Relationship between oxidative stress parameters and asymptomatic organ damage in hypertensive patients without diabetes mellitus

被引:18
作者
Ates, Ihsan [1 ]
Ozkayar, Nihal [2 ]
Topcuoglu, Canan [3 ]
Dede, Fatih [2 ]
机构
[1] Ankara Numune Training & Res Hosp, Dept Internal Med, TR-06100 Ankara, Turkey
[2] Ankara Numune Training & Res Hosp, Dept Nephrol, TR-06100 Ankara, Turkey
[3] Ankara Numune Training & Res Hosp, Dept Biochem, Ankara, Turkey
关键词
asymptomatic organ damage; hypertension; oxidative stres; total antioxidant status; total oxidant status; INTIMA-MEDIA THICKNESS; REACTIVE OXYGEN; PATHOPHYSIOLOGY; PARAOXONASE; HYPERTROPHY; EXPRESSION; MARKERS;
D O I
10.3109/14017431.2015.1060355
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. We aimed to evaluate the levels of oxidative stress (OS) parameters such as total antioxidant status or TAS, total oxidant status (TOS), OS index (OSI), paraoxonase 1 (PON1), arylesterase, and total thiol in hypertensive patients with and without asymptomatic organ damage (AOD), and to determine the relationship between these parameters and AOD. Design. Sixty-six patients (21 men, 45 women) with AOD and 66 patients without AOD (21 men, 45 women) were enrolled in the study. Serum OS parameters were measured by colorimetric method. Results. The OSI levels were found to be higher while PON1, PON1/high-density lipoprotein, and arylesterase levels were found to be lower in patients with AOD compared with those in the patients without AOD. Stepwise regression analysis showed high 24-h mean systolic blood pressure, OSI, and low arylesterase level to be independent predictors of AOD. Conclusion. OS level was found to be higher in hypertensive patients with AOD compared with the patients without AOD. However, it is not clear whether increased OS leads to AOD or AOD increases the level of OS. For this purpose, OS level needs to be decreased by antioxidant therapies and patients need to be followed up for a longer duration.
引用
收藏
页码:249 / 256
页数:8
相关论文
共 26 条
[1]   Reactive oxygen species in mechanical stress-induced cardiac hypertrophy [J].
Aikawa, R ;
Nagai, T ;
Tanaka, M ;
Zou, YZ ;
Ishihara, T ;
Takano, H ;
Hasegawa, H ;
Akazawa, H ;
Mizukami, M ;
Nagai, R ;
Komuro, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 289 (04) :901-907
[2]   The relationship between asymptomatic organ damage, and serum soluble tumor necrosis factor-like weak inducer of apoptosis (sTWEAK) and Interleukin-17A (IL-17A) levels in non-diabetic hypertensive patients [J].
Ates, Ihsan ;
Ozkayar, Nihal ;
Akyel, Fatma ;
Topcuoglu, Canan ;
Akyel, Serdar ;
Barca, A. Nurdan ;
Dede, Fatih .
BMC NEPHROLOGY, 2014, 15
[3]  
Cao Jie, 2013, Zhonghua Xin Xue Guan Bing Za Zhi, V41, P857
[4]   Expression and cellular localization of classic NADPH oxidase subunits in the spontaneously hypertensive rat kidney [J].
Chabrashvili, T ;
Tojo, A ;
Onozato, ML ;
Kitiyakara, C ;
Quinn, MT ;
Fujita, T ;
Welch, WJ ;
Wilcox, CS .
HYPERTENSION, 2002, 39 (02) :269-274
[5]   ECHOCARDIOGRAPHIC DETERMINATION OF LEFT-VENTRICULAR MASS IN MAN - ANATOMIC VALIDATION OF METHOD [J].
DEVEREUX, RB ;
REICHEK, N .
CIRCULATION, 1977, 55 (04) :613-618
[6]  
Digiesi V, 1997, Clin Ter, V148, P515
[7]   The chemistry of cell signaling by reactive oxygen and nitrogen species and 4-hydroxynonenal [J].
Forman, Henry Jay ;
Fukuto, Jon M. ;
Miller, Tom ;
Zhang, Hongqiao ;
Rinna, Alessandra ;
Levy, Smadar .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2008, 477 (02) :183-195
[8]   Essential hypertension and oxidative stress: New insights [J].
Gonzalez, Jaime ;
Valls, Nicolas ;
Brito, Roberto ;
Rodrigo, Ramon .
WORLD JOURNAL OF CARDIOLOGY, 2014, 6 (06) :353-366
[9]  
Hadi HAR, 2005, VASC HEALTH RISK MAN, V1, P183
[10]  
Hendre Anup S, 2013, J Indian Med Assoc, V111, P377