Publication:
Effects of statins vs. non-statin lipid-lowering therapy on bone formation and bone mineral density biomarkers in patients with hyperlipidemia

dc.contributor.authorChuengsamarn S.
dc.contributor.authorRattanamongkoulgul S.
dc.contributor.authorSuwanwalaikorn S.
dc.contributor.authorWattanasirichaigoon S.
dc.contributor.authorKaufman L.
dc.date.accessioned2021-04-05T03:36:42Z
dc.date.available2021-04-05T03:36:42Z
dc.date.issued2010
dc.date.issuedBE2553
dc.description.abstractIntroduction: The 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, named statins, are well-established cholesterol-lowering drugs able to reduce cardiovascular risk in hypercholesterolemic patients. The possible effect of statin on bone tissue, so-called pleiotropic effects has received particular attention. Studies reported a positive effect of statin on bone tissue in both of animal and human study by enhancing the expression of the bone morphogenetic proteins (BMPs), in particular of BMP2, which in turn leads to osteoblast differentiation and bone formation including interfering with osteoclastic activity. In a systematic review, the lipophilic statin as simvastatin had positive effect to bone mineral density (BMD) better than the more hydrophilic statin such as atorvastatin and fluvastatin. This study was aimed to compare efficacy of medical therapy between HMG-CoA reductase inhibitor and non-HMG-CoA reductase inhibitor group to changing of bone mineral density and bone markers in the patients with hyperlipidemia. Materials and methods: A prospective randomized control trial study enrolled the 212 hyperlipidemia with osteopenia patients to study in year 2006-2008. All subjects were randomized to 2 groups between statin and non-statin group; the patients were screened by inclusion criteria and measured in bone mineral density (BMD), bone marker and blood chemistry. All data were analyzed by difference of changing in bone marker and BMD between statin and non-statin groups using paired t test. Results: The present study showed 212 hyperlipidemia with osteopenia patients of which 106 patients in statin group had mean age (63.17±9.51 years) and the same number of patients in non-statin group had mean age (60.96±8.9 years). All subjects were 63 patients in male and 149 patients in female. Difference of bone formation marker and BMD between after and before was significantly higher than in statin group and the difference of bone resorption marker was also significantly lower than in statin group. Conclusion: The lipophilic statin as moderate to high dose of simvastatin had beneficial positive effect to increasing BMD and could be additive use for prevention of bone loss in hyperlipidemia patients. © 2010 Elsevier Inc.
dc.format.mimetypeapplication/pdf
dc.identifier.citationBone. Vol 46, No.4 (2010), p.1011-1015
dc.identifier.doi10.1016/j.bone.2009.12.023
dc.identifier.issn87563282
dc.identifier.other2-s2.0-77950532155
dc.identifier.urihttps://hdl.handle.net/20.500.14740/7595
dc.rights.holderScopus
dc.subject.otherAmino terminal telopeptide
dc.subject.otherBone morphogenetic protein 2
dc.subject.otherCarboxy terminal telopeptide
dc.subject.otherCholesterol
dc.subject.otherFibric acid derivative
dc.subject.otherGemfibrozil
dc.subject.otherHigh density lipoprotein cholesterol
dc.subject.otherHydroxymethylglutaryl coenzyme A reductase inhibitor
dc.subject.otherLipid
dc.subject.otherLow density lipoprotein cholesterol
dc.subject.otherSimvastatin
dc.subject.otherTriacylglycerol
dc.subject.otherAdult
dc.subject.otherAged
dc.subject.otherArticle
dc.subject.otherBlood analysis
dc.subject.otherBlood sampling
dc.subject.otherBone density
dc.subject.otherBone tissue
dc.subject.otherCell differentiation
dc.subject.otherClinical trial
dc.subject.otherControlled clinical trial
dc.subject.otherControlled study
dc.subject.otherDiet restriction
dc.subject.otherDrug dose increase
dc.subject.otherFemale
dc.subject.otherHuman
dc.subject.otherHyperlipidemia
dc.subject.otherLipophilicity
dc.subject.otherMajor clinical study
dc.subject.otherMale
dc.subject.otherOssification
dc.subject.otherOsteoblast
dc.subject.otherOsteoclast
dc.subject.otherOsteolysis
dc.subject.otherOsteopenia
dc.subject.otherOsteoporosis
dc.subject.otherPleiotropy
dc.subject.otherProtein expression
dc.subject.otherRandomized controlled trial
dc.subject.otherTreatment outcome
dc.subject.otherAged
dc.subject.otherAntilipemic Agents
dc.subject.otherBone Density
dc.subject.otherBone Diseases, Metabolic
dc.subject.otherFemale
dc.subject.otherGemfibrozil
dc.subject.otherHumans
dc.subject.otherHydroxymethylglutaryl-CoA Reductase Inhibitors
dc.subject.otherHyperlipidemias
dc.subject.otherMale
dc.subject.otherMiddle Aged
dc.subject.otherOsteogenesis
dc.subject.otherPatient Selection
dc.subject.otherProspective Studies
dc.subject.otherSimvastatin
dc.subject.otherTreatment Outcome
dc.titleEffects of statins vs. non-statin lipid-lowering therapy on bone formation and bone mineral density biomarkers in patients with hyperlipidemia
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-77950532155&doi=10.1016%2fj.bone.2009.12.023&partnerID=40&md5=c8b87ffd3f69b207d80322d8d49582bb

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