Fibrosis markers, hip fracture risk, and bone density in older adults

• Type of Material: Article
• Authors: Joshua Barzilay, Emory University; Petra Buzkova, University of Washington; Jorge R. Kizer, Albert Einstein College of Medicine; Luc Djousse, Brigham & Womens Hospital; Joachim H. Ix, University of California San Diego; Howard A. Fink, Veterans Affairs Medical Center; David S. Siscovick, New York Academy of Science; Jane A. Cauley, University of Pittsburgh; Kenneth J. Mukamal, Beth Israel Deaconess Medical Center
• Language: English
• Date: 2016-02-01
• Publisher: Springer London
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2015, International Osteoporosis Foundation and National Osteoporosis Foundation.
• Final Published Version (URL): http://dx.doi.org/10.1007/s00198-015-3269-9
• Title of Journal or Parent Work: Osteoporosis International
• Volume: 27
• Issue: 2
• Start Page: 815
• End Page: 820
• Grant/Funding Information: This work was also funded in part by R01 HL094555 from the National Heart, Lung, and Blood Institute (to Drs. Djoussé, Ix, Kizer, and Mukamal).; This research was supported by contracts HHSN268201200036C, HHSN268200800007C, N01 HC55222, N01HC85079, N01HC85080, N01HC85081, N01HC85082, N01HC85083, N01HC85086, and grant HL080295 from the National Heart, Lung, and Blood Institute (NHLBI), with additional contribution from the National Institute of Neurological Disorders and Stroke (NINDS).
• Keywords: EXPRESSION; Endocrinology & Metabolism; Bone mineral density; Hip fracture; Life Sciences & Biomedicine; DIFFERENTIATION; TGF-BETA; PIIINP; Science & Technology; DISEASE; BIOMARKERS; GROWTH-FACTOR-BETA; TGF-beta
• Research Categories: Health Sciences, Medicine and Surgery; Biology, Anatomy

Abstract

Summary: We examined whether blood levels of two markers of fibrosis (transforming growth factor beta one (TGF-β1) and procollagen type III N-terminal propeptide (PIIINP)) are related to hip fracture risk and to bone mineral density (BMD). TGF-β1 levels were associated with lower hip fracture risk in women and with lower BMD in men. PIIINP levels were not associated with either outcome. Introduction: TGF-β1 serves several roles in bone formation and resorption. A consequence of TGF-β1 activation is the production of PIIINP, a marker of collagen III deposition. Here, we explore whether these two biomarkers are related to incident hip fracture and bone mineral density (BMD) and whether their associations are modified by systemic inflammation, as measured by C-reactive protein (CRP) levels. Methods: Participants were from the Cardiovascular Health Study (mean age 78 years; mean follow-up 8.3 years). We included 1681 persons with measured levels of TGF-β1 (149 hip fractures) and 3226 persons with measured levels of PIIINP (310 hip fractures). Results: Among women, higher TGF-β1 levels were associated with lower hip fracture risk (HR, per doubling, 0.78 [95 % CI 0.61, 0.91]). Among men, TGF-β1 levels were associated with hip fracture risk in a non-linear manner, but among those with elevated CRP levels, doubling was associated with increased risk of fracture (HR 2.22 [1.20, 4.08]) (p = 0.02, interaction between low and high CRP and TGF-β1 on fracture risk). TGF-β1 levels had no significant association with total hip or total body BMD in women but were significantly associated with lower BMD in men. There were no associations of PIIINP levels with hip fracture risk or BMD in men or women. Conclusions: TGF-β1 levels appear to be associated with bone-related phenotypes in a sex-specific manner. The reasons for these differences between men and women regarding TGF-β1 levels and hip fracture risk and bone density require further investigation.