Literature DB >> 31974039

Abnormal glucose tolerance and the 50-gram glucose challenge test in Cystic fibrosis.

Saba Sheikh1, A Russell Localio2, Andrea Kelly3, Ronald C Rubenstein4.   

Abstract

Diabetes has emerged as a major co-morbidity in cystic fibrosis (CF). The 75 g oral glucose tolerance test (OGTT) is used to screen for CF-related diabetes (CFRD) but is inconvenient, and adherence to screening is poor. The 50 g glucose challenge test (GCT) is shorter, performed non-fasting, and may serve to pre-screen the subset of individuals requiring confirmatory OGTT. We performed a pilot study in twenty-seven CF individuals across the glucose tolerance spectrum to test whether the GCT could identify subjects with abnormal glucose tolerance defined as 2-h OGTT glucose ≥7.8 mmol/L (2 h-AGT) or 1-h defined as 1-hr OGTT glucose ≥11.1 mmol/L (1 h-AGT). A GCT threshold of 8.1 mmol/L was 73% sensitive and 63% specific for 2hr-AGT and 80% sensitive and 65% specific for 1hr-AGT. Therefore, a screening GCT may reduce need for confirmatory OGTT for identifying AGT but a larger study is warranted to identify a robust cutoff for CFRD.
Copyright © 2020. Published by Elsevier B.V.

Entities:  

Keywords:  Cystic Fibrosis; Cystic Fibrosis Related Diabetes; Glucose challenge test; Oral glucose tolerance test

Year:  2020        PMID: 31974039      PMCID: PMC8293305          DOI: 10.1016/j.jcf.2020.01.003

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  22 in total

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Journal:  Eur J Obstet Gynecol Reprod Biol       Date:  2002-04-10       Impact factor: 2.435

4.  Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: data from the European Epidemiologic Registry of Cystic Fibrosis.

Authors:  C Koch; M Rainisio; U Madessani; H K Harms; M E Hodson; G Mastella; S G McKenzie; J Navarro; B Strandvik
Journal:  Pediatr Pulmonol       Date:  2001-11

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6.  Evaluation of glucose tolerance in cystic fibrosis: comparison of 50-g and 75-g tests.

Authors:  Kathleen M N Lee; Robert J H Miller; Frances M Rosenberg; Stuart H Kreisman
Journal:  J Cyst Fibros       Date:  2006-12-11       Impact factor: 5.482

7.  Influence of the development of diabetes mellitus on clinical status in patients with cystic fibrosis.

Authors:  S Lanng; B Thorsteinsson; J Nerup; C Koch
Journal:  Eur J Pediatr       Date:  1992-09       Impact factor: 3.183

8.  Clinical care guidelines for cystic fibrosis-related diabetes: a position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society.

Authors:  Antoinette Moran; Carol Brunzell; Richard C Cohen; Marcia Katz; Bruce C Marshall; Gary Onady; Karen A Robinson; Kathryn A Sabadosa; Arlene Stecenko; Bonnie Slovis
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9.  Elevation of 1-hour plasma glucose during oral glucose tolerance testing is associated with worse pulmonary function in cystic fibrosis.

Authors:  Jill Brodsky; Shayne Dougherty; Ramkrishna Makani; Ronald C Rubenstein; Andrea Kelly
Journal:  Diabetes Care       Date:  2011-01-12       Impact factor: 19.112

10.  Longitudinal impact of demographic and clinical variables on health-related quality of life in cystic fibrosis.

Authors:  Janice Abbott; Alison M Morton; Margaret A Hurley; Steven P Conway
Journal:  BMJ Open       Date:  2015-05-19       Impact factor: 2.692

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