Cystic fibrosis (CF) is a genetic disorder characterized by chronic respiratory infections and pancreatic insufficiency. Growth fialure occurs in approximately 25% of patients with CF and is associated with more severe respiratory disease and decreased survival. Successful nutritional rehabilitation has been shown to improve respiratory status, decrease hospitalizations for pulmonary exacerbations and improve energy level. Megestrol acetate is a synthetic progestational hormone that has been shown to increase appetite and promote weight gain in patients with HIV/AIDS and certain forms of cancer. At the UAB CF Center 5 patients (3 females and 2 males; 12-28 years) received megestrol acetate for CF related growth failure. All 5 subjects have had a significant increase in appetite and associated weight gain, 3.3 to 8.4 kg (5-20% above pretreatment weight). All patients had an incrase in energy level, an increase in daily activity level and improved body image. Side effects were minor and resolved with decreasing megestrol acetate dose. We propose to evalute megestrol acetate in a randomized, double-blinded placebo controlled study to examine the effectiveness and safety of megestrol acetate therapy in patients with CF related growth failure. Primary outcome measurement will be weight gain; secondary outcome measurements will include caloric intake, body composition, quality of well being and pulmonary function.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Yu, Alan S L; Shen, Chengli; Landsittel, Douglas P et al. (2018) Baseline total kidney volume and the rate of kidney growth are associated with chronic kidney disease progression in Autosomal Dominant Polycystic Kidney Disease. Kidney Int 93:691-699
Askie, Lisa M; Darlow, Brian A; Finer, Neil et al. (2018) Association Between Oxygen Saturation Targeting and Death or Disability in Extremely Preterm Infants in the Neonatal Oxygenation Prospective Meta-analysis Collaboration. JAMA 319:2190-2201
McKenzie, Katelyn A; El Ters, Mirelle; Torres, Vicente E et al. (2018) Relationship between caffeine intake and autosomal dominant polycystic kidney disease progression: a retrospective analysis using the CRISP cohort. BMC Nephrol 19:378
Srinivasan, Lakshmi; Page, Grier; Kirpalani, Haresh et al. (2017) Genome-wide association study of sepsis in extremely premature infants. Arch Dis Child Fetal Neonatal Ed 102:F439-F445
Morrison, Shannon A; Goss, Amy M; Azziz, Ricardo et al. (2017) Peri-muscular adipose tissue may play a unique role in determining insulin sensitivity/resistance in women with polycystic ovary syndrome. Hum Reprod 32:185-192
Shen, Chengli; Landsittel, Douglas; Irazabal, María V et al. (2017) Performance of the CKD-EPI Equation to Estimate GFR in a Longitudinal Study of Autosomal Dominant Polycystic Kidney Disease. Am J Kidney Dis 69:482-484
Denson, Lee A; McDonald, Scott A; Das, Abhik et al. (2017) Early Elevation in Interleukin-6 is Associated with Reduced Growth in Extremely Low Birth Weight Infants. Am J Perinatol 34:240-247
Kline, Timothy L; Korfiatis, Panagiotis; Edwards, Marie E et al. (2017) Image texture features predict renal function decline in patients with autosomal dominant polycystic kidney disease. Kidney Int 92:1206-1216
James, Jennifer; Munson, David; DeMauro, Sara B et al. (2017) Outcomes of Preterm Infants following Discussions about Withdrawal or Withholding of Life Support. J Pediatr 190:118-123.e4
Younge, Noelle; Goldstein, Ricki F; Bann, Carla M et al. (2017) Survival and Neurodevelopmental Outcomes among Periviable Infants. N Engl J Med 376:617-628

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