Cystic Fibrosis related diabetes (CFRD), a major factor of morbid-mortality in CF, is characterized by a preclinical phase of glucose intolerance particularly long reaching up to 10 years. At the physiopathology level, insulin secretion is determinant in the glucose tolerance abnormalities in CF. Indeed insulin secretion is dependent of the CFTR activity at the beta cell surface and inhibition of CFTR leads to a decrease in insulin secretion. Recently, the combination of the lumacaftor, a CFTR corrector, with Ivacaftor, a CFTR potentiator, was studied in patient with CF homozygous for the Phe508 del CFTR mutation patients and showed an improvement of the respiratory state in comparison with the placebo group. These data suggests that lumacaftor in combination with ivacaftor in targeting CFTR action may have an early impact on the insulin-secretion and consequently on the glucose tolerance.
Study Type
OBSERVATIONAL
Enrollment
55
Lumacaftor-Ivacaftor treatment during one year
Hôpitaux Universitaires de Strasbourg
Strasbourg, Alsace, France
Centre Hospitalier Universitaire d'Angers
Angers, France
Hôpital Renée Sabran
Giens, France
Centre Hospitalier Lyon Sud
Lyon, France
Hôpital NORD - Assistance Publique Hôpitaux de Marseille
Marseille, France
Hôpital Arnaud de Villeneuve
Montpellier, France
Hôpital Robert Debré
Paris, France
American Memorial Hospital
Reims, France
Clinique "Mucoviscidose" Presqu'île de Perharidy
Roscoff, France
Hôpital Charles Nicolle
Rouen, France
...and 3 more locations
Measure of 2 hours plasma glucose value (mmol/l) of OGTT, change from baseline at one year of Lumacaftor-Ivacaftor treatment
Time frame: Day 0 (traitement beginning) and year 1
Fasting and one hour glucose value of OGTT (mmol/l)
Time frame: Day 0 (traitement beginning) and year 1
C peptide and insulin values at T0, 1 , 2 hours of OGTT (µg/l)
Time frame: Day 0 (traitement beginning) and year 1
Glucose, insulin and C peptide AUC of OGTT (µU/L)
Time frame: Day 0 (traitement beginning) and year 1
HOMA -R , HOMA-S
Time frame: Day 0 (traitement beginning) and year 1
Mean glucose value per day and 2 h after meal (mg/dl)
Time frame: Day 0 (traitement beginning) and year 1
Duration in hypoglycemic area [hypo CGM = 2 consecutive values below 3.3 mmol/l - % of time spent]
Time frame: Day 0 (traitement beginning) and year 1
Duration in hyperglycemic area [for glucose value higher than 7.7 mmol/l, % time /24h]
Number hypoglycaemic events (below 3.3mmol/L, from midnight to 6 am) Variability glycemic indexes: MAGE (mg/dl), SD (mg/dl)
Time frame: Day 0 (traitement beginning) and year 1
Number hypoglycaemic events (below 3.3mmol/L, from midnight to 6 am)
Variability glycemic indexes: MAGE (mg/dl), SD (mg/dl)
Time frame: Day 0 (traitement beginning) and year 1
Variability glycemic indexes: MAGE (mg/dl), SD (mg/dl)
Time frame: Day 0 (traitement beginning) and year 1
HbA1c (mmol/l and %)
Time frame: Day 0 (traitement beginning) and year 1
Daily insulin doses (UI/day)
Time frame: Day 0 (traitement beginning) and year 1
(BMI) body mass index
Time frame: Day 0 (traitement beginning) and year 1
Weight (Kg) maximum weight never reached
Time frame: Day 0 (traitement beginning) and year 1
Albumin and Pre albumin (g/l)
Time frame: Day 0 (traitement beginning) and year 1
FEV1, Vital Capacity (VC) (L and %)
Time frame: Day 0 (traitement beginning) and year 1
O2 saturation (%)
Time frame: Day 0 (traitement beginning) and year 1
Number of cures of antibiotics IV and per os /year and interval between 2 cures (week)
Time frame: Day 0 (traitement beginning) and year 1
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.