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IGF-1 and survival in ESRD.

AbstractBACKGROUND AND OBJECTIVES:
IGF-1 deficiency links to malnutrition in CKD patients; however, it is not clear to what extent it associates with survival among these patients.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS:
Serum IGF-1 and other biochemical, clinical (subjective global assessment), and densitometric (dual energy x-ray absorptiometry) markers of nutritional status and mineral and bone metabolism were measured in a cohort of 365 Swedish clinically stable CKD stage 5 patients (median age of 53 years) initiating dialysis between 1994 and 2009; in 207 patients, measurements were also taken after 1 year of dialysis. Deaths were registered during a median follow-up of 5 years. Associations of mortality with baseline IGF-1 and changes of IGF-1 after 1 year of dialysis were evaluated by Cox models.
RESULTS:
At baseline, IGF-1 concentrations associated negatively with age, diabetes mellitus, cardiovascular disease, poor nutritional status, IL-6, and osteoprotegerin and positively with body fat mass, bone mineral density, serum phosphate, calcium, and fibroblast growth factor-23. At 1 year, IGF-1 had increased by 33%. In multivariate regression, low age, diabetes mellitus, and high serum phosphate and calcium associated with IGF-1 at baseline, and in a mixed model, these factors, together with high fat body mass, associated with changes of IGF-1 during the first 1 year of dialysis. Adjusting for calendar year of inclusion, age, sex, diabetes mellitus, cardiovascular disease, IL-6, and poor nutritional status, a 1 SD higher level of IGF-1 at baseline associated with lower mortality risk (hazard ratio, 0.57; 95% confidence interval, 0.32 to 0.98). Persistently low or decreasing IGF-1 levels during the first 1 year on dialysis predicted worse survival (adjusted hazard ratio, 2.19; 95% confidence interval, 1.06 to 4.50).
CONCLUSION:
In incident dialysis patients, low serum IGF-1 associates with body composition and markers of mineral and bone metabolism, and it predicts increased mortality risk.
AuthorsTing Jia, Thiane Gama Axelsson, Olof Heimbürger, Peter Bárány, Bengt Lindholm, Peter Stenvinkel, Abdul Rashid Qureshi
JournalClinical journal of the American Society of Nephrology : CJASN (Clin J Am Soc Nephrol) Vol. 9 Issue 1 Pg. 120-7 (Jan 2014) ISSN: 1555-905X [Electronic] United States
PMID24178975 (Publication Type: Journal Article, Observational Study, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • IGF1 protein, human
  • Insulin-Like Growth Factor I
Topics
  • Adult
  • Aged
  • Biomarkers (blood)
  • Body Composition
  • Bone Remodeling
  • Chi-Square Distribution
  • Cross-Sectional Studies
  • Down-Regulation
  • Female
  • Humans
  • Insulin-Like Growth Factor I (analysis)
  • Kaplan-Meier Estimate
  • Kidney Failure, Chronic (blood, diagnosis, mortality, therapy)
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Nutritional Status
  • Proportional Hazards Models
  • Renal Dialysis
  • Risk Factors
  • Sweden (epidemiology)
  • Time Factors
  • Treatment Outcome

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