF patients aged 10-25 underwent OGTT. Beta-cell function and insulin clearance were estimated by OGTT mathematical modelling and OGTT-derived biomarkers of insulin secretion and sensitivity were calculated. The association between five glucose tolerance stages [NGT, AGT140, Indeterminate glucose Tolerance (INDET), impaired glucose tolerance (IGT), Cystic fibrosis related diabetes (CFRD)] and glucometabolic variables was assessed with general linear model.
RESULTS: Beta-cell function and insulin sensitivity progressively worsened across glucose tolerance stages (p<0.001) with AGT140 patients significantly differing from NGT (all p<0.01). AGT140 and INDET showed a degree of beta-cell dysfunction similar to IGT and CFRD, respectively (all p<0.01). Insulin clearance was not significantly associated with glucose tolerance stages (p=0.162). Each class of glucose tolerance was uniquely identified by a specific combination of defects of the direct determinants of glucose regulation.
CONCLUSIONS: In CF patients each of the five glucose tolerance stages shows a unique pattern of defects of the direct determinants of glucose regulation, with AGT140 patients significantly differing from NGT and being similar to IGT. These findings suggest to recognize AGT 140 as a distinct glucose tolerance class and to reconsider the grade of glucometabolic deterioration across glucose tolerance stages in CF.
© The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Cystic Fibrosis; Glucose Metabolism; Insulin sensitivity; Oral glucose tolerance test; β-cell function

Year:  2020        PMID: 33331877     DOI: 10.1210/clinem/dgaa932

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  6 in total

1.  Diabetes and Prediabetes in Children With Cystic Fibrosis: A Systematic Review of the Literature and Recommendations of the Italian Society for Pediatric Endocrinology and Diabetes (ISPED).

Authors:  Enza Mozzillo; Roberto Franceschi; Claudia Piona; Stefano Passanisi; Alberto Casertano; Dorina Pjetraj; Giulio Maltoni; Valeria Calcaterra; Vittoria Cauvin; Valentino Cherubini; Giuseppe D'Annunzio; Adriana Franzese; Anna Paola Frongia; Fortunato Lombardo; Donatella Lo Presti; Maria Cristina Matteoli; Elvira Piccinno; Barbara Predieri; Ivana Rabbone; Andrea Enzo Scaramuzza; Sonia Toni; Stefano Zucchini; Claudio Maffeis; Riccardo Schiaffini
Journal:  Front Endocrinol (Lausanne)       Date:  2021-04-29       Impact factor: 5.555

2.  Characterization of glucose metabolism in youth with vs. without cystic fibrosis liver disease: A pilot study.

Authors:  Maria Socorro Rayas; Kara S Hughan; Rida Javaid; Andrea Kelly; Marzieh Salehi
Journal:  J Clin Transl Endocrinol       Date:  2022-03-21

3.  Oral Glucose Tolerance Test in Patients with Cystic Fibrosis Compared to the Overweight and Obese: A Different Approach in Understanding the Results.

Authors:  Mirela Mogoi; Liviu Laurentiu Pop; Mihaela Dediu; Ioana Mihaiela Ciuca
Journal:  Children (Basel)       Date:  2022-04-08

4.  Impact of CFTR Modulators on Beta-Cell Function in Children and Young Adults with Cystic Fibrosis.

Authors:  Claudia Piona; Enza Mozzillo; Antonella Tosco; Sonia Volpi; Francesco Maria Rosanio; Chiara Cimbalo; Adriana Franzese; Valeria Raia; Chiara Zusi; Federica Emiliani; Maria Linda Boselli; Maddalena Trombetta; Riccardo Crocina Bonadonna; Marco Cipolli; Claudio Maffeis
Journal:  J Clin Med       Date:  2022-07-17       Impact factor: 4.964

5.  Increased sputum lactate during oral glucose tolerance test in cystic fibrosis.

Authors:  Peter Østrup Jensen; Bibi Uhre Nielsen; Mette Kolpen; Tacjana Pressler; Daniel Faurholt-Jepsen; Inger Hee Mabuza Mathiesen
Journal:  APMIS       Date:  2022-05-30       Impact factor: 3.428

Review 6.  Comparison of continuous glucose monitoring to reference standard oral glucose tolerance test for the detection of dysglycemia in cystic Fibrosis: A systematic review.

Authors:  Shanal Kumar; Michael Pallin; Georgia Soldatos; Helena Teede
Journal:  J Clin Transl Endocrinol       Date:  2022-09-27
  6 in total

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