Detection of kidney dysfunction potential biomarkers with hypertension in the persons of 25–45 years

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Abstract

Aim. To assess the significance of symmetrical dimethylarginine (SDMA), uromodulin, retinol-binding protein 4 (RSB-4), transforming growth factor b1 (TGF-b1), plasminogen activator inhibitor 1 (PAI-1) as kidney dysfunction potential biomarkers persons with hypertension in persons 25–45 years old.

Materials and methods. The study included 147 people. Hypertension was recorded with blood pressure (BP)≥140/90 mm Hg, renal dysfunction – with GFRCKD-EPI<90 ml/min/1.73 cm2. Four groups were formed: 1 – individuals with hypertension and GFR<90 ml/min/1.73 cm2; 2 – with hypertension and GFR≥90 ml/min/1.73 cm2; 3 – with BP<140/90 mm Hg and GFR<90 ml/min/1.73 cm2; 4 – with BP<140/90 mm Hg and GFR≥90 ml/min/1.73 cm2. The groups were comparable by gender, age, and number of respondents. Creatinine, SDMA, uromodulin, RSB-4, TGF-b1, PAI-1 levels were examined in all individuals in the serum.

Results. The maximum values of SDMA were determined in the 1st and 3rd groups (1.30 and 1.36 μmol/l). In the 1st group, an association was found between SDMA and GFR (r=-0.324; p=0.048). In the 1st group, the minimum values of uromodulin were recorded, in the 4th group – the maximum values (164.86 and 188.90 ng/ml; at the same time р=0.921). The level of RSB-4 was the highest in the 1st group, the lowest – in the 4th group (88.64 and 80.05 µg/ml; p=0.011). The association of RSB-4 with SDMA in the 3rd group (r=0.400; p=0.017), the 4th group (r=0.403; p=0.018) was detected. The level of TGF-b1 was 1.5 times higher in the 1st group than in the 3rd (23.16 and 15.99 µg/ml; p=0.026), the association of TGF-b1 with GFR in the 1st group had the opposite direction (r=-0.452; p=0.005). The study of similar indicators of PAI-1 did not reveal its relationship with renal dysfunction in hypertension.

Conclusion. The results of the study made it possible to consider SDMA, RSB-4, TGF-b1 as potential biomarkers of renal dysfunction in hypertension in persons 25–45 years old.

About the authors

N. A. Kovalkova

Research Institute of Internal and Preventive Medicine – branch of the Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences

Author for correspondence.
Email: terap2000@yandex.ru
ORCID iD: 0000-0001-5368-1899

к.м.н., ст. науч. сотр.

Russian Federation, Novosibirsk

A. D. Khudyakova

Research Institute of Internal and Preventive Medicine – branch of the Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences

Email: terap2000@yandex.ru
ORCID iD: 0000-0001-5397-0498

аспирант

Russian Federation, Novosibirsk

E. V. Kashtanova

Research Institute of Internal and Preventive Medicine – branch of the Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences

Email: terap2000@yandex.ru
ORCID iD: 0000-0003-2268-4186

д.б.н., ст. науч. сотр.

Russian Federation, Novosibirsk

Ya. V. Polonskaya

Research Institute of Internal and Preventive Medicine – branch of the Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences

Email: terap2000@yandex.ru
ORCID iD: 0000-0002-3538-0280

д.б.н., ст. науч. сотр.

Russian Federation, Novosibirsk

L. V. Shcherbakova

Research Institute of Internal and Preventive Medicine – branch of the Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences

Email: terap2000@yandex.ru
ORCID iD: 0000-0001-9270-9188

ст. науч. сотр.

Russian Federation, Novosibirsk

Yu. I. Ragino

Research Institute of Internal and Preventive Medicine – branch of the Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences

Email: terap2000@yandex.ru
ORCID iD: 0000-0002-4936-8362

чл.-кор. РАН, д.м.н., врио руководителя

Russian Federation, Novosibirsk

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