Glucose tolerance in cystic fibrosis.
Open Access
- 1 May 1991
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 66 (5) , 612-616
- https://doi.org/10.1136/adc.66.5.612
Abstract
Glucose tolerance was evaluated in 356 living and dead patients with cystic fibrosis who were recorded at the Danish Cystic Fibrosis Centre. Twenty two patients (6%) were treated elsewhere, 25 (7%) were unable, unwilling or too young (age less than 2 years) to participate; 309 patients (87%) were therefore eligible for the study of whom 99 (32%) were dead and 210 (68%) were alive. Of the dead patients, 13 also had diabetes mellitus (13%). Of the living patients (median age 14 years, range 2-40), nine (4%) were known to have diabetes and all were being treated with insulin. In the remaining 201 patients an oral glucose tolerance test (1.75 g/kg body weight, maximum 75 g) was carried out. A total of 155 patients (74%) had normal glucose tolerance, 31 (15%) had impaired glucose tolerance, and 15 (7%) had diabetes mellitus according to the WHO criteria. The percentage of glycated haemoglobin (HbA1c) (reference range 4.1-6.4%) increased significantly as glucose tolerance decreased: when glucose tolerance was normal the median was 5.2%; when it was impaired the figure was 5.5%; in patients whose diabetes was diagnosed by the oral glucose tolerance test it was 5.9%; and in patients already known to have diabetes mellitus it was 8.6%. The incidence and prevalence of impaired glucose tolerance and diabetes mellitus increased with age. From the age of 15 to 30 years the decrease in the prevalence of normal glucose tolerance was almost linear. Within this age span the proportion of patients with cystic fibrosis with normal glucose tolerance was reduced by roughly 5%/year. Only 35% (95% confidence interval (CI) 22 to 48%) of the patients with cystic fibrosis who were alive at the age of 25 years had normal glucose tolerance; 32% (95% CI 14 to 49%) were diabetic. The prevalence of glucose intolerance in cystic fibrosis is rapidly increasing with age; its potentially harmful effect on the prognosis of cystic fibrosis is of increasing importance as the length of survival of these patients increases.Keywords
This publication has 34 references indexed in Scilit:
- LIVER DISEASE AND BILEDUCT ABNORMALITIES IN ADULTS WITH CYSTIC FIBROSISThe Lancet, 1989
- Diabetes and cystic fibrosis: New questions emerging from increased longevityThe Journal of Pediatrics, 1988
- Diabetes mellitus associated with cystic fibrosisPublished by Elsevier ,1988
- The Interaction of 2 DiseasesMedicine, 1986
- Progressive Nephropathy in a Patient with Cystic Fibrosis and DiabetesNew England Journal of Medicine, 1986
- Microangiopathy in a Young Adult with Cystic Fibrosis and Diabetes MellitusNew England Journal of Medicine, 1986
- Endokrine Pankreasfunktion bei Mukoviszidose*Klinische Padiatrie, 1985
- FREQUENT ANTIBIOTIC THERAPY IMPROVES SURVIVAL OF CYSTIC FIBROSIS PATIENTS WITH CHRONIC PSEUDOMONAS AERUGINOSA INFECTIONActa Paediatrica, 1983
- Cystic fibrosis in adultsThe American Journal of Medicine, 1979
- Pancreatic alpha and beta cell functions in cystic fibrosisThe Journal of Pediatrics, 1977