Tonelli Adriano R, Fares Wassim H, Dakkak Wael, Rao Youlan, Zhou Xuan, Dweik Raed A
1 Department of Pulmonary, Allergy and Critical Care Medicine, Respiratory Institute, Cleveland Clinic, Cleveland, OH, USA.
2 Section of Pulmonary, Critical Care & Sleep Medicine, Department of Internal Medicine, Yale University, New Haven, CT, USA.
Pulm Circ. 2017 Jul-Sep;7(3):727-729. doi: 10.1177/2045893217717219. Epub 2017 Jun 27.
Leptin (a neuroendocrine peptide that enhances metabolism and acts on the hypothalamus to suppress appetite) and adiponectin (a protein that has insulin-sensitizing, anti-inflammatory, and antiproliferative properties) are involved in the pathobiology of pulmonary arterial hypertension (PAH). We hypothesized that plasma leptin and adiponectin as well as the leptin/adiponectin ratio are abnormal in PAH patients and their levels track with disease severity and functional changes during follow-up. We tested this hypothesis in a cohort of patients included in the 16-week, international, multicenter, double-blind, placebo-controlled FREEDOM-C2 study. Blood was collected at baseline and week 16 in 178 out of 310 randomized patients with PAH. Baseline plasma leptin and adiponectin concentrations were 25 ± 31 ng/mL and 7.8 ± 6.1 ug/mL, respectively. Leptin, adiponectin, and leptin/adiponectin (mean ± SD) changes at 16 week were of small magnitude. Leptin at baseline was significantly associated with older age, higher BMI, higher Borg dyspnea index, and lower NT-pro BNP. Women had higher levels of leptin than men (30.5 ± 33.2 versus 7.2 ± 6.4 ng/mL), even when adjusting for background therapy and etiology (linear regression: β = 21.8, P < 0.001). Adiponectin was negatively associated with BMI and positively associated with NT-pro BNP. Changes in leptin, adiponectin, and leptin/adiponectin ratio adjusted for weight at 16 weeks did not predict functional class, distance walk in 6 min or survival at one, two, three, or four years. Plasma leptin and adiponectin at baseline and their change at 16-week do not appear to significantly impact prognosis in PAH.
瘦素(一种增强新陈代谢并作用于下丘脑以抑制食欲的神经内分泌肽)和脂联素(一种具有胰岛素增敏、抗炎和抗增殖特性的蛋白质)参与了肺动脉高压(PAH)的病理生物学过程。我们假设PAH患者的血浆瘦素和脂联素以及瘦素/脂联素比值异常,且它们的水平在随访期间与疾病严重程度和功能变化相关。我们在纳入16周国际多中心双盲安慰剂对照FREEDOM - C2研究的一组患者中验证了这一假设。在310例随机分组的PAH患者中,178例在基线和第16周时采集了血液样本。基线时血浆瘦素和脂联素浓度分别为25±31 ng/mL和7.8±6.1 μg/mL。第16周时瘦素、脂联素和瘦素/脂联素(均值±标准差)的变化幅度较小。基线时瘦素与年龄较大、体重指数较高、博格呼吸困难指数较高以及N末端脑钠肽前体(NT - pro BNP)较低显著相关。即使在调整背景治疗和病因后,女性的瘦素水平仍高于男性(30.5±33.2与7.2±6.4 ng/mL)(线性回归:β = 21.8,P < 0.001)。脂联素与体重指数呈负相关且与NT - pro BNP呈正相关。在第16周时,调整体重后瘦素、脂联素和瘦素/脂联素比值的变化并不能预测功能分级、6分钟步行距离或1年、2年、3年或4年的生存率。PAH患者基线时的血浆瘦素和脂联素及其在第16周时的变化似乎对预后没有显著影响。