Bone Density Loss Is Associated With Blood Cell Counts
نویسنده :
تاریخ انتشار : 1396/03/29
Hematopoiesis depends on a supportive microenvironment. Preclinical studies in mice have demonstrated that osteoblasts
influence the development of blood cells, particularly erythrocytes, B lymphocytes, and neutrophils. However, it is unknown whether
osteoblast numbers or function impact blood cell counts in humans. We tested the hypothesis that men with low BMD or greater
BMD loss have decreased circulating erythrocytes and lymphocytes and increased myeloid cells. We performed a cross-sectional
analysis and prospective analysis in the Osteoporotic Fractures in Men (MrOS) study, a multisite longitudinal cohort study. A total of
2571 community-dwelling men (65 years) who were able to walk without assistance, did not have a hip replacement or fracture,
and had complete blood counts (CBCs) at the third study visit were analyzed. Multivariable (MV)-adjusted logistic regression
estimated odds of white blood cell (WBC) subtypes (highest and lowest quintile versus middle), and anemia (clinically defined)
associated with BMD by DXA scan (at visit 3), annualized percent BMD change (baseline to visit 3), and high BMD loss (>0.5%/year,
from baseline to visit 3) at the femoral neck (FN) and total hip (TH). MV-adjusted models included age, BMI, cancer history, smoking
status, alcohol intake, corticosteroid use, self-reported health, thiazide use, and physical activity. At visit 3 greater TH BMD loss (per 1
SD) was associated with increased odds of anemia, high neutrophils, and low lymphocytes. Annualized BMD loss of >0.5% was
associated with increased odds of anemia, high neutrophils, and low lymphocytes. Similar results were observed for FN BM
regarding anemia and lymphocytes. We conclude that community-dwelling older men with declining hip BMD over about 7 years
had increased risks of anemia, lower lymphocyte count, and higher neutrophil count, consistent with preclinical studies. Bone
health and hematopoiesis may have greater interdependency than previously recognized. © 2016 American Society for Bone and
Mineral Research.