Background
In the general population, circulating adiponectin is associated with a favorable cardiovascular risk profile (e.g., lower triglycerides and body fat) and decreased mortality. Hemodialysis (HD) patients have comparatively higher adiponectin concentrations, but prior studies examining the adiponectin-mortality association in this population have not accounted for body composition nor shown a consistent relationship.
Study Design
Prospective cohort study.
Settings and Participants
We examined baseline serum adiponectin concentrations in 501 HD patients across 13 dialysis centers from the prospective MADRAD (Malnutrition, Diet, and Racial Disparities in Chronic Kidney Disease) cohort (entry period 10/2011-2/2013, follow-up through 8/2013).
Predictor
Serum adiponectin concentration in tertiles (Tertiles 1, 2, and 3 defined as <=16.1, >16.1–30.1, >30.1–100.0 ug/ml, respectively). Adjustment variables included case-mix and laboratory tests (age, sex, race, ethnicity, vintage, diabetes, serum albumin, total iron binding capacity, serum creatinine, white blood cell count, phosphate, hemoglobin, normalized protein catabolic rate), body composition surrogates (subcutaneous, visceral, and total body fat; lean body mass), and serum lipid levels (cholesterol, HDL, triglycerides).
Outcomes
All-cause mortality using survival (Cox) models incrementally adjusted for case-mix and laboratory tests.
Results
Among 501 HD patients, 50 deaths were observed during 631.1 person-years of follow-up time. In case-mix– and laboratory-adjusted Cox analyses, the highest adiponectin tertile was associated with increased mortality vs. the lowest tertile (HR, 3.35; 95% CI, 1.50–7.47). These associations were robust in analyses that additionally accounted for body composition (HR, 3.18; 95% CI, 1.61–8.24) and lipids (HR, 3.64; 95% CI, 1.34–7.58).
Limitations
Residual confounding cannot be excluded.
Conclusions
In conclusion, higher adiponectin is associated with a 3-fold higher death risk in HD patients independent of body composition and lipids. Future studies are needed to elucidate underlying mechanisms, and to determine therapeutic targets associated with improved outcomes in HD patients.