Cystic Fibrosis Related Diabetes Clinical Trial
Official title:
Microvascular Complications of Cystic Fibrosis Related Diabetes
Our general aim is to determine the prevalence of diabetic microvascular complications in CFRD patients with and without fasting hyperglycemia, and to explore whether the presence of these complications is related to diabetes or CF factors. This cross-sectional study will provide pilot data for a longitudinal study of diabetes complications in CF.
Microvascular complications of diabetes such as eye, kidney and nerve disease are common in
individuals with type 1 and type 2 diabetes, and are a source of significant morbidity and
mortality. Microvascular diabetes complications have been anecdotally reported in cystic
fibrosis related diabetes (CFRD), but their prevalence is unknown. 40% of adult CF patients
have CFRD, which shares features of both type 1 and type 2 diabetes but is a distinct
clinical entity (1). Many clinicians are reluctant to add the burden of aggressive diabetes
management to the already complex medical regimen of these patients. It is sometimes stated
that they will not live long enough to develop complications of diabetes. However, longevity
in CF has dramatically increased, and many patients now live into their thirties, forties,
and fifties. As they live longer, it becomes increasingly likely that at least some will
develop diabetes complications. A better understanding of this negative outcome would help
resolve the question of whether aggressive screening and management of diabetes is necessary
in CF.
As in other forms of diabetes, duration of diabetes and the magnitude of chronic
hyperglycemia are probably important determinants of microvascular complications in CFRD.
This information is not usually known at the time of presentation of CFRD because of the
insidious onset of the disease. Theoretically, CF pulmonary disease, including chronic
hypoxia and venous congestion related to pulmonary hypertension, may additionally aggravate
microvascular changes. However, the metabolic differences between CFRD and type 1 and type 2
diabetes may also serve to protect CF patients from some diabetes complications. At the time
diabetes complications develop, patients with type 1 and type 2 diabetes tend to have
concomitant obesity, hypertension, insulin resistance, hyperlipidemia and atherosclerotic
cardiovascular disease. These factors, which are generally absent in CF, may contribute to
the pathophysiology of microvascular complications in other forms of diabetes.
The University of Minnesota CF Center is in the unique position of having a
well-characterized diabetes population, since diabetes screening was instituted several
years ago as part of routine annual CF studies. In our population of 450 CF patients, 113
have been diagnosed with diabetes, and the remainder are known to have either normal or
impaired glucose tolerance. In addition to our CFRD experience, the University of Minnesota
has a strong background of experience in large population-based screening and intervention
trials concerning diabetes complications. Not only were we a participating center in the
NIH-sponsored multi-center Diabetes Control and Complications Trial (DCCT) (2) and the
current DCCT follow-up Epidemiology of Diabetes Interventions and Complications trial
(EDIC), but our laboratory was central reference laboratory for the DCCT and EDIC. Thus, our
physicians, nurses, biostatisticians, GCRC staff and laboratory staff are all quite
knowledgeable and experienced in the methods to be used in the present application.
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Time Perspective: Prospective
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