Endocrinology and Diabetes Center, Yokohama Rosai Hospital, Yokohama, Kanagawa, Japan.
PLoS One. 2018 May 1;13(5):e0196526. doi: 10.1371/journal.pone.0196526. eCollection 2018.
Pentraxin 3 (PTX3) is reported to be a vascular inflammation marker providing prognostic information of vasculopathy. Until today, however, the effect of aldosterone or oxidative stress on the regulation of PTX3 is unknown. In present study, we investigated to find regulative factors, especially aldosterone and oxidative stress, on PTX3. Serum PTX3 levels were measured in 75 patients (45 male and 30 women, aged 55.1±13.4 year-old (mean±SD)) with various endocrine disorders including 47 with diabetes, 24 with primary aldosteronism (PA). All participants were free from cardio vascular diseases and diabetic retinopathy. Serum PTX3 level was significantly lower in patients with PA than without PA and was significantly higher in patients with diabetes than without diabetes. PTX3 was significantly correlated with glycated hemoglobin (HbA1c), urinary albumin excretion (UAE) and plasma aldosterone concentration (PAC) (r = 0.431, P<0.001; r = 0.313, P = 0.009; r = -0.375, P = 0.004). A stepwise multiple regression analysis chose HbA1c and UAE as independent determinants of PTX3 (β = 0.282, P<0.001; β = 0.783, P<0.001). On the other hand, PTX3 was not significantly correlated with HbA1c and UAE but significantly negatively correlated with PAC in patients with diabetes. Therefore, it might be suggested that PTX3 is positively regulated by chronic hyperglycemia but negatively regulated by aldosterone, and is associated with urinary albumin excretion as a micro vasculopathy.
血清 pentraxin 3(PTX3)被报道为一种血管炎症标志物,可提供血管病变的预后信息。然而,到目前为止,醛固酮或氧化应激对 PTX3 调节的影响尚不清楚。在本研究中,我们研究了寻找调节因子,特别是醛固酮和氧化应激对 PTX3 的调节作用。在 75 例患有各种内分泌疾病的患者(45 名男性和 30 名女性,年龄 55.1±13.4 岁(平均值±标准差))中测量了血清 PTX3 水平,其中包括 47 例糖尿病患者,24 例原发性醛固酮增多症(PA)患者。所有参与者均无心血管疾病和糖尿病性视网膜病变。PA 患者的血清 PTX3 水平明显低于无 PA 患者,而糖尿病患者的血清 PTX3 水平明显高于无糖尿病患者。PTX3 与糖化血红蛋白(HbA1c)、尿白蛋白排泄率(UAE)和血浆醛固酮浓度(PAC)显著相关(r = 0.431,P<0.001;r = 0.313,P = 0.009;r = -0.375,P = 0.004)。逐步多元回归分析选择 HbA1c 和 UAE 作为 PTX3 的独立决定因素(β = 0.282,P<0.001;β = 0.783,P<0.001)。另一方面,在糖尿病患者中,PTX3 与 HbA1c 和 UAE 无显著相关性,但与 PAC 呈显著负相关。因此,PTX3 可能是由慢性高血糖正向调节,由醛固酮负向调节,与尿白蛋白排泄有关,作为一种微血管病变。