Almers Lucy M, Graham James E, Havel Peter J, Corley Douglas A
Division of Research, Kaiser Permanente, Oakland, California.
Department of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, California; Department of Nutrition, University of California, Davis, California.
Clin Gastroenterol Hepatol. 2015 Dec;13(13):2256-64.e1-3. doi: 10.1016/j.cgh.2015.01.009. Epub 2015 Jan 26.
BACKGROUND & AIMS: Abdominal obesity and increasing body mass index are risk factors for esophageal adenocarcinoma and its main precursor, Barrett's esophagus; however, there are no known biological mechanisms for these associations or regarding why only some patients with gastroesophageal reflux disease develop Barrett's esophagus. We evaluated the association between Barrett's esophagus and multimers of an adipose-associated hormone, adiponectin.
We conducted a case-control study evaluating the associations between adiponectin (total, high-molecular-weight, and low-/medium-molecular-weight) and Barrett's esophagus within the Kaiser Permanente Northern California population. Patients with a new diagnosis of Barrett's esophagus (cases) were matched to patients with gastroesophageal reflux disease (GERD) without Barrett's esophagus and to population controls.
Complete serologic and epidemiologic data were available for 284 cases, 294 GERD controls, and 285 population controls. Increasing adiponectin levels were a risk factor for Barrett's esophagus among patients with GERD (total adiponectin fourth vs first quartile odds ratio [OR], 1.96; 95% confidence interval [CI], 1.17-3.27; high-molecular-weight adiponectin OR, 1.65; 95% CI, 1.00-2.73; low-/medium-molecular-weight adiponectin OR, 2.18; 95% CI, 1.33-3.56), but not compared with population controls. The associations were significantly stronger among patients reporting frequent GERD symptoms and among smokers (P values interaction < .01).
Adiponectin levels are associated positively with the risk of Barrett's esophagus among patients with GERD and among smokers, but not among population controls without GERD symptoms. Higher adiponectin concentrations either independently may contribute to the aberrant healing of esophageal injury into Barrett's esophagus or be a marker for other factors.
腹部肥胖和体重指数增加是食管腺癌及其主要前驱病变巴雷特食管的危险因素;然而,这些关联的生物学机制以及为何只有部分胃食管反流病患者会发展为巴雷特食管尚不清楚。我们评估了巴雷特食管与一种脂肪相关激素脂联素多聚体之间的关联。
我们进行了一项病例对照研究,评估脂联素(总脂联素、高分子量脂联素和低/中分子量脂联素)与北加利福尼亚凯撒医疗集团人群中巴雷特食管之间的关联。新诊断为巴雷特食管的患者(病例组)与无巴雷特食管的胃食管反流病(GERD)患者及人群对照进行匹配。
共有284例病例、294例GERD对照和285例人群对照获得了完整的血清学和流行病学数据。在GERD患者中,脂联素水平升高是巴雷特食管的危险因素(总脂联素第四分位数与第一分位数比值比[OR]为1.96;95%置信区间[CI]为1.17 - 3.27;高分子量脂联素OR为1.65;95% CI为1.00 - 2.73;低/中分子量脂联素OR为2.18;95% CI为1.33 - 3.56),但与人群对照相比无此关联。在报告频繁GERD症状的患者和吸烟者中,这种关联显著更强(P值交互作用<0.01)。
脂联素水平在GERD患者和吸烟者中与巴雷特食管风险呈正相关,但在无GERD症状的人群对照中无此关联。较高的脂联素浓度可能独立地促成食管损伤异常愈合为巴雷特食管,或者是其他因素的标志物。