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Part 9: Miscellaneous Complications and Pathophysiologic Mechanisms |
Division of Pediatric Nephrology,1 Oregon Health and Science University, Portland, Oregon, and Division of Pediatric Nephrology,2 University of California at San Diego, La Jolla, California, U.S.A.
Correspondence to: R.H. Mak, Division of Pediatric Nephrology, University of California at San Diego, 9500 Gilman Drive, MC 0831, La Jolla, California 92093-0831 U.S.A. romak{at}ucsd.edu
Cachexia is common in end-stage renal disease (ESRD) patients, and it is
an important risk factor for poor quality of life and increased mortality and
morbidity. Chronic inflammation is an important cause of cachexia in ESRD
patients. In the present review, we examine recent evidence suggesting that
adipokines or adipocytokines such as leptin, adiponectin, resistin, tumor
necrosis factor
, interleukin-6, and interleukin-1β may play
important roles in uremic cachexia. We also review the physiology and the
potential roles of gut hormones, including ghrelin, peptide YY, and
cholecystokinin in ESRD. Understanding the molecular pathophysiology of these
novel hormones in ESRD may lead to novel therapeutic strategies.
KEY WORDS: Inflammation; cachexia; end-stage renal disease; ESRD; adipokines; ghrelin; peptide YY; cholecystokinin.
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