Zhang Jinhua, Li Kangli, Pan Lingling, Teng Fei, Zhang Peizhen, Lin Bingquan, Yuan Youwen, Wei Xueyun, Li Wenyuan, Zhang Huijie
Key Laboratory of Functional and Clinical Translational Medicine, Department of General Medicine, Xiamen Medical College, Xiamen, China.
Department of Endocrinology and Metabolism, Tongji Hospital, Tongji University, Shanghai, China.
BMC Gastroenterol. 2021 Mar 21;21(1):131. doi: 10.1186/s12876-021-01721-9.
As a secreted adipokine, adipsin has been recently shown to play a pivotal role in metabolic disorders. However, information regarding the association of circulating adipsin with non-alcoholic fatty liver disease (NAFLD) in humans is scant.
We recruited 1163 obese adult subjects with waist circumference at least 90 cm in men and 80 cm in women from the community. Circulating adipsin levels were measured by enzyme-linked immunosorbent assay.
Circulating adipsin levels of NAFLD subjects was decreased compared to those in non-NAFLD (p < 0.05). The prevalence of NAFLD with lower levels of serum adipsin was significantly higher than those with higher values (57.6% vs. 50.9%, p < 0.05). Circulating adipsin levels were significantly associated with decreasing levels of fasting glucose and postprandial glucose (both p < 0.001 for interaction) in NAFLD subjects but not in non-NAFLD subjects. The risk of NAFLD was significantly decreased by 21.7% [OR (95% CI): 0.783 (0.679-0.902), p < 0.001], adjusting for age, gender, current smoking, alcohol consumption, physical activity, BMI, systolic BP, fasting glucose, total cholesterol, HDL-c, HOMA-IR, and body fat mass. Importantly, subjects in the lowest quartile of circulating adipsin were 1.88 times more likely to have NAFLD than those in the highest quartile in multivariable logistic regression analyses. However, such associations with circulating adipsin were not noted for metabolic syndrome, abnormal liver enzyme and significant liver fibrosis.
These results demonstrate that circulating adipsin levels in Chinese obese adults are negatively associated with risk of NAFLD, implying that serum adipsin levels may be a potential protective factor in NAFLD.
作为一种分泌型脂肪因子,脂肪酶最近被证明在代谢紊乱中起关键作用。然而,关于循环脂肪酶与人类非酒精性脂肪性肝病(NAFLD)关联的信息却很少。
我们从社区招募了1163名肥胖成年受试者,男性腰围至少90厘米,女性腰围至少80厘米。通过酶联免疫吸附测定法测量循环脂肪酶水平。
与非NAFLD受试者相比,NAFLD受试者的循环脂肪酶水平降低(p < 0.05)。血清脂肪酶水平较低的NAFLD患病率显著高于水平较高者(57.6%对50.9%,p < 0.05)。在NAFLD受试者中,循环脂肪酶水平与空腹血糖和餐后血糖水平降低显著相关(交互作用p均< 0.001),而在非NAFLD受试者中则无此关联。在调整年龄、性别、当前吸烟状况、饮酒量、体力活动、BMI、收缩压、空腹血糖、总胆固醇、HDL - c、HOMA - IR和体脂量后,NAFLD风险显著降低21.7% [OR(95%CI):0.783(0.679 - 0.902),p < 0.001]。重要的是,在多变量逻辑回归分析中,循环脂肪酶最低四分位数的受试者患NAFLD的可能性是最高四分位数受试者的1.88倍。然而,未发现循环脂肪酶与代谢综合征、肝酶异常和显著肝纤维化之间存在此类关联。
这些结果表明,中国肥胖成年人的循环脂肪酶水平与NAFLD风险呈负相关,这意味着血清脂肪酶水平可能是NAFLD的潜在保护因素。