Key result
Hypertension linked to markedly higher oxidative stress and inflammation versus healthy controls.
Why the study?
TNF-alpha plays a vital role in the pathogenesis of hypertension and its inhibition improves clinical symptoms, but outcomes on high blood pressure had not been investigated.
Case-Control (n=60)
No
Absolute Event Rate: 5.01% vs 2.12%
p-value: p=<0.0001
Hypertension is associated with increased oxidative stress and inflammation, as evidenced by elevated serum MDA and TNF-α levels and reduced antioxidant capacity (FRAP).
TNF-α was associated with hypertension; leaves open whether inhibition affects blood pressure.
Concurrent with the misbalance of oxidizing agents and antioxidants, high blood pressure is a major physical burden condition in the current scenario. Tumor necrosis factor-α (TNF-α) plays a vital role in the pathogenesis of hypertension. Tumor necrosis factor-α, inhibitor improves clinical symptoms however their outcome on high blood pressure has not been investigated. We investigated the inflammatory marker TNF-α, malondialdehyde (MDA) and ferric reducing antioxidant power (FRAP) in hypertensive patients. We measured randomly blood pressure using an ambulatory observe in hypertensive patients, measured systolic BP X 140 mmHg and/or diastolic BP X 90 mmHg were considered hypertensive. Total 60 cases were considered in the study that involves 30 hypertensive patients and 30 normal control. Measurements of serum concentrations of TNF-α, MDA, FRAP in hypertension patients was done in both the groups. Serum TNF-α was found to be remarkably increased in study subjects as compared to normal group (r=0.32, p<0.0001*). Serum MDA was also raised in hypertensive as compared to control (r=0.99**, p<0.0001*). While Serum FRAP was found to be decreased in hypertensive group in comparison to healthy control (r=0.23, p<0.0001*). It is concluded that high blood pressure leads to generation of oxidative stress with remarkable elevation of TNF-α and malondialdehyde levels. While reduced FRAP indicates its probable role in lipid peroxidation and in the pathogenesis of hypertension.
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Verma et al. (2019) conducted a case-control in Hypertension (n=60). Hypertension vs. Normotensive controls was evaluated on Serum TNF-α (ng/mL) (p=<0.0001). Hypertension was associated with significantly elevated oxidative stress and inflammation, demonstrated by higher serum TNF-α (5.01 vs 2.12 ng/mL) and MDA (4.77 vs 1.89 µmol/L), alongside reduced FRAP compared to healthy controls.
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