Comparative Effectiveness of Therapeutic Interventions in Pregnancy and Lactation-Associated Osteoporosis: A Systematic Review and Meta-analysis

Abstract Context The optimal management of pregnancy and lactation-associated osteoporosis (PLO) has not been designated. Objective To systematically review the best available evidence regarding the effect of different therapeutic interventions on bone mineral density (BMD) and risk of fractures in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The journal of clinical endocrinology and metabolism 2024-02, Vol.109 (3), p.879-901
Hauptverfasser: Anagnostis, Panagiotis, Lampropoulou-Adamidou, Kalliopi, Bosdou, Julia K, Trovas, Georgios, Galanis, Petros, Chronopoulos, Efstathios, Goulis, Dimitrios G, Tournis, Symeon
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 901
container_issue 3
container_start_page 879
container_title The journal of clinical endocrinology and metabolism
container_volume 109
creator Anagnostis, Panagiotis
Lampropoulou-Adamidou, Kalliopi
Bosdou, Julia K
Trovas, Georgios
Galanis, Petros
Chronopoulos, Efstathios
Goulis, Dimitrios G
Tournis, Symeon
description Abstract Context The optimal management of pregnancy and lactation-associated osteoporosis (PLO) has not been designated. Objective To systematically review the best available evidence regarding the effect of different therapeutic interventions on bone mineral density (BMD) and risk of fractures in these patients. Methods A comprehensive search was conducted in PubMed/Scopus databases until December 20, 2022. Data were expressed as weighted mean difference (WMD) with 95% CI. The I2 index was employed for heterogeneity. Studies conducted in women with PLO who received any antiosteoporosis therapy were included. Studies including women with secondary causes of osteoporosis or with transient osteoporosis of the hip were excluded. Data extraction was independently completed by 2 researchers. Results Sixty-six studies were included in the qualitative analysis (n = 451 [follow-up time range 6-264 months; age range 19-42 years]). The increase in lumbar spine (LS) BMD with calcium/vitamin D (CaD), bisphosphonates, and teriparatide was 2.0% to 7.5%, 5.0% to 41.5%, and 8.0% to 24.4% at 12 months, and 11.0% to 12.2%, 10.2% to 171.9%, and 24.1% to 32.9% at 24 months, respectively. Femoral neck (FN) BMD increased by 6.1% with CaD, and by 0.7% to 18% and 8.4% to 18.6% with bisphosphonates and teriparatide (18-24 months), respectively. Meta-analysis was performed for 2 interventional studies only. Teriparatide induced a greater increase in LS and FN BMD than CaD (WMD 11.5%, 95% CI 4.9-18.0%, I2 50.9%, and 5.4%, 95% CI 1.2-9.6%, I2 8.1%, respectively). Conclusion Due to high heterogeneity and lack of robust comparative data, no safe conclusions can be made regarding the optimal therapeutic intervention in women with PLO.
doi_str_mv 10.1210/clinem/dgad548
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10876413</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1210/clinem/dgad548</oup_id><sourcerecordid>2865788734</sourcerecordid><originalsourceid>FETCH-LOGICAL-c425t-7bdf9c98b027e7e8644cc8f970a805ef894d4073b1eb02c9ecb7bb732f345a573</originalsourceid><addsrcrecordid>eNqFkUGP0zAQhS0EYsvClSPyEQ7ZtROndrigqlpgpaJFsEjcrIkz6RoldrCdov4LfjIuLSs4cfLI75s39jxCnnN2wUvOLs1gHY6X3Ra6WqgHZMEbUReSN_IhWTBW8qKR5dcz8iTGb4xxIerqMTmrpGSqWtYL8nPtxwkCJLtDetX3aA6Vwxip7-ntHQaYcE7W0GuXMGQpWe8itY5-DLh14MyeguvoBkyCg1asYvTGQsKO3sSEfvLBRxtf0xX9vM8XIxzsPuHO4o_frR8wQQEOhn3GnpJHPQwRn53Oc_Ll7dXt-n2xuXl3vV5tCiPKOhWy7frGNKplpUSJaimEMapvJAPFauxVIzrBZNVyzIhp0LSybWVV9pWooZbVOXlz9J3mdsTO5I8FGPQU7Ahhrz1Y_a_i7J3e-p3mTMml4FV2eHlyCP77jDHp0UaDwwAO_Rx1qZa1VEpWIqMXR9TkVcSA_f0czvQhR33MUZ9yzA0v_n7dPf4nuAy8OgJ-nv5n9guMCq7U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2865788734</pqid></control><display><type>article</type><title>Comparative Effectiveness of Therapeutic Interventions in Pregnancy and Lactation-Associated Osteoporosis: A Systematic Review and Meta-analysis</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><creator>Anagnostis, Panagiotis ; Lampropoulou-Adamidou, Kalliopi ; Bosdou, Julia K ; Trovas, Georgios ; Galanis, Petros ; Chronopoulos, Efstathios ; Goulis, Dimitrios G ; Tournis, Symeon</creator><creatorcontrib>Anagnostis, Panagiotis ; Lampropoulou-Adamidou, Kalliopi ; Bosdou, Julia K ; Trovas, Georgios ; Galanis, Petros ; Chronopoulos, Efstathios ; Goulis, Dimitrios G ; Tournis, Symeon</creatorcontrib><description>Abstract Context The optimal management of pregnancy and lactation-associated osteoporosis (PLO) has not been designated. Objective To systematically review the best available evidence regarding the effect of different therapeutic interventions on bone mineral density (BMD) and risk of fractures in these patients. Methods A comprehensive search was conducted in PubMed/Scopus databases until December 20, 2022. Data were expressed as weighted mean difference (WMD) with 95% CI. The I2 index was employed for heterogeneity. Studies conducted in women with PLO who received any antiosteoporosis therapy were included. Studies including women with secondary causes of osteoporosis or with transient osteoporosis of the hip were excluded. Data extraction was independently completed by 2 researchers. Results Sixty-six studies were included in the qualitative analysis (n = 451 [follow-up time range 6-264 months; age range 19-42 years]). The increase in lumbar spine (LS) BMD with calcium/vitamin D (CaD), bisphosphonates, and teriparatide was 2.0% to 7.5%, 5.0% to 41.5%, and 8.0% to 24.4% at 12 months, and 11.0% to 12.2%, 10.2% to 171.9%, and 24.1% to 32.9% at 24 months, respectively. Femoral neck (FN) BMD increased by 6.1% with CaD, and by 0.7% to 18% and 8.4% to 18.6% with bisphosphonates and teriparatide (18-24 months), respectively. Meta-analysis was performed for 2 interventional studies only. Teriparatide induced a greater increase in LS and FN BMD than CaD (WMD 11.5%, 95% CI 4.9-18.0%, I2 50.9%, and 5.4%, 95% CI 1.2-9.6%, I2 8.1%, respectively). Conclusion Due to high heterogeneity and lack of robust comparative data, no safe conclusions can be made regarding the optimal therapeutic intervention in women with PLO.</description><identifier>ISSN: 0021-972X</identifier><identifier>ISSN: 1945-7197</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgad548</identifier><identifier>PMID: 37708365</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adult ; Bone Density - drug effects ; Bone Density Conservation Agents - therapeutic use ; Diphosphonates - therapeutic use ; Female ; Humans ; Lactation - physiology ; Meta-Analysis ; Osteoporosis - drug therapy ; Osteoporosis - etiology ; Osteoporotic Fractures - epidemiology ; Osteoporotic Fractures - etiology ; Osteoporotic Fractures - prevention &amp; control ; Pregnancy ; Pregnancy Complications - drug therapy ; Pregnancy Complications - therapy ; Teriparatide - therapeutic use ; Treatment Outcome ; Vitamin D - therapeutic use</subject><ispartof>The journal of clinical endocrinology and metabolism, 2024-02, Vol.109 (3), p.879-901</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society.</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-7bdf9c98b027e7e8644cc8f970a805ef894d4073b1eb02c9ecb7bb732f345a573</citedby><cites>FETCH-LOGICAL-c425t-7bdf9c98b027e7e8644cc8f970a805ef894d4073b1eb02c9ecb7bb732f345a573</cites><orcidid>0000-0002-8949-4312</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37708365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anagnostis, Panagiotis</creatorcontrib><creatorcontrib>Lampropoulou-Adamidou, Kalliopi</creatorcontrib><creatorcontrib>Bosdou, Julia K</creatorcontrib><creatorcontrib>Trovas, Georgios</creatorcontrib><creatorcontrib>Galanis, Petros</creatorcontrib><creatorcontrib>Chronopoulos, Efstathios</creatorcontrib><creatorcontrib>Goulis, Dimitrios G</creatorcontrib><creatorcontrib>Tournis, Symeon</creatorcontrib><title>Comparative Effectiveness of Therapeutic Interventions in Pregnancy and Lactation-Associated Osteoporosis: A Systematic Review and Meta-analysis</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Abstract Context The optimal management of pregnancy and lactation-associated osteoporosis (PLO) has not been designated. Objective To systematically review the best available evidence regarding the effect of different therapeutic interventions on bone mineral density (BMD) and risk of fractures in these patients. Methods A comprehensive search was conducted in PubMed/Scopus databases until December 20, 2022. Data were expressed as weighted mean difference (WMD) with 95% CI. The I2 index was employed for heterogeneity. Studies conducted in women with PLO who received any antiosteoporosis therapy were included. Studies including women with secondary causes of osteoporosis or with transient osteoporosis of the hip were excluded. Data extraction was independently completed by 2 researchers. Results Sixty-six studies were included in the qualitative analysis (n = 451 [follow-up time range 6-264 months; age range 19-42 years]). The increase in lumbar spine (LS) BMD with calcium/vitamin D (CaD), bisphosphonates, and teriparatide was 2.0% to 7.5%, 5.0% to 41.5%, and 8.0% to 24.4% at 12 months, and 11.0% to 12.2%, 10.2% to 171.9%, and 24.1% to 32.9% at 24 months, respectively. Femoral neck (FN) BMD increased by 6.1% with CaD, and by 0.7% to 18% and 8.4% to 18.6% with bisphosphonates and teriparatide (18-24 months), respectively. Meta-analysis was performed for 2 interventional studies only. Teriparatide induced a greater increase in LS and FN BMD than CaD (WMD 11.5%, 95% CI 4.9-18.0%, I2 50.9%, and 5.4%, 95% CI 1.2-9.6%, I2 8.1%, respectively). Conclusion Due to high heterogeneity and lack of robust comparative data, no safe conclusions can be made regarding the optimal therapeutic intervention in women with PLO.</description><subject>Adult</subject><subject>Bone Density - drug effects</subject><subject>Bone Density Conservation Agents - therapeutic use</subject><subject>Diphosphonates - therapeutic use</subject><subject>Female</subject><subject>Humans</subject><subject>Lactation - physiology</subject><subject>Meta-Analysis</subject><subject>Osteoporosis - drug therapy</subject><subject>Osteoporosis - etiology</subject><subject>Osteoporotic Fractures - epidemiology</subject><subject>Osteoporotic Fractures - etiology</subject><subject>Osteoporotic Fractures - prevention &amp; control</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - drug therapy</subject><subject>Pregnancy Complications - therapy</subject><subject>Teriparatide - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Vitamin D - therapeutic use</subject><issn>0021-972X</issn><issn>1945-7197</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNqFkUGP0zAQhS0EYsvClSPyEQ7ZtROndrigqlpgpaJFsEjcrIkz6RoldrCdov4LfjIuLSs4cfLI75s39jxCnnN2wUvOLs1gHY6X3Ra6WqgHZMEbUReSN_IhWTBW8qKR5dcz8iTGb4xxIerqMTmrpGSqWtYL8nPtxwkCJLtDetX3aA6Vwxip7-ntHQaYcE7W0GuXMGQpWe8itY5-DLh14MyeguvoBkyCg1asYvTGQsKO3sSEfvLBRxtf0xX9vM8XIxzsPuHO4o_frR8wQQEOhn3GnpJHPQwRn53Oc_Ll7dXt-n2xuXl3vV5tCiPKOhWy7frGNKplpUSJaimEMapvJAPFauxVIzrBZNVyzIhp0LSybWVV9pWooZbVOXlz9J3mdsTO5I8FGPQU7Ahhrz1Y_a_i7J3e-p3mTMml4FV2eHlyCP77jDHp0UaDwwAO_Rx1qZa1VEpWIqMXR9TkVcSA_f0czvQhR33MUZ9yzA0v_n7dPf4nuAy8OgJ-nv5n9guMCq7U</recordid><startdate>20240220</startdate><enddate>20240220</enddate><creator>Anagnostis, Panagiotis</creator><creator>Lampropoulou-Adamidou, Kalliopi</creator><creator>Bosdou, Julia K</creator><creator>Trovas, Georgios</creator><creator>Galanis, Petros</creator><creator>Chronopoulos, Efstathios</creator><creator>Goulis, Dimitrios G</creator><creator>Tournis, Symeon</creator><general>Oxford University Press</general><scope>TOX</scope><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8949-4312</orcidid></search><sort><creationdate>20240220</creationdate><title>Comparative Effectiveness of Therapeutic Interventions in Pregnancy and Lactation-Associated Osteoporosis: A Systematic Review and Meta-analysis</title><author>Anagnostis, Panagiotis ; Lampropoulou-Adamidou, Kalliopi ; Bosdou, Julia K ; Trovas, Georgios ; Galanis, Petros ; Chronopoulos, Efstathios ; Goulis, Dimitrios G ; Tournis, Symeon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-7bdf9c98b027e7e8644cc8f970a805ef894d4073b1eb02c9ecb7bb732f345a573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Bone Density - drug effects</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Diphosphonates - therapeutic use</topic><topic>Female</topic><topic>Humans</topic><topic>Lactation - physiology</topic><topic>Meta-Analysis</topic><topic>Osteoporosis - drug therapy</topic><topic>Osteoporosis - etiology</topic><topic>Osteoporotic Fractures - epidemiology</topic><topic>Osteoporotic Fractures - etiology</topic><topic>Osteoporotic Fractures - prevention &amp; control</topic><topic>Pregnancy</topic><topic>Pregnancy Complications - drug therapy</topic><topic>Pregnancy Complications - therapy</topic><topic>Teriparatide - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Vitamin D - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anagnostis, Panagiotis</creatorcontrib><creatorcontrib>Lampropoulou-Adamidou, Kalliopi</creatorcontrib><creatorcontrib>Bosdou, Julia K</creatorcontrib><creatorcontrib>Trovas, Georgios</creatorcontrib><creatorcontrib>Galanis, Petros</creatorcontrib><creatorcontrib>Chronopoulos, Efstathios</creatorcontrib><creatorcontrib>Goulis, Dimitrios G</creatorcontrib><creatorcontrib>Tournis, Symeon</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anagnostis, Panagiotis</au><au>Lampropoulou-Adamidou, Kalliopi</au><au>Bosdou, Julia K</au><au>Trovas, Georgios</au><au>Galanis, Petros</au><au>Chronopoulos, Efstathios</au><au>Goulis, Dimitrios G</au><au>Tournis, Symeon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Effectiveness of Therapeutic Interventions in Pregnancy and Lactation-Associated Osteoporosis: A Systematic Review and Meta-analysis</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2024-02-20</date><risdate>2024</risdate><volume>109</volume><issue>3</issue><spage>879</spage><epage>901</epage><pages>879-901</pages><issn>0021-972X</issn><issn>1945-7197</issn><eissn>1945-7197</eissn><abstract>Abstract Context The optimal management of pregnancy and lactation-associated osteoporosis (PLO) has not been designated. Objective To systematically review the best available evidence regarding the effect of different therapeutic interventions on bone mineral density (BMD) and risk of fractures in these patients. Methods A comprehensive search was conducted in PubMed/Scopus databases until December 20, 2022. Data were expressed as weighted mean difference (WMD) with 95% CI. The I2 index was employed for heterogeneity. Studies conducted in women with PLO who received any antiosteoporosis therapy were included. Studies including women with secondary causes of osteoporosis or with transient osteoporosis of the hip were excluded. Data extraction was independently completed by 2 researchers. Results Sixty-six studies were included in the qualitative analysis (n = 451 [follow-up time range 6-264 months; age range 19-42 years]). The increase in lumbar spine (LS) BMD with calcium/vitamin D (CaD), bisphosphonates, and teriparatide was 2.0% to 7.5%, 5.0% to 41.5%, and 8.0% to 24.4% at 12 months, and 11.0% to 12.2%, 10.2% to 171.9%, and 24.1% to 32.9% at 24 months, respectively. Femoral neck (FN) BMD increased by 6.1% with CaD, and by 0.7% to 18% and 8.4% to 18.6% with bisphosphonates and teriparatide (18-24 months), respectively. Meta-analysis was performed for 2 interventional studies only. Teriparatide induced a greater increase in LS and FN BMD than CaD (WMD 11.5%, 95% CI 4.9-18.0%, I2 50.9%, and 5.4%, 95% CI 1.2-9.6%, I2 8.1%, respectively). Conclusion Due to high heterogeneity and lack of robust comparative data, no safe conclusions can be made regarding the optimal therapeutic intervention in women with PLO.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>37708365</pmid><doi>10.1210/clinem/dgad548</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0002-8949-4312</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-972X
ispartof The journal of clinical endocrinology and metabolism, 2024-02, Vol.109 (3), p.879-901
issn 0021-972X
1945-7197
1945-7197
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10876413
source Oxford University Press Journals All Titles (1996-Current); MEDLINE
subjects Adult
Bone Density - drug effects
Bone Density Conservation Agents - therapeutic use
Diphosphonates - therapeutic use
Female
Humans
Lactation - physiology
Meta-Analysis
Osteoporosis - drug therapy
Osteoporosis - etiology
Osteoporotic Fractures - epidemiology
Osteoporotic Fractures - etiology
Osteoporotic Fractures - prevention & control
Pregnancy
Pregnancy Complications - drug therapy
Pregnancy Complications - therapy
Teriparatide - therapeutic use
Treatment Outcome
Vitamin D - therapeutic use
title Comparative Effectiveness of Therapeutic Interventions in Pregnancy and Lactation-Associated Osteoporosis: A Systematic Review and Meta-analysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T16%3A53%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparative%20Effectiveness%20of%20Therapeutic%20Interventions%20in%20Pregnancy%20and%20Lactation-Associated%20Osteoporosis:%20A%20Systematic%20Review%20and%20Meta-analysis&rft.jtitle=The%20journal%20of%20clinical%20endocrinology%20and%20metabolism&rft.au=Anagnostis,%20Panagiotis&rft.date=2024-02-20&rft.volume=109&rft.issue=3&rft.spage=879&rft.epage=901&rft.pages=879-901&rft.issn=0021-972X&rft.eissn=1945-7197&rft_id=info:doi/10.1210/clinem/dgad548&rft_dat=%3Cproquest_pubme%3E2865788734%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2865788734&rft_id=info:pmid/37708365&rft_oup_id=10.1210/clinem/dgad548&rfr_iscdi=true