An Update in Cystic Fibrosis-Related Diabetes in Children and Adolescents.
Dana-Teodora Anton-PaduraruAlina Mariela MurguMădălina Andreea DonosFelicia TrofinAlice Nicoleta AzoicăiPaula PopoviciAurelian Bogdan StanaIonela GheorghiescuLaura Mihaela TrandafirPublished in: Children (Basel, Switzerland) (2023)
This paper delineates several aspects of cystic fibrosis-related diabetes (CFRD)-a common complication of cystic fibrosis (CF). CFRD exhibits a predilection for older individuals with CF, yet it also extends its influence on children and adolescents. Scientific insights postulate a potential link between CFRD and the aberrant mucus production within the pancreas, thereby culminating in pancreatic insufficiency. This, in turn, perturbs the synthesis of insulin, a pivotal endocrine hormone responsible for the regulation of glycemic levels. Standardized protocols advocate for the systematic screening of CFRD among all individuals with CF, commencing at the age of 10 years using the oral glucose tolerance test (OGTT). Therapeutic modalities encompass insulin therapy, dietary adjustments, and the vigilant monitoring of glycemic parameters. The overarching objective is to maintain blood glucose levels within a targeted range to mitigate the advent of diabetic complications. Untreated or sub-optimally managed CFRD can precipitate a spectrum of deleterious health ramifications, encompassing cardiovascular afflictions, neuropathy, renal dysfunction, and ocular complications.
Keyphrases
- cystic fibrosis
- glycemic control
- type diabetes
- blood glucose
- pseudomonas aeruginosa
- lung function
- insulin resistance
- weight loss
- risk factors
- public health
- healthcare
- cardiovascular disease
- oxidative stress
- blood pressure
- metabolic syndrome
- mesenchymal stem cells
- physical activity
- community dwelling
- human health
- chronic obstructive pulmonary disease
- risk assessment
- air pollution
- climate change
- living cells
- optic nerve