Ma Fei, Hao Jing, Zhao Jing, Liu De-Ying, Cao Hui-Li, Yang Bing, Li Jin
Department of Neurology, Shan Xi Children Hospital, China.
Department of Physiology, Shan Xi Medical University, China.
Int J Cardiol. 2022 May 1;354:50-55. doi: 10.1016/j.ijcard.2022.03.011. Epub 2022 Mar 10.
Family with sequence similarity 19 member A5 (FAM19A5) has been identified as a novel adipokine that plays an important role in inhibiting inflammation and vascular smooth muscle cell proliferation. However, the clinical associations between FAM19A5 levels and the presence and severity of coronary artery disease (CAD) remains uncertain.
We measured serum FAM19A5 levels in 186 CAD patients and 58 non-CAD patients who underwent coronary arteriography (CAG) recruited in Shanxi Medical University Affiliated Second Hospital. The severity of coronary artery stenosis was represented in the Gensini score. Logistic and linear regression analyses were used to analyze the relationship between serum FAM19A5 and CAD.
Serum FAM19A5 levels in CAD group were significantly lower than those in the non-CAD group [1.53 (1.13-2.27) ng/mL vs 2.33 (1.69-3.51) ng/mL; P = 0.013]. Logistic regression analysis showed that decreased serum FAM19A5 level was a risk factor for CAD (OR: 0.563, 95% CI: 0.409-0.776, P < 0.001). Circulating FAM19A5 levels were negatively associated with the Gensini score. FAM19A5 had 87.9% sensitivity and 52.7% specificity for identifying CAD.
Serum FAM19A5 levels were negatively associated with the presence and severity of CAD and may represent a novel biomarker for diagnosing and indication the severity of CAD.
序列相似性家族19成员A5(FAM19A5)已被鉴定为一种新型脂肪因子,在抑制炎症和血管平滑肌细胞增殖中起重要作用。然而,FAM19A5水平与冠状动脉疾病(CAD)的存在及严重程度之间的临床关联仍不确定。
我们检测了山西医科大学附属第二医院招募的186例CAD患者和58例接受冠状动脉造影(CAG)的非CAD患者的血清FAM19A5水平。冠状动脉狭窄的严重程度用Gensini评分表示。采用逻辑回归和线性回归分析来分析血清FAM19A5与CAD之间的关系。
CAD组血清FAM19A5水平显著低于非CAD组[1.53(1.13 - 2.27)ng/mL对2.33(1.69 - 3.51)ng/mL;P = 0.013]。逻辑回归分析显示,血清FAM19A5水平降低是CAD的一个危险因素(OR:0.563,95%CI:0.409 - 0.776,P < 0.001)。循环FAM19A5水平与Gensini评分呈负相关。FAM19A5在识别CAD方面具有87.9%的敏感性和52.7%的特异性。
血清FAM19A5水平与CAD的存在及严重程度呈负相关,可能代表一种用于诊断和指示CAD严重程度的新型生物标志物。