Evidence-based prevention and treatment of osteoporosis after spinal cord injury: a systematic review

Purpose Spinal cord injury (SCI) results in accelerated bone mineral density (BMD) loss and disorganization of trabecular bone architecture. The mechanisms underlying post-SCI osteoporosis are complex and different from other types of osteoporosis. Findings of studies investigating efficacy of pharm...

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Veröffentlicht in:European spine journal 2018-08, Vol.27 (8), p.1798-1814
Hauptverfasser: Soleyman-Jahi, Saeed, Yousefian, Ali, Maheronnaghsh, Radin, Shokraneh, Farhad, Zadegan, Shayan Abdollah, Soltani, Akbar, Hosseini, Seyed Mostafa, Vaccaro, Alexander R., Rahimi-Movaghar, Vafa
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container_end_page 1814
container_issue 8
container_start_page 1798
container_title European spine journal
container_volume 27
creator Soleyman-Jahi, Saeed
Yousefian, Ali
Maheronnaghsh, Radin
Shokraneh, Farhad
Zadegan, Shayan Abdollah
Soltani, Akbar
Hosseini, Seyed Mostafa
Vaccaro, Alexander R.
Rahimi-Movaghar, Vafa
description Purpose Spinal cord injury (SCI) results in accelerated bone mineral density (BMD) loss and disorganization of trabecular bone architecture. The mechanisms underlying post-SCI osteoporosis are complex and different from other types of osteoporosis. Findings of studies investigating efficacy of pharmacological or rehabilitative interventions in SCI-related osteoporosis are controversial. The aim of this study was to review the literature pertaining to prevention and evidence-based treatments of SCI-related osteoporosis. Methods In this systematic review, MEDLINE, EMBASE, PubMed, and the Cochrane Library were used to identify papers from 1946 to December 31, 2015. The search strategy involved the following keywords: spinal cord injury, osteoporosis, and bone loss. Results Finally, 56 studies were included according to the inclusion criteria. Only 16 randomized controlled trials (involving 368 patients) were found. We found following evidences for effectiveness of bisphosphonates in prevention of BMD loss in acute SCI: very low-quality evidence for clodronate and etidronate, low-quality evidence for alendronate, and moderate-quality evidence for zoledronic acid. Low-quality evidence showed no effectiveness for tiludronate. In chronic SCI cases, we found low-quality evidence for effectiveness of vitamin D 3 analogs combined with 1-alpha vitamin D 2 . However, low-quality inconsistent evidence exists for alendronate. For non-pharmacologic interventions, very low-quality evidence exists for effectiveness of standing with or without treadmill walking in acute SCI. Other low-quality evidences indicated that electrical stimulation, tilt-table standing, and ultrasound provide no significant effects. Very low-quality evidence did not show any benefit for low-intensity (3 days per week) cycling with functional electrical stimulator in chronic SCI. Conclusions No recommendations can be made from this review, regarding overall low quality of evidence as a result of high risk of bias, low sample size in most of the studies, and notable heterogeneity in type of intervention, outcome measurement, and duration of treatment. Therefore, future high-quality RCT studies with higher sample sizes and more homogeneity are strongly recommended to provide high-quality evidence and make applicable recommendations for prevention and treatment of SCI-related bone loss.
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The mechanisms underlying post-SCI osteoporosis are complex and different from other types of osteoporosis. Findings of studies investigating efficacy of pharmacological or rehabilitative interventions in SCI-related osteoporosis are controversial. The aim of this study was to review the literature pertaining to prevention and evidence-based treatments of SCI-related osteoporosis. Methods In this systematic review, MEDLINE, EMBASE, PubMed, and the Cochrane Library were used to identify papers from 1946 to December 31, 2015. The search strategy involved the following keywords: spinal cord injury, osteoporosis, and bone loss. Results Finally, 56 studies were included according to the inclusion criteria. Only 16 randomized controlled trials (involving 368 patients) were found. We found following evidences for effectiveness of bisphosphonates in prevention of BMD loss in acute SCI: very low-quality evidence for clodronate and etidronate, low-quality evidence for alendronate, and moderate-quality evidence for zoledronic acid. Low-quality evidence showed no effectiveness for tiludronate. In chronic SCI cases, we found low-quality evidence for effectiveness of vitamin D 3 analogs combined with 1-alpha vitamin D 2 . However, low-quality inconsistent evidence exists for alendronate. For non-pharmacologic interventions, very low-quality evidence exists for effectiveness of standing with or without treadmill walking in acute SCI. Other low-quality evidences indicated that electrical stimulation, tilt-table standing, and ultrasound provide no significant effects. Very low-quality evidence did not show any benefit for low-intensity (3 days per week) cycling with functional electrical stimulator in chronic SCI. Conclusions No recommendations can be made from this review, regarding overall low quality of evidence as a result of high risk of bias, low sample size in most of the studies, and notable heterogeneity in type of intervention, outcome measurement, and duration of treatment. Therefore, future high-quality RCT studies with higher sample sizes and more homogeneity are strongly recommended to provide high-quality evidence and make applicable recommendations for prevention and treatment of SCI-related bone loss.</description><identifier>ISSN: 0940-6719</identifier><identifier>EISSN: 1432-0932</identifier><identifier>DOI: 10.1007/s00586-017-5114-7</identifier><identifier>PMID: 28497215</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Alendronic acid ; Bisphosphonates ; Bone Density - drug effects ; Bone Density - physiology ; Bone Density Conservation Agents - therapeutic use ; Bone loss ; Bone mineral density ; Cancellous bone ; Clinical trials ; Clodronic acid ; Electric Stimulation - methods ; Electrical stimuli ; Etidronic acid ; Female ; Humans ; Male ; Medicine ; Medicine &amp; Public Health ; Neurosurgery ; Osteoporosis ; Osteoporosis - etiology ; Osteoporosis - prevention &amp; control ; Osteoporosis - therapy ; Prevention ; Quality ; Review ; Spinal cord injuries ; Spinal Cord Injuries - complications ; Surgical Orthopedics ; Systematic review ; Ultrasound ; Vitamin D - therapeutic use ; Vitamin D2 ; Vitamin D3 ; Zoledronic acid</subject><ispartof>European spine journal, 2018-08, Vol.27 (8), p.1798-1814</ispartof><rights>Springer-Verlag Berlin Heidelberg 2017</rights><rights>European Spine Journal is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-a074631c29332f08c1c4c26d831b86566a6bbb7f03b7e9e5ccd27035fd79eef03</citedby><cites>FETCH-LOGICAL-c372t-a074631c29332f08c1c4c26d831b86566a6bbb7f03b7e9e5ccd27035fd79eef03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00586-017-5114-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00586-017-5114-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28497215$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Soleyman-Jahi, Saeed</creatorcontrib><creatorcontrib>Yousefian, Ali</creatorcontrib><creatorcontrib>Maheronnaghsh, Radin</creatorcontrib><creatorcontrib>Shokraneh, Farhad</creatorcontrib><creatorcontrib>Zadegan, Shayan Abdollah</creatorcontrib><creatorcontrib>Soltani, Akbar</creatorcontrib><creatorcontrib>Hosseini, Seyed Mostafa</creatorcontrib><creatorcontrib>Vaccaro, Alexander R.</creatorcontrib><creatorcontrib>Rahimi-Movaghar, Vafa</creatorcontrib><title>Evidence-based prevention and treatment of osteoporosis after spinal cord injury: a systematic review</title><title>European spine journal</title><addtitle>Eur Spine J</addtitle><addtitle>Eur Spine J</addtitle><description>Purpose Spinal cord injury (SCI) results in accelerated bone mineral density (BMD) loss and disorganization of trabecular bone architecture. The mechanisms underlying post-SCI osteoporosis are complex and different from other types of osteoporosis. Findings of studies investigating efficacy of pharmacological or rehabilitative interventions in SCI-related osteoporosis are controversial. The aim of this study was to review the literature pertaining to prevention and evidence-based treatments of SCI-related osteoporosis. Methods In this systematic review, MEDLINE, EMBASE, PubMed, and the Cochrane Library were used to identify papers from 1946 to December 31, 2015. The search strategy involved the following keywords: spinal cord injury, osteoporosis, and bone loss. Results Finally, 56 studies were included according to the inclusion criteria. Only 16 randomized controlled trials (involving 368 patients) were found. We found following evidences for effectiveness of bisphosphonates in prevention of BMD loss in acute SCI: very low-quality evidence for clodronate and etidronate, low-quality evidence for alendronate, and moderate-quality evidence for zoledronic acid. Low-quality evidence showed no effectiveness for tiludronate. In chronic SCI cases, we found low-quality evidence for effectiveness of vitamin D 3 analogs combined with 1-alpha vitamin D 2 . However, low-quality inconsistent evidence exists for alendronate. For non-pharmacologic interventions, very low-quality evidence exists for effectiveness of standing with or without treadmill walking in acute SCI. Other low-quality evidences indicated that electrical stimulation, tilt-table standing, and ultrasound provide no significant effects. Very low-quality evidence did not show any benefit for low-intensity (3 days per week) cycling with functional electrical stimulator in chronic SCI. Conclusions No recommendations can be made from this review, regarding overall low quality of evidence as a result of high risk of bias, low sample size in most of the studies, and notable heterogeneity in type of intervention, outcome measurement, and duration of treatment. Therefore, future high-quality RCT studies with higher sample sizes and more homogeneity are strongly recommended to provide high-quality evidence and make applicable recommendations for prevention and treatment of SCI-related bone loss.</description><subject>Alendronic acid</subject><subject>Bisphosphonates</subject><subject>Bone Density - drug effects</subject><subject>Bone Density - physiology</subject><subject>Bone Density Conservation Agents - therapeutic use</subject><subject>Bone loss</subject><subject>Bone mineral density</subject><subject>Cancellous bone</subject><subject>Clinical trials</subject><subject>Clodronic acid</subject><subject>Electric Stimulation - methods</subject><subject>Electrical stimuli</subject><subject>Etidronic acid</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Neurosurgery</subject><subject>Osteoporosis</subject><subject>Osteoporosis - etiology</subject><subject>Osteoporosis - prevention &amp; control</subject><subject>Osteoporosis - therapy</subject><subject>Prevention</subject><subject>Quality</subject><subject>Review</subject><subject>Spinal cord injuries</subject><subject>Spinal Cord Injuries - complications</subject><subject>Surgical Orthopedics</subject><subject>Systematic review</subject><subject>Ultrasound</subject><subject>Vitamin D - therapeutic use</subject><subject>Vitamin D2</subject><subject>Vitamin D3</subject><subject>Zoledronic acid</subject><issn>0940-6719</issn><issn>1432-0932</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kcGKFDEQhoMo7uzqA3iRgBcv0aqkO-l4k2V1hQUveg7pdLVkmO60SffKvP1mmFVB8BSofPUVVT9jrxDeIYB5XwDaTgtAI1rERpgnbIeNkgKskk_ZDmwDQhu0F-yylD0Athb0c3Yhu8Yaie2O0c19HGgOJHpfaOBLpnua15hm7ueBr5n8OtUCTyNPZaW0pJxKLNyPK2Veljj7Aw8pDzzO-y0fP3DPy7GSk19j4FUX6dcL9mz0h0IvH98r9v3TzbfrW3H39fOX6493IigjV-HBNFphkFYpOUIXMDRB6qFT2He61drrvu_NCKo3ZKkNYZAGVDsOxhLV8hV7e_YuOf3cqKxuiiXQ4eBnSltx2FmLaECair75B92nLddlipPQoUJQcBLimQp165JpdEuOk89Hh-BOGbhzBq5m4E4ZuJP59aN56yca_nT8PnoF5Bko9Wv-Qfnv6P9bHwBs-ZIl</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Soleyman-Jahi, Saeed</creator><creator>Yousefian, Ali</creator><creator>Maheronnaghsh, Radin</creator><creator>Shokraneh, Farhad</creator><creator>Zadegan, Shayan Abdollah</creator><creator>Soltani, Akbar</creator><creator>Hosseini, Seyed Mostafa</creator><creator>Vaccaro, Alexander R.</creator><creator>Rahimi-Movaghar, Vafa</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20180801</creationdate><title>Evidence-based prevention and treatment of osteoporosis after spinal cord injury: a systematic review</title><author>Soleyman-Jahi, Saeed ; Yousefian, Ali ; Maheronnaghsh, Radin ; Shokraneh, Farhad ; Zadegan, Shayan Abdollah ; Soltani, Akbar ; Hosseini, Seyed Mostafa ; Vaccaro, Alexander R. ; Rahimi-Movaghar, Vafa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-a074631c29332f08c1c4c26d831b86566a6bbb7f03b7e9e5ccd27035fd79eef03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alendronic acid</topic><topic>Bisphosphonates</topic><topic>Bone Density - drug effects</topic><topic>Bone Density - physiology</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Bone loss</topic><topic>Bone mineral density</topic><topic>Cancellous bone</topic><topic>Clinical trials</topic><topic>Clodronic acid</topic><topic>Electric Stimulation - methods</topic><topic>Electrical stimuli</topic><topic>Etidronic acid</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Neurosurgery</topic><topic>Osteoporosis</topic><topic>Osteoporosis - etiology</topic><topic>Osteoporosis - prevention &amp; control</topic><topic>Osteoporosis - therapy</topic><topic>Prevention</topic><topic>Quality</topic><topic>Review</topic><topic>Spinal cord injuries</topic><topic>Spinal Cord Injuries - complications</topic><topic>Surgical Orthopedics</topic><topic>Systematic review</topic><topic>Ultrasound</topic><topic>Vitamin D - therapeutic use</topic><topic>Vitamin D2</topic><topic>Vitamin D3</topic><topic>Zoledronic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soleyman-Jahi, Saeed</creatorcontrib><creatorcontrib>Yousefian, Ali</creatorcontrib><creatorcontrib>Maheronnaghsh, Radin</creatorcontrib><creatorcontrib>Shokraneh, Farhad</creatorcontrib><creatorcontrib>Zadegan, Shayan Abdollah</creatorcontrib><creatorcontrib>Soltani, Akbar</creatorcontrib><creatorcontrib>Hosseini, Seyed Mostafa</creatorcontrib><creatorcontrib>Vaccaro, Alexander R.</creatorcontrib><creatorcontrib>Rahimi-Movaghar, Vafa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; 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The mechanisms underlying post-SCI osteoporosis are complex and different from other types of osteoporosis. Findings of studies investigating efficacy of pharmacological or rehabilitative interventions in SCI-related osteoporosis are controversial. The aim of this study was to review the literature pertaining to prevention and evidence-based treatments of SCI-related osteoporosis. Methods In this systematic review, MEDLINE, EMBASE, PubMed, and the Cochrane Library were used to identify papers from 1946 to December 31, 2015. The search strategy involved the following keywords: spinal cord injury, osteoporosis, and bone loss. Results Finally, 56 studies were included according to the inclusion criteria. Only 16 randomized controlled trials (involving 368 patients) were found. We found following evidences for effectiveness of bisphosphonates in prevention of BMD loss in acute SCI: very low-quality evidence for clodronate and etidronate, low-quality evidence for alendronate, and moderate-quality evidence for zoledronic acid. Low-quality evidence showed no effectiveness for tiludronate. In chronic SCI cases, we found low-quality evidence for effectiveness of vitamin D 3 analogs combined with 1-alpha vitamin D 2 . However, low-quality inconsistent evidence exists for alendronate. For non-pharmacologic interventions, very low-quality evidence exists for effectiveness of standing with or without treadmill walking in acute SCI. Other low-quality evidences indicated that electrical stimulation, tilt-table standing, and ultrasound provide no significant effects. Very low-quality evidence did not show any benefit for low-intensity (3 days per week) cycling with functional electrical stimulator in chronic SCI. Conclusions No recommendations can be made from this review, regarding overall low quality of evidence as a result of high risk of bias, low sample size in most of the studies, and notable heterogeneity in type of intervention, outcome measurement, and duration of treatment. Therefore, future high-quality RCT studies with higher sample sizes and more homogeneity are strongly recommended to provide high-quality evidence and make applicable recommendations for prevention and treatment of SCI-related bone loss.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28497215</pmid><doi>10.1007/s00586-017-5114-7</doi><tpages>17</tpages></addata></record>
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subjects Alendronic acid
Bisphosphonates
Bone Density - drug effects
Bone Density - physiology
Bone Density Conservation Agents - therapeutic use
Bone loss
Bone mineral density
Cancellous bone
Clinical trials
Clodronic acid
Electric Stimulation - methods
Electrical stimuli
Etidronic acid
Female
Humans
Male
Medicine
Medicine & Public Health
Neurosurgery
Osteoporosis
Osteoporosis - etiology
Osteoporosis - prevention & control
Osteoporosis - therapy
Prevention
Quality
Review
Spinal cord injuries
Spinal Cord Injuries - complications
Surgical Orthopedics
Systematic review
Ultrasound
Vitamin D - therapeutic use
Vitamin D2
Vitamin D3
Zoledronic acid
title Evidence-based prevention and treatment of osteoporosis after spinal cord injury: a systematic review
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