Effects of valsartan on inflammatory and oxidative stress markers in hypertensive, hyperglycemic patients: An open-label, prospective study

被引:6
|
作者
Kuboki, Koji [1 ]
Iso, Kaoru
Murakami, Eiichi
Abe, Seiko
Araki, Emi
Ueshiba, Hajime
Yoshino, Gen
机构
[1] Toho Univ, Sch Med, Dept Internal Med, Div Endocrinol Diabet & Metab, Tokyo, Japan
[2] Toho Univ, Omori Hosp, Sch Med, Clin Lab, Tokyo, Japan
[3] Mitsubishi Bio Clin Labs Inc, Testing Dept D, Tokyo, Japan
来源
CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL | 2007年 / 68卷 / 05期
关键词
valsartan; hypertension; diabetes; inflammatory marker; oxidative stress marker;
D O I
10.1016/j.curtheres.2007.10.008
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Diabetes mellitus and hypertension are aggravated by activation of the renin-angiotensin system caused by increased oxygen stress and local inflammatory responses. Several studies have suggested that angiotensin 11 type 1 receptors can reduce inflammatory markers (high-sensitivity C-reactive protein [hs-CRP], interleukin [IL]-6, IL-18, soluble vascular cell adhesion molecule [VCAM]-1, and L-selectin) and oxidative stress markers (urinary 8-hydroxy-7,8-dihydro-2'-deoxyguanosine [8-OHdG] and 8-epi-prostaglandin F2(alpha)[8-isoprostane]) in hypertensive patients. Objective: The aim of this study was to assess the effects of valsartan, an angiotensin 11 receptor blocker, on inflammatory and oxidative stress markers in hypertensive patients with mild diabetes or impaired glucose tolerance. Methods: In this open-label, prospective study, hypertensive patients aged > 20 years with mild diabetes (requiring treatment by diet alone or an oral hypoglycemic), seen on an outpatient basis at the Division of Diabetes, Metabolism, and Endocrinology, Omori Hospital, Toyko, Japan, who were receiving a therapeutic dietary regimen for >= l month in the treatment of diabetes or hypertension, were eligible for enrollment. Blood pressure, inflammatory markers (hs-CRP, IL-6, IL-18, VCAM-1, and L-selectin), and oxidative stress markers (urinary 8-OHdG and 8-isoprostane) were monitored before treatment commencement with valsartan (40-80 mg/d) and after 3 months of treatment. Results: A total of 26 patients (18 men, 8 women; mean [SD] age, 57.7 [11.3] years; mean [SD] weight, 65.3 [13.1] kg) were enrolled in the study. After 3 months of treatment, patients' mean (SD) blood pressure had significantly decreased from 153.1 (11.2)/88.3 (11.4) to 143.7 (13.7)/85.2 (9.0) mm Hg (P < 0.05). Among the inflammatory and oxidative stress markers, hs-CRP, VCAM-1, and urinary 8-OHdG concentrations decreased significantly from 0.231 (0.199) to 0.134 (0.111) mg/dL (P= 0.043), 471.1 (193.9) to 403.2 (135.2) ng/mL (P= 0.012), and 12.12 (5.99) to 8.07 (3.36) ng/mg - creatinine (P = 0.001), respectively. The reductions in these markers were observed in patients regardless of whether or not their glycosylated hemoglobin (HbAj) concentration improved (defined as a decrease of >= 1% in HbA(1c)) Conclusion: This small, open-label, prospective study found that a 3-month treatment with valsartan was associated with a significant reduction of hs-CRP, VCAM-I, and urinary 8-OHdG concentrations independent of improvement in HbA(1c) concentration in these hypertensive patients with hyperglycernia.
引用
收藏
页码:338 / 348
页数:11
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