Active ghrelin levels and active to total ghrelin ratio in cancer-induced cachexia

Josè M. Garcia, Mariana Garcia-Touza, Rabih A. Hijazi, George Taffet, Daniel Epner, Douglas Mann, Roy G. Smith, Glenn R. Cunningham, Marco Marcelli

Research output: Contribution to journalArticle

195 Scopus citations

Abstract

Anorexia and weight loss are negative prognostic factors in patients with cancer. Although total ghrelin levels are increased in energy-negative states, levels of the biologically active octanoylated ghrelin and the anorexigenic peptide YY (PYY) have not been reported in patients with cancer-induced cachexia. We hypothesized that abnormal ghrelin and/or PYY levels contribute to cancer-induced cachexia. We evaluated 21 patients with cancer-induced cachexia; 24 cancer patients without cachexia; and 23 age-, sex-, race-, and BMI-matched subjects without cancer. Active ghrelin levels and the active to total ghrelin ratio were significantly increased in subjects with cancer-induced cachexia, compared with cancer and noncancer controls. PYY levels were similar among groups. Appetite measured by a visual analog scale was not increased in subjects with cachexie. The increase in active ghrelin levels is likely to be a compensatory response to weight loss. Cachexia may be a state of ghrelin resistance because appetite does not correlate with ghrelin levels. Changes in the active to total ghrelin ratio suggest that a mechanism other than increased secretion must be responsible for the increase in active ghrelin levels. PYY is unlikely to play an important role in cancer-induced cachexia.

Original languageEnglish
Pages (from-to)2920-2926
Number of pages7
JournalJournal of Clinical Endocrinology and Metabolism
Volume90
Issue number5
DOIs
StatePublished - May 1 2005
Externally publishedYes

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    Garcia, J. M., Garcia-Touza, M., Hijazi, R. A., Taffet, G., Epner, D., Mann, D., Smith, R. G., Cunningham, G. R., & Marcelli, M. (2005). Active ghrelin levels and active to total ghrelin ratio in cancer-induced cachexia. Journal of Clinical Endocrinology and Metabolism, 90(5), 2920-2926. https://doi.org/10.1210/jc.2004-1788