Department of Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Free Radic Biol Med. 2022 Jul;187:123-131. doi: 10.1016/j.freeradbiomed.2022.05.020. Epub 2022 May 28.
Oxidative stress is known to be involved in the development of hypertension, but accurate redox biomarkers predicting the risk of developing hypertension are scarce. Serum free sulfhydryl groups (R-SH, free thiols) have been shown to accurately reflect systemic oxidative stress in various conditions. In this study, we aimed to investigate associations between serum free thiols and the risk of developing new-onset hypertension in a population-based cohort study.
Subjects (n = 3,575) who participated in the Prevention of REnal and Vascular ENd-stage Disease (PREVEND) study, a prospective, population-based cohort study in the Netherlands, were included. Baseline protein-adjusted serum free thiols were studied for their associations with the development of hypertension, defined as a systolic blood pressure (SBP) of at least 140 mmHg, a diastolic blood pressure (DBP) of at least 90 mmHg, or the first usage of antihypertensive medication. Subjects with hypertension at baseline were excluded from the study.
Mean protein-adjusted serum free thiols at baseline was 5.16 μmol/g of protein (range: 1.62-8.41 μmol/g). Protein-adjusted serum free thiols were significantly associated with the risk of incident hypertension (hazard ratio [HR] per doubling 0.60 [95% confidence interval [CI]: 0.49-0.72, P < 0.001), also after adjustment for age and sex (HR 0.81 [95% CI: 0.66-0.91], P < 0.05), but not after additional adjustment for relevant confounding factors (HR 0.90 [95% CI: 0.70-1.15], P = 0.382).
Higher levels of serum free thiols, i.e. less oxidative stress, are associated with a decreased risk of developing incident hypertension in subjects from the general population.
氧化应激被认为与高血压的发生有关,但准确预测高血压发生风险的氧化还原生物标志物却很少。血清游离巯基(R-SH,游离硫醇)已被证明可在各种情况下准确反映全身氧化应激。在这项研究中,我们旨在研究人群基础队列研究中血清游离巯基与新发高血压风险之间的关系。
本研究纳入了参加预防肾脏和血管终末期疾病(PREVEND)研究的受试者(n=3575),这是一项在荷兰进行的前瞻性人群基础队列研究。研究了基线时经蛋白校正的血清游离巯基与高血压发展之间的关系,高血压定义为收缩压(SBP)至少 140mmHg、舒张压(DBP)至少 90mmHg 或首次使用抗高血压药物。排除基线时患有高血压的受试者。
基线时经蛋白校正的血清游离巯基平均值为 5.16μmol/g 蛋白(范围:1.62-8.41μmol/g)。经蛋白校正的血清游离巯基与新发高血压的风险显著相关(每翻倍的风险比[HR]为 0.60[95%置信区间[CI]:0.49-0.72,P<0.001]),调整年龄和性别后也是如此(HR 0.81[95% CI:0.66-0.91],P<0.05),但在进一步调整相关混杂因素后则不然(HR 0.90[95% CI:0.70-1.15],P=0.382)。
来自一般人群的血清游离巯基水平较高,即氧化应激程度较低,与新发高血压的发生风险降低相关。