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Neutrophil-to-Lymphocyte Ratio as a Cardiovascular Risk Marker May Be Less Efficient in Women Than in Men (CROSBI ID 297770)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Majnarić Ljiljana, Guljaš Silva, Bosnić Zvonimir, Šerić Vatroslav, and Wittlinger Thomas Neutrophil-to-Lymphocyte Ratio as a Cardiovascular Risk Marker May Be Less Efficient in Women Than in Men // Biomolecules, 11 (2021), 4; 527-544. doi: 10.3390/biom11040528

Podaci o odgovornosti

Majnarić Ljiljana, Guljaš Silva, Bosnić Zvonimir, Šerić Vatroslav, and Wittlinger Thomas

engleski

Neutrophil-to-Lymphocyte Ratio as a Cardiovascular Risk Marker May Be Less Efficient in Women Than in Men

Cardiovascular disease (CVD) is the leading cause of death in women, although traditionally, it has been considered as a male dominated disease. Chronic inflammation plays a crucial role in the development of insulin resistance, diabetes type 2 and CVD. Since studies on women were scarce, in order to improve diagnosis and treatment of CVD, there is a need to improve understanding of the role of inflammation in the development of CVD in women. The neutrophil-to-lymphocyte ratio (NLR) is an inexpensive and widely available marker of inflammation, and has been studied in cardio-metabolic disorders. There is a paucity of data on sex specific differences in the lifetime course of NLR. Men and women differ to each other in sex hormones and characteristics of immune reaction and the expression of CVD. These factors can determine NLR values and their variations along the life course. In particular, menopause in women is a period associated with profound physiological and hormonal changes, and is coincidental with aging. An emergence of CV risk factors with aging, and age-related changes in the immune system, are factors that are associated with an increase in prevalence of CVD in both sexes. The aim of this review is to comprehend the available evidence on this issue, and to discuss sex specific differences in the lifetime course of NLR in the light of immune and inflammation mechanisms.

women ; gender ; medicine ; cardiovascular risk ; menopausal transition ; meta inflammation ; bio-mediators

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Podaci o izdanju

11 (4)

2021.

527-544

objavljeno

2218-273X

10.3390/biom11040528

Povezanost rada

Kliničke medicinske znanosti

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