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Published in: Systematic Reviews 1/2018

Open Access 01-12-2018 | Protocol

Dietary interventions for managing glucose abnormalities in cystic fibrosis: a systematic review protocol

Published in: Systematic Reviews | Issue 1/2018

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Abstract

Background

Glucose abnormalities in cystic fibrosis (CF) are common, but there is limited evidence to guide their dietary management. Progressive impaired glucose tolerance eventually leads to cystic fibrosis-related diabetes (CFRD), the most prevalent complication of CF, which is associated with increased morbidity and mortality. Optimising glycaemic control improves clinical status and reduces mortality; insulin therapy is the primary means of controlling glycaemia in CFRD, but its role in managing pre-diabetes is less clear. CF dietary therapy requires a high calorie diet due to increased energy expenditure and malabsorption, but this energy-dense diet is typically high in fat and sugar, and high sugar intakes often result in hyperglycaemia in individuals who have impaired glucose handling. Current guidelines for the dietary management of glucose abnormalities in CF are based on clinical consensus rather than empirical evidence. A systematic review conducted in 2012 on the effects of low glycaemic index dietary intervention in CF concluded that there is a dearth of evidence in this area. This review will update the systematic review by Balzer et al. in 2012 and will broaden the scope of their review to include any type of dietary intervention for managing glucose abnormalities in CF.

Methods

Quantitative studies of dietary interventions to manage glucose abnormalities in individuals aged over 5 years with CF and glucose abnormalities will be reviewed. No limits will be placed on language or study design. The comparator will be standard CF dietary therapy (energy dense, high-fat diet) in addition to insulin therapy for individuals with CFRD. Electronic databases will be searched for completed quantitative studies published in peer-review journals that focus on dietary interventions for managing glucose abnormalities in CF. Searches will be conducted from 2000 up to the present day to reflect the evolving improvements in CF management. No restrictions will be placed on study design or language. Duration of the dietary intervention must be a minimum of 2 months and only interventions in out-patient or community settings will be included. Studies must report on dietary intervention, glycaemic control, anthropometry and lung function. Evidence will be assessed for heterogeneity and a narrative review or meta-analysis conducted as appropriate.

Discussion

This systematic review will elucidate current knowledge of the effects of dietary interventions for managing glucose abnormalities in the vulnerable CF clinical population.

Systematic review registration

Appendix
Available only for authorised users
Footnotes
1
The applicability of HbA1c in the CF population is controversial due to increased red blood cell turnover [3] but will be included in this review to be as inclusive as possible.
 
2
Exploratory outcome is not a validated definition of diabetes
 
Literature
1.
go back to reference Filbrun AG, Lahiri T, Ren CL. Handbook of cystic fibrosis. Switzerland: Springer International Publishing; 2016. Filbrun AG, Lahiri T, Ren CL. Handbook of cystic fibrosis. Switzerland: Springer International Publishing; 2016.
2.
go back to reference Bismuth E, et al. Glucose tolerance and insulin secretion, morbidity, and death in patients with cystic fibrosis. J Pediatr. 2008;152(4):540–5.CrossRefPubMed Bismuth E, et al. Glucose tolerance and insulin secretion, morbidity, and death in patients with cystic fibrosis. J Pediatr. 2008;152(4):540–5.CrossRefPubMed
4.
go back to reference Moran A, et al. Management of cystic fibrosis-related diabetes in children and adolescents. Pediatr Diabetes. 2014;15(Suppl 20):65–76.CrossRefPubMed Moran A, et al. Management of cystic fibrosis-related diabetes in children and adolescents. Pediatr Diabetes. 2014;15(Suppl 20):65–76.CrossRefPubMed
5.
7.
go back to reference Rodman HM, Doershuk CF, Roland JM. The interaction of 2 diseases: diabetes mellitus and cystic fibrosis. Medicine. 1986;65(6):389–98.CrossRefPubMed Rodman HM, Doershuk CF, Roland JM. The interaction of 2 diseases: diabetes mellitus and cystic fibrosis. Medicine. 1986;65(6):389–98.CrossRefPubMed
8.
go back to reference Castellani C, et al. ECFS best practice guidelines: the 2018 revision. J Cyst Fibros. 2018;17(2):153–78.CrossRefPubMed Castellani C, et al. ECFS best practice guidelines: the 2018 revision. J Cyst Fibros. 2018;17(2):153–78.CrossRefPubMed
9.
go back to reference Rosenecker J, et al. Diabetes mellitus and cystic fibrosis: comparison of clinical parameters in patients treated with insulin versus oral glucose-lowering agents. Pediatr Pulmonol. 2001;32(5):351–5.CrossRefPubMed Rosenecker J, et al. Diabetes mellitus and cystic fibrosis: comparison of clinical parameters in patients treated with insulin versus oral glucose-lowering agents. Pediatr Pulmonol. 2001;32(5):351–5.CrossRefPubMed
10.
go back to reference Wilson D, et al. Challenges in the dietary treatment of cystic fibrosis related diabetes mellitus. Clin Nutr. 2000;19(2):87–93.CrossRefPubMed Wilson D, et al. Challenges in the dietary treatment of cystic fibrosis related diabetes mellitus. Clin Nutr. 2000;19(2):87–93.CrossRefPubMed
11.
go back to reference Chamnan P, et al. Diabetes as a determinant of mortality in cystic fibrosis. Diabetes Care. 2010;33(2):311–6.CrossRefPubMed Chamnan P, et al. Diabetes as a determinant of mortality in cystic fibrosis. Diabetes Care. 2010;33(2):311–6.CrossRefPubMed
12.
go back to reference Mohan K, et al. Mechanisms of glucose intolerance in cystic fibrosis. Diabet Med. 2009;26(6):582–8.CrossRefPubMed Mohan K, et al. Mechanisms of glucose intolerance in cystic fibrosis. Diabet Med. 2009;26(6):582–8.CrossRefPubMed
13.
go back to reference Finkelstein SM, et al. Diabetes mellitus associated with cystic fibrosis. J Pediatr. 1988;112(3):373–7.CrossRefPubMed Finkelstein SM, et al. Diabetes mellitus associated with cystic fibrosis. J Pediatr. 1988;112(3):373–7.CrossRefPubMed
14.
go back to reference Rana M, et al. Cystic fibrosis-related diabetes in children—gaps in the evidence? Nat Rev Endocrinol. 2010;6(7):371–8.CrossRefPubMed Rana M, et al. Cystic fibrosis-related diabetes in children—gaps in the evidence? Nat Rev Endocrinol. 2010;6(7):371–8.CrossRefPubMed
15.
go back to reference White H, et al. Nutritional decline in cystic fibrosis related diabetes: the effect of intensive nutritional intervention. J Cyst Fibros. 2009;8(3):179–85.CrossRefPubMed White H, et al. Nutritional decline in cystic fibrosis related diabetes: the effect of intensive nutritional intervention. J Cyst Fibros. 2009;8(3):179–85.CrossRefPubMed
17.
go back to reference Craig M, et al. National evidence-based clinical care guidelines for type 1 diabetes in children, adolescents and adults, vol. 346. Canberra: Australian Government Department of Health and Ageing; 2011. Craig M, et al. National evidence-based clinical care guidelines for type 1 diabetes in children, adolescents and adults, vol. 346. Canberra: Australian Government Department of Health and Ageing; 2011.
18.
go back to reference American Diabetes Association. 4. Lifestyle management: standards of medical Care in Diabetes—2018. Diabetes Care. 2018;41(Supplement 1):S38–50.CrossRef American Diabetes Association. 4. Lifestyle management: standards of medical Care in Diabetes—2018. Diabetes Care. 2018;41(Supplement 1):S38–50.CrossRef
19.
go back to reference Dyson P, et al. Diabetes UK evidence-based nutrition guidelines for the prevention and management of diabetes. Diabet Med. 2011;28(11):1282–8.CrossRefPubMed Dyson P, et al. Diabetes UK evidence-based nutrition guidelines for the prevention and management of diabetes. Diabet Med. 2011;28(11):1282–8.CrossRefPubMed
20.
go back to reference Balzer BW, et al. Low glycaemic index dietary interventions in youth with cystic fibrosis: a systematic review and discussion of the clinical implications. Nutrients. 2012;4(4):286–96.CrossRefPubMedPubMedCentral Balzer BW, et al. Low glycaemic index dietary interventions in youth with cystic fibrosis: a systematic review and discussion of the clinical implications. Nutrients. 2012;4(4):286–96.CrossRefPubMedPubMedCentral
21.
22.
go back to reference American Diabetes Association. 2. Classification and diagnosis of diabetes: standards of medical care in Diabetes—2018. Diabetes Care. 2018;41(Supplement 1):S13–27.CrossRef American Diabetes Association. 2. Classification and diagnosis of diabetes: standards of medical care in Diabetes—2018. Diabetes Care. 2018;41(Supplement 1):S13–27.CrossRef
23.
go back to reference Hameed S, et al. Early glucose abnormalities in cystic fibrosis are preceded by poor weight gain. Diabetes Care. 2010;33(2):221–6.CrossRefPubMed Hameed S, et al. Early glucose abnormalities in cystic fibrosis are preceded by poor weight gain. Diabetes Care. 2010;33(2):221–6.CrossRefPubMed
26.
go back to reference Guyatt GH, et al. GRADE guidelines: a new series of articles in the journal of clinical epidemiology. J Clin Epidemiol. 2011;64(4):380–2.CrossRefPubMed Guyatt GH, et al. GRADE guidelines: a new series of articles in the journal of clinical epidemiology. J Clin Epidemiol. 2011;64(4):380–2.CrossRefPubMed
Metadata
Title
Dietary interventions for managing glucose abnormalities in cystic fibrosis: a systematic review protocol
Publication date
01-12-2018
Published in
Systematic Reviews / Issue 1/2018
Electronic ISSN: 2046-4053
DOI
https://doi.org/10.1186/s13643-018-0757-y

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