Document Detail


Sclerostin is positively associated with bone mineral density in men and women and negatively associated with carotid calcified atherosclerotic plaque in men from the African American-Diabetes Heart Study.
MedLine Citation:
PMID:  24178795     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONTEXT: Bone mineral density (BMD) and calcified atherosclerotic plaque (CP) demonstrate inverse relationships. Sclerostin, an endogenous regulator of the Wnt pathway and bone formation, has been associated with impaired osteoblast activation and may play a role in vascular calcification.
OBJECTIVE: Our objective was to assess the relationships between sclerostin, BMD, and CP.
DESIGN: Generalized linear models were fitted to test for associations between sclerostin, volumetric BMD (vBMD), and CP.
PARTICIPANTS: A targeted population of 450 unrelated African Americans (AAs) with type 2 diabetes (T2D) was 56% female with mean/SD/median age of 55.4/9.5/55.0 years and a diabetes duration of 10.3/8.2/8.0 years.
MAIN OUTCOME MEASURES: Plasma sclerostin, computed tomography-derived thoracic and lumbar vertebrae trabecular vBMD, coronary artery, carotid artery, and aortoiliac CP were measured.
RESULTS: Plasma sclerostin was 1119/401/1040 pg/mL, thoracic vBMD was 206.3/52.4/204.8 mg/cm3, lumbar vBMD was 180.7/47.0/179.0 mg/cm3, coronary artery CP score was 284/648/13, carotid artery CP score was 46/132/0, and aortoiliac CP score was 1613/2910/282. Sclerostin levels were higher in men than women (P<.0001). Before and after adjusting for age, sex, body mass index, blood pressure, smoking, hemoglobin A1c, and low-density lipoprotein-cholesterol, plasma sclerostin levels were positively associated with thoracic and lumbar vertebrae vBMD (P<.0001). Sex-stratified analyses verified significant relationships in both men and women (both P<.001). Sclerostin was not associated with CP except for an inverse relationship with carotid CP in men (fully adjusted model, P=.03).
CONCLUSIONS: In this cross-sectional study of AA men and women with T2D, circulating sclerostin was positively associated with vBMD in the spine in both sexes and inversely associated with carotid artery CP in men. Sclerostin may play a role in skeletal mineral metabolism in AA but fails to explain inverse relationships between BMD and CP.
Authors:
Thomas C Register; Keith A Hruska; Jasmin Divers; Donald W Bowden; Nicholette D Palmer; J Jeffrey Carr; Lynne E Wagenknecht; R Caresse Hightower; Jianzhao Xu; S Carrie Smith; Dennis J Dietzen; Carl D Langefeld; Barry I Freedman
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2013-12-20
Journal Detail:
Title:  The Journal of clinical endocrinology and metabolism     Volume:  99     ISSN:  1945-7197     ISO Abbreviation:  J. Clin. Endocrinol. Metab.     Publication Date:  2014 Jan 
Date Detail:
Created Date:  2014-01-03     Completed Date:  2014-03-12     Revised Date:  2014-04-16    
Medline Journal Info:
Nlm Unique ID:  0375362     Medline TA:  J Clin Endocrinol Metab     Country:  United States    
Other Details:
Languages:  eng     Pagination:  315-21     Citation Subset:  AIM; IM    
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MeSH Terms
Descriptor/Qualifier:
Adult
African Americans
Aged
Biological Markers / blood
Bone Density / physiology*
Bone Morphogenetic Proteins / blood*
Carotid Artery Diseases / blood*,  ethnology
Cross-Sectional Studies
Diabetes Complications / blood,  ethnology
Female
Genetic Markers
Humans
Male
Middle Aged
Plaque, Atherosclerotic / blood*,  complications,  ethnology
Sex Factors
Vascular Calcification / blood*,  complications,  ethnology
Grant Support
ID/Acronym/Agency:
AR48797/AR/NIAMS NIH HHS; HL67348/HL/NHLBI NIH HHS; M01RR07122/RR/NCRR NIH HHS; R01 DK071891/DK/NIDDK NIH HHS; R01 DK089137/DK/NIDDK NIH HHS; R01DK071891/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Biological Markers; 0/Bone Morphogenetic Proteins; 0/Genetic Markers; 0/SOST protein, human

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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