Association of adiponectin multimers with Barrett’s oesophagus

Objective:Barrett’s oesophagus is associated with abdominal obesity. Adiponectin is a peptide that is secreted from adipocytes and circulates in three multimeric forms: low molecular weight (LMW), middle molecular weight (MMW), and high molecular weight (HMW). The anti-inflammatory effects of adipon...

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Veröffentlicht in:Gut 2009-12, Vol.58 (12), p.1583-1589
Hauptverfasser: Rubenstein, J H, Kao, J Y, Madanick, R D, Zhang, M, Wang, M, Spacek, M B, Donovan, J L, Bright, S D, Shaheen, N J
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Sprache:eng
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Zusammenfassung:Objective:Barrett’s oesophagus is associated with abdominal obesity. Adiponectin is a peptide that is secreted from adipocytes and circulates in three multimeric forms: low molecular weight (LMW), middle molecular weight (MMW), and high molecular weight (HMW). The anti-inflammatory effects of adiponectin are specific to individual multimers, with LMW being most anti-inflammatory. We postulated that circulating levels of adiponectin and its multimers would be associated with the risk of Barrett’s oesophagus.Design:Cross-sectional study.Setting:Outpatient clinic in North Carolina, USA.Patients:Cases of Barrett’s oesophagus and controls undergoing upper endoscopy for gastro-oesophageal reflux disease (GORD).Main outcome measures:Adjusted odds ratios of plasma adiponectin levels and its multimers for Barrett’s oesophagus.Results:There were 112 cases of Barrett’s oesophagus and 199 GORD controls. Total adiponectin was not associated with Barrett’s oesophagus (3rd tertile vs 1st tertile adjusted odds ratio (aOR)  = 0.88; 95% confidence interval (CI)  = 0.44 to 1.78). High levels of LMW adiponectin were associated with a decreased risk of Barrett’s oesophagus (3rd tertile vs 1st tertile aOR = 0.33; 95% CI, 0.16 to 0.69), and a high LMW/total ratio appeared particularly inversely associated with Barrett’s oesophagus (3rd tertile vs 1st tertile aOR = 0.27; 95% CI, 0.13 to 0.58).Conclusions:High levels of LMW adiponectin are associated with a decreased risk of Barrett’s oesophagus among patients with GORD. Further human studies are required to confirm these findings, and in vitro studies are needed to understand if there is a mechanism whereby adiponectin may affect Barrett’s metaplasia.
ISSN:0017-5749
1468-3288
DOI:10.1136/gut.2008.171553