Increased systemic inflammation and altered distribution of T-cell subsets in postmenopausal women

PLoS One. 2020 Jun 23;15(6):e0235174. doi: 10.1371/journal.pone.0235174. eCollection 2020.

Abstract

Aim: To investigate markers of systemic inflammation in pre- and postmenopausal women and identify possible predictors of systemic inflammation with menopause.

Methods: Cross-sectional study of 69 healthy women between 45- and 60 years. Blood samples were collected to assess leukocyte subsets and plasma cytokines. MRI and DXA scans were performed to assess body composition. Through uni- and multivariate analyses, follicle-stimulating hormone (FSH), visceral fat mass and age were evaluated as predictors of systemic inflammation in relation to menopause.

Results: Postmenopausal women tended to have higher leukocyte counts (5.4 x109 vs. 4.9 x109 cells/l, p = 0.05) reflected in increased total lymphocytes (1.8 x109 vs. 1.6 x109 cells/l, p = 0.01) and monocytes (0.5 x109 vs. 0.4 x109 cells/l, p = 0.02), compared to premenopausal women. Increased visceral fat mass was a strong predictor of high leukocyte subsets. Postmenopausal women had higher plasma TNF-α (2.24 vs. 1.91 pg/ml, p = 0.01) and IL-6 (0.45 vs. 0.33 pg/ml, p = 0.004) compared to premenopausal women and high FSH was a significant predictor of increased plasma TNF-α, IL-1β and IL-6. Menopause was further associated with increased T-cells (1,336 vs. 1,128 cells/μl, p = 0.04) reflected in significantly higher counts of exhausted-, senescent-, and memory CD4+ T-cell subsets.

Conclusions: Menopause is associated with increased systemic inflammation as well as exhausted- and senescent T-cells. We suggest, that both increased visceral fat mass and declining sex hormone levels might contribute to postmenopausal systemic inflammation and calls for further large-scale studies to confirm these findings.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorptiometry, Photon / methods
  • Body Composition
  • Cytokines / blood
  • Cytokines / immunology*
  • Cytokines / metabolism
  • Female
  • Follicle Stimulating Hormone / blood
  • Follicle Stimulating Hormone / immunology
  • Gonadal Steroid Hormones / blood
  • Gonadal Steroid Hormones / immunology
  • Humans
  • Inflammation / blood
  • Inflammation / immunology*
  • Inflammation / metabolism
  • Intra-Abdominal Fat / diagnostic imaging
  • Intra-Abdominal Fat / immunology
  • Intra-Abdominal Fat / metabolism
  • Lymphocytes / cytology
  • Lymphocytes / immunology
  • Lymphocytes / metabolism
  • Magnetic Resonance Imaging / methods
  • Middle Aged
  • Monocytes / cytology
  • Monocytes / immunology
  • Monocytes / metabolism
  • Multivariate Analysis
  • Postmenopause / blood
  • Postmenopause / immunology*
  • Postmenopause / metabolism
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism

Substances

  • Cytokines
  • Gonadal Steroid Hormones
  • Follicle Stimulating Hormone

Grants and funding

The Centre for Physical Activity Research (CFAS) is supported by TrygFonden (grants ID 101390 and ID 20045). During the study period, the Centre of Inflammation and Metabolism (CIM) was supported by a grant from the Danish National Research Foundation (DNRF55). The funding sources were not involved in the conduction of the study or interpretation of the results.