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DOI 10.20945/2359-3997000000298

Медицинская библиотека · Archives of endocrinology and metabolism · 2020

Uric acid as a predictor of endothelial dysfunction in patients with metabolic syndrome.

Singh Charanpreet, Jain Sanjay, Dhawan Veena, Kalra Naveen, Kumari Savita

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Аннотация

OBJECTIVE

We conducted a study to examine the association of endothelial dysfunction and oxidative stress with uric acid levels in patients of metabolic syndrome.

METHODS

One hundred and two patients of Metabolic Syndrome (International Diabetes Federation definition) were included in the study. Anthropometric measurements, serum uric acid levels, fasting blood sugar levels and lipid levels, as well as malondialdehyde and reactive nitrogen intermediates were measured after an 8-hour fasting period. Flow mediated vasodilation (FMD) of the brachial artery was measured and endothelial dysfunction was defined as an increase in diameter < 10% post compression.

RESULTS

A total of 102 patients were included in the study. Mean uric acid level was 5.49 ± 1.61 mg%. A total of 59 patients in the study had endothelial dysfunction, defined by an abnormal FMD. Patients with an abnormal FMD had higher levels of serum uric acid which was statistically significant (p value = 0.010). Serum RNI and MDA levels were negatively correlated with uric acid, but did not reach statistical significance. Patients with an abnormal FMD had a lower RNI level, but this did not reach statistical significance. Serum MDA levels were significantly higher in patients with an abnormal FMD (p value = 0.038).

CONCLUSION

Uric acid was significantly associated with endothelial dysfunction in patients with metabolic syndrome in our study. It was inversely correlated with serum RNI and MDA levels, but this did not reach statistical significance.

Для цитирования: Singh Charanpreet, Jain Sanjay, Dhawan Veena, Kalra Naveen, Kumari Savita. Uric acid as a predictor of endothelial dysfunction in patients with metabolic syndrome.. Archives of endocrinology and metabolism. 2020. DOI: 10.20945/2359-3997000000298.

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