Association of Inflammatory-Hematological Biomarkers with Hypertension and Related Comorbidities

Evelina Maria Gosav1,2, Daniela Maria Tanase1,2, Anca Ouatu1,2

  • 1Department of Internal Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.

Insights

Inflammation markers like neutrophils and lymphocytes are linked to hypertension and its complications, including diabetes and kidney disease. These hematological markers show potential but have limited clinical usability due to low specificity.

Area of Science:

  • Cardiovascular Medicine
  • Nephrology
  • Endocrinology

Background:

  • Arterial hypertension (HTN) is a leading global cause of cardiovascular disease.
  • HTN frequently co-occurs with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD).
  • A pro-inflammatory state often underlies the interconnectedness of HTN, T2DM, and CKD.

Purpose of the Study:

  • To investigate the roles of neutrophils, lymphocytes, and platelets.
  • To evaluate the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR).
  • To assess these markers in patients with HTN, T2DM, and/or CKD.

Main Methods:

  • Retrospective unicentric study of 6077 patients (2018-2023).
  • Comparative multivariate analysis after exclusion criteria application.
  • Statistical analysis including Mann-Whitney U and Kruskal-Wallis tests, and Receiver Operating Characteristic (ROC) analysis.

Main Results:

  • Higher neutrophils, lower lymphocytes, and fluctuating platelets associated with HTN + comorbidities (p < 0.001).
  • ROC analysis indicated significant associations for neutrophils, lymphocytes, NLR, and PLR in various HTN subgroups.
  • AUC specificities were generally below acceptable thresholds, limiting practical clinical utility.

Conclusions:

  • Hematological pro-inflammatory markers are associated with hypertension and its comorbidities.
  • Neutrophils, lymphocytes, NLR, and PLR show potential as indicators in HTN, T2DM, and CKD.
  • Further research is needed to enhance the clinical applicability of these inflammatory markers.

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