Glycated Hemoglobin, A Potential Screening Tool for Cystic Fibrosis Related Diabetes
Cystic Fibrosis Related Diabetes(CFRD) is associated with an increased risk of early mortality, increasing from 40% to 75% before 30 years of age. In recent decades, the median life expectancy of patients with cystic fibrosis (CF) has increased. Although studies have shown that exocrine pancreatic insufficiency (PI) and increasing age are 2 risk factors for CFRD, 10% of patients with CF already have CFRD by 10 years of age.
In a study, researchers have reported that glycated haemoglobin (A1C) cutoffs allow early identification of children requiring further CFRD investigations, which may reduce the clinical burden of children with CF. The study findings were published in the Canadian Journal of Diabetes on March 25, 2021.
A recent study carried out by Gilmour et al, suggested a stepwise approach as a first-line screening method for CFRD in adults with CF. It was concluded that only patients with A1C levels between 5.5% and 6.4% should undertake an OGTT annually. However, it has never been tested in patients <18 years of age. Therefore, Dr Geneviève Mailhot and her team conducted a study to document the screening rate for cystic fibrosis-related diabetes (CFRD) in children followed at cystic fibrosis (CF) clinic in Canada. They further evaluated the accuracy of various glycated haemoglobin (A1C) cutoffs to screen for CFRD and impaired glucose tolerance (IGT) in a pediatric CF population.
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