Literature DB >> 19416946

The decrease of soluble RAGE levels in rheumatoid arthritis patients following hormone replacement therapy is associated with increased bone mineral density and diminished bone/cartilage turnover: a randomized controlled trial.

Rille Pullerits1, Helena Forsblad d'Elia, Andrej Tarkowski, Hans Carlsten.   

Abstract

OBJECTIVE: The aim of the study was to prospectively investigate the effects of HRT on serum soluble receptor for advanced glycation end product (sRAGE) levels in RA patients and to determine whether sRAGE production is related to bone/cartilage metabolism.
METHODS: Eighty-eight post-menopausal RA patients were randomized to receive vitamin D3 and calcium supplementation with or without HRT (oestradiol plus noretisterone acetate). The levels of total sRAGE in sera were measured before, 1 and 2 years after treatment initiation. Potential associations between sRAGE levels, bone/cartilage metabolic markers and BMD were investigated.
RESULTS: Patients receiving HRT displayed significantly decreased levels of serum sRAGE at 1 and 2 years as compared with levels at study entry. The increase in serum oestradiol was associated with the decline in sRAGE levels. Importantly, sRAGE levels at baseline significantly correlated with bone/cartilage turnover markers including C-terminal propeptide of type I procollagen, carboxyterminal telopeptide of type I collagen and cartilage oligomeric matrix protein, and the decrease of sRAGE levels paralleled with diminished concentration of these molecules. BMD in hip and femoral neck and progression of Larsen score at 1 year were associated with baseline sRAGE levels. The decline in sRAGE levels significantly correlated with an increase in total BMD following 2 years of treatment in patients receiving HRT but not in the control group.
CONCLUSION: Our findings suggest that HRT decreases the levels of endogenous sRAGE in post-menopausal RA patients implicating its role in sRAGE regulation. In addition, serum sRAGE was associated with BMD and markers of bone/cartilage metabolism. These data suggest that sRAGE is involved directly or indirectly in bone metabolism. Trial registration. Current Controlled Trials, ISRCTN46523456, http://www.controlled-trials.com/isrctn/search.html?srch=ISRCTN46523456.

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Year:  2009        PMID: 19416946     DOI: 10.1093/rheumatology/kep079

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  5 in total

Review 1.  Soluble RAGEs - Prospects for treating & tracking metabolic and inflammatory disease.

Authors:  Ann Marie Schmidt
Journal:  Vascul Pharmacol       Date:  2015-06-27       Impact factor: 5.773

Review 2.  RAGE Signaling in Skeletal Biology.

Authors:  Lilian I Plotkin; Alyson L Essex; Hannah M Davis
Journal:  Curr Osteoporos Rep       Date:  2019-02       Impact factor: 5.096

Review 3.  Relationship of Advanced Glycation End Products With Cardiovascular Disease in Menopausal Women.

Authors:  Magdalena Pertynska-Marczewska; Zaher Merhi
Journal:  Reprod Sci       Date:  2014-09-16       Impact factor: 3.060

4.  Soluble Forms of the Receptor for Advanced Glycation Endproducts (RAGE) in Periodontitis.

Authors:  Laurent Detzen; Bin Cheng; Ching-Yuan Chen; Panos N Papapanou; Evanthia Lalla
Journal:  Sci Rep       Date:  2019-06-03       Impact factor: 4.379

5.  Dangguijihwang-tang and Dangguijakyak-san Prevent Menopausal Symptoms and Dangguijihwang-tang Prevents Articular Cartilage Deterioration in Ovariectomized Obese Rats with Monoiodoacetate-Induced Osteoarthritis.

Authors:  Hye Won Lee; Byung-Seob Ko; Sunmin Park; Suna Kang; Jin Ah Ryuk; Min Joo Kim
Journal:  Evid Based Complement Alternat Med       Date:  2017-10-24       Impact factor: 2.629

  5 in total

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