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

Systematic Reviews
Laura BirchRachel Perry

Abstract

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 inter...Continue Reading

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May 17, 2019·Expert Review of Respiratory Medicine·Carla ColomboGianfranco Alicandro
Jul 12, 2020·Journal of Pediatric Endocrinology & Metabolism : JPEM·Crésio AlvesCristiano Tulio Maciel Albuquerque

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