Literature DB >> 29580828

Continuous glucose monitoring abnormalities in cystic fibrosis youth correlate with pulmonary function decline.

Christine L Chan1, Timothy Vigers2, Laura Pyle3, Philip S Zeitler2, Scott D Sagel4, Kristen J Nadeau2.   

Abstract

BACKGROUND: To characterize glucose patterns with continuous glucose monitoring (CGM) in cystic fibrosis (CF) and assess relationships between CGM and clinical outcomes.
METHODS: 110 CF youth and healthy controls (HC), 10-18 years, wore CGM up to 7 days. Correlations between CGM and lung function and BMI z-score change over the prior year were determined.
RESULTS: Multiple CGM measures were higher in CF Normal Glycemic (CFNG) youth versus HC (peak glucose, excursions >140 mg/dl/day, %time > 140 mg/dl, standard deviation (SD) and mean amplitude of glycemic excursions (MAGE)). Hypoglycemia was no different among groups. In CF, decline in FEV1% and FVC% correlated with maximum CGM glucose, excursions >200 mg/dl/day, SD, and MAGE.
CONCLUSIONS: CFNG youth have higher glucoses and glucose variability than HC on CGM. Higher and more variable glucoses correlate with lung function decline. Whether earlier treatment of CGM abnormalities improves lung function in CF requires further study.
Copyright © 2018 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Continuous glucose monitoring; Cystic fibrosis related diabetes; Pediatrics

Mesh:

Substances:

Year:  2018        PMID: 29580828      PMCID: PMC6151303          DOI: 10.1016/j.jcf.2018.03.008

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


  44 in total

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2.  Impaired fasting glucose in cystic fibrosis.

Authors:  Brigitte I Frohnert; Katie Larson Ode; Antoinette Moran; Brandon M Nathan; Theresa Laguna; Bonnie Holme; William Thomas
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3.  Nadirs of oral glucose tolerance tests are independent of age and sex.

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4.  Effect of hyperglycaemia on glucose concentration of human nasal secretions.

Authors:  David M Wood; Amanda L Brennan; Barbara J Philips; Emma H Baker
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5.  Conventional measures underestimate glycaemia in cystic fibrosis patients.

Authors:  L Dobson; C D Sheldon; A T Hattersley
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6.  Long-term effect of insulin treatment in cystic fibrosis-related diabetes.

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Review 8.  New insights into cystic fibrosis-related diabetes in children.

Authors:  Katie L Ode; Antoinette Moran
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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
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10.  Prognostic relevance of hypoglycemia following an oral glucose challenge for cystic fibrosis-related diabetes.

Authors:  Kerstin Radike; Katharina Molz; Reinhard W Holl; Britta Poeter; Helge Hebestreit; Manfred Ballmann
Journal:  Diabetes Care       Date:  2011-04       Impact factor: 19.112

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  13 in total

1.  Hemoglobin A1c Accurately Predicts Continuous Glucose Monitoring-Derived Average Glucose in Youth and Young Adults With Cystic Fibrosis.

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2.  Continuous Glucose Monitoring and HbA1c in Cystic Fibrosis: Clinical Correlations and Implications for CFRD Diagnosis.

Authors:  Kevin J Scully; Jordan S Sherwood; Kimberly Martin; Melanie Ruazol; Peter Marchetti; Mary Larkin; Hui Zheng; Gregory S Sawicki; Ahmet Uluer; Isabel Neuringer; Lael M Yonker; Leonard Sicilian; Deborah J Wexler; Melissa S Putman
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3.  The Relationship Between Continuous Glucose Monitoring and OGTT in Youth and Young Adults With Cystic Fibrosis.

Authors:  Christine L Chan; Laura Pyle; Tim Vigers; Philip S Zeitler; Kristen J Nadeau
Journal:  J Clin Endocrinol Metab       Date:  2022-01-18       Impact factor: 6.134

4.  Continuous glucose monitoring in youth with cystic fibrosis treated with lumacaftor-ivacaftor.

Authors:  Angel Li; Tim Vigers; Laura Pyle; Edith Zemanick; Kristen Nadeau; Scott D Sagel; Christine L Chan
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5.  Clinical practice versus guidelines for the screening of cystic fibrosis-related diabetes: A French survey from the 47 centers.

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6.  Practical aspects of diabetes technology use: Continuous glucose monitors, insulin pumps, and automated insulin delivery systems.

Authors:  Brynn E Marks; Kristen M Williams; Jordan S Sherwood; Melissa S Putman
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7.  Cystic fibrosis-related diabetes: Prevalence, screening, and diagnosis.

Authors:  Swapnil Khare; Marisa Desimone; Nader Kasim; Christine L Chan
Journal:  J Clin Transl Endocrinol       Date:  2021-12-07

8.  Delayed glucose peak and elevated 1-hour glucose on the oral glucose tolerance test identify youth with cystic fibrosis with lower oral disposition index.

Authors:  Kalie L Tommerdahl; John T Brinton; Tim Vigers; Melanie Cree-Green; Philip S Zeitler; Kristen J Nadeau; Christine L Chan
Journal:  J Cyst Fibros       Date:  2020-09-11       Impact factor: 5.482

9.  Hyperglycaemia in cystic fibrosis adversely affects BK channel function critical for mucus clearance.

Authors:  Charles D Bengtson; Michael D Kim; Abeer Anabtawi; Jianghua He; John S Dennis; Sara Miller; Makoto Yoshida; Nathalie Baumlin; Matthias Salathe
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10.  Continuous Glucose Monitoring as a Valuable Tool in the Early Detection of Diabetes Related to Cystic Fibrosis.

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Journal:  Front Pediatr       Date:  2021-07-09       Impact factor: 3.418

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