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The Impact of Nusinersen Treatment on Respiratory Function in Patients with Spinal Muscular Atrophy: A Systematic Review
: This systematic review evaluated the impact of nusinersen therapy on respiratory health and function in individuals with spinal muscular atrophy (SMA) and determined whether nusinersen improves pulmonary function, focusing on differences based on patient age and the timing of treatment initiation....
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Published in: | Journal of clinical medicine 2024-10, Vol.13 (21), p.6306 |
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creator | Aldukain, Mona Aldukain, Ali Hobani, Assal Barakat, Abdulmalik Alsayyed, Lujain Alomar, Maher Zain Al-Abeden, Maha Saad Alzoum, Nora Asseri, Ali Alsuheel |
description | : This systematic review evaluated the impact of nusinersen therapy on respiratory health and function in individuals with spinal muscular atrophy (SMA) and determined whether nusinersen improves pulmonary function, focusing on differences based on patient age and the timing of treatment initiation.
: A systematic search of PubMed, Ovid Medline, ScienceDirect, and Web of Science databases was conducted up to January 2024 in accordance with the PRISMA guidelines. Thirteen studies were included, comprising clinical trials, observational studies, and case series that focused on respiratory outcomes in SMA patients treated with nusinersen. The data on study design, participant characteristics, nusinersen intervention, respiratory outcomes, and adverse events were extracted. The Joanna Briggs Institute Critical Appraisal Tool was used to assess study quality. A narrative synthesis was conducted to address the heterogeneity of the studies.
: This review found a general trend of improvement in pulmonary function, specifically in forced vital capacity (FVC), although the extent and duration of improvement varied across the studies. Peak cough flow (PCF) and peak expiratory flow (PEF) showed positive trends in some studies, although the results were not consistently significant. Respiratory function improvements were frequently observed, particularly in younger patients and those treated earlier.
: Nusinersen appears to enhance respiratory function and improve motor outcomes in SMA patients, especially with early treatment. However, further research is needed to fully understand its mechanisms and long-term effects on respiratory health in SMA. |
doi_str_mv | 10.3390/jcm13216306 |
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: A systematic search of PubMed, Ovid Medline, ScienceDirect, and Web of Science databases was conducted up to January 2024 in accordance with the PRISMA guidelines. Thirteen studies were included, comprising clinical trials, observational studies, and case series that focused on respiratory outcomes in SMA patients treated with nusinersen. The data on study design, participant characteristics, nusinersen intervention, respiratory outcomes, and adverse events were extracted. The Joanna Briggs Institute Critical Appraisal Tool was used to assess study quality. A narrative synthesis was conducted to address the heterogeneity of the studies.
: This review found a general trend of improvement in pulmonary function, specifically in forced vital capacity (FVC), although the extent and duration of improvement varied across the studies. Peak cough flow (PCF) and peak expiratory flow (PEF) showed positive trends in some studies, although the results were not consistently significant. Respiratory function improvements were frequently observed, particularly in younger patients and those treated earlier.
: Nusinersen appears to enhance respiratory function and improve motor outcomes in SMA patients, especially with early treatment. However, further research is needed to fully understand its mechanisms and long-term effects on respiratory health in SMA.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm13216306</identifier><identifier>PMID: 39518446</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adults ; Analysis ; Atrophy ; Care and treatment ; Content analysis ; Diagnosis ; Drug therapy ; Gene expression ; Genetic aspects ; Life expectancy ; Motor neurons ; Patient outcomes ; Pediatrics ; Pulmonary manifestations of general diseases ; Research methodology ; Respiration ; Spinal muscular atrophy ; Systematic Review</subject><ispartof>Journal of clinical medicine, 2024-10, Vol.13 (21), p.6306</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c365t-b3276a19fce0f60c7711bb26b7912a0cc42f9696826eb9e12473440c0b68eb223</cites><orcidid>0009-0008-5634-8432 ; 0000-0001-9858-9789</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3126038790/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3126038790?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39518446$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aldukain, Mona</creatorcontrib><creatorcontrib>Aldukain, Ali</creatorcontrib><creatorcontrib>Hobani, Assal</creatorcontrib><creatorcontrib>Barakat, Abdulmalik</creatorcontrib><creatorcontrib>Alsayyed, Lujain</creatorcontrib><creatorcontrib>Alomar, Maher</creatorcontrib><creatorcontrib>Zain Al-Abeden, Maha Saad</creatorcontrib><creatorcontrib>Alzoum, Nora</creatorcontrib><creatorcontrib>Asseri, Ali Alsuheel</creatorcontrib><title>The Impact of Nusinersen Treatment on Respiratory Function in Patients with Spinal Muscular Atrophy: A Systematic Review</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>: This systematic review evaluated the impact of nusinersen therapy on respiratory health and function in individuals with spinal muscular atrophy (SMA) and determined whether nusinersen improves pulmonary function, focusing on differences based on patient age and the timing of treatment initiation.
: A systematic search of PubMed, Ovid Medline, ScienceDirect, and Web of Science databases was conducted up to January 2024 in accordance with the PRISMA guidelines. Thirteen studies were included, comprising clinical trials, observational studies, and case series that focused on respiratory outcomes in SMA patients treated with nusinersen. The data on study design, participant characteristics, nusinersen intervention, respiratory outcomes, and adverse events were extracted. The Joanna Briggs Institute Critical Appraisal Tool was used to assess study quality. A narrative synthesis was conducted to address the heterogeneity of the studies.
: This review found a general trend of improvement in pulmonary function, specifically in forced vital capacity (FVC), although the extent and duration of improvement varied across the studies. Peak cough flow (PCF) and peak expiratory flow (PEF) showed positive trends in some studies, although the results were not consistently significant. Respiratory function improvements were frequently observed, particularly in younger patients and those treated earlier.
: Nusinersen appears to enhance respiratory function and improve motor outcomes in SMA patients, especially with early treatment. However, further research is needed to fully understand its mechanisms and long-term effects on respiratory health in SMA.</description><subject>Adults</subject><subject>Analysis</subject><subject>Atrophy</subject><subject>Care and treatment</subject><subject>Content analysis</subject><subject>Diagnosis</subject><subject>Drug therapy</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Life expectancy</subject><subject>Motor neurons</subject><subject>Patient outcomes</subject><subject>Pediatrics</subject><subject>Pulmonary manifestations of general diseases</subject><subject>Research methodology</subject><subject>Respiration</subject><subject>Spinal muscular atrophy</subject><subject>Systematic Review</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkl1vFCEUhonR2Kb2yntD4o2J2crXwOCN2TRWm9SP2PWaMPRMl80MjMC07r-X2lq3RriAvDznPXA4CD2n5IhzTd5s3Eg5o5IT-QjtM6LUgvCWP97Z76HDnDekjrYVjKqnaI_rhrZCyH30c7UGfDpO1hUce_x5zj5AyhDwKoEtI4SqB_wN8uSTLTFt8ckcXPFV9AF_tcVXJONrX9b4fPLBDvjTnN082ISXJcVpvX2Ll_h8mwuMlXbV68rD9TP0pLdDhsO79QB9P3m_Ov64OPvy4fR4ebZwXDZl0XGmpKW6d0B6SZxSlHYdk53SlFninGC9llq2TEKngTKhuBDEkU620DHGD9C7W99p7ka4cPW2yQ5mSn60aWui9ebhSfBrcxmvDKWNkKSh1eHVnUOKP2bIxYw-OxgGGyDO2XDKWlVzsqaiL_9BN3FOtSa_KVl_Q2nyl7q0Axgf-lgTuxtTs2xpw0WjiajU0X-oOi9g9C4G6H3VHwS8vg1wKeacoL9_JCXmplnMTrNU-sVuXe7ZP63BfwGdCLkq</recordid><startdate>20241022</startdate><enddate>20241022</enddate><creator>Aldukain, Mona</creator><creator>Aldukain, Ali</creator><creator>Hobani, Assal</creator><creator>Barakat, Abdulmalik</creator><creator>Alsayyed, Lujain</creator><creator>Alomar, Maher</creator><creator>Zain Al-Abeden, Maha Saad</creator><creator>Alzoum, Nora</creator><creator>Asseri, Ali Alsuheel</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0009-0008-5634-8432</orcidid><orcidid>https://orcid.org/0000-0001-9858-9789</orcidid></search><sort><creationdate>20241022</creationdate><title>The Impact of Nusinersen Treatment on Respiratory Function in Patients with Spinal Muscular Atrophy: A Systematic Review</title><author>Aldukain, Mona ; Aldukain, Ali ; Hobani, Assal ; Barakat, Abdulmalik ; Alsayyed, Lujain ; Alomar, Maher ; Zain Al-Abeden, Maha Saad ; Alzoum, Nora ; Asseri, Ali Alsuheel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-b3276a19fce0f60c7711bb26b7912a0cc42f9696826eb9e12473440c0b68eb223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adults</topic><topic>Analysis</topic><topic>Atrophy</topic><topic>Care and treatment</topic><topic>Content analysis</topic><topic>Diagnosis</topic><topic>Drug therapy</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Life expectancy</topic><topic>Motor neurons</topic><topic>Patient outcomes</topic><topic>Pediatrics</topic><topic>Pulmonary manifestations of general diseases</topic><topic>Research methodology</topic><topic>Respiration</topic><topic>Spinal muscular atrophy</topic><topic>Systematic Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aldukain, Mona</creatorcontrib><creatorcontrib>Aldukain, Ali</creatorcontrib><creatorcontrib>Hobani, Assal</creatorcontrib><creatorcontrib>Barakat, Abdulmalik</creatorcontrib><creatorcontrib>Alsayyed, Lujain</creatorcontrib><creatorcontrib>Alomar, Maher</creatorcontrib><creatorcontrib>Zain Al-Abeden, Maha Saad</creatorcontrib><creatorcontrib>Alzoum, Nora</creatorcontrib><creatorcontrib>Asseri, Ali Alsuheel</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aldukain, Mona</au><au>Aldukain, Ali</au><au>Hobani, Assal</au><au>Barakat, Abdulmalik</au><au>Alsayyed, Lujain</au><au>Alomar, Maher</au><au>Zain Al-Abeden, Maha Saad</au><au>Alzoum, Nora</au><au>Asseri, Ali Alsuheel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Impact of Nusinersen Treatment on Respiratory Function in Patients with Spinal Muscular Atrophy: A Systematic Review</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2024-10-22</date><risdate>2024</risdate><volume>13</volume><issue>21</issue><spage>6306</spage><pages>6306-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>: This systematic review evaluated the impact of nusinersen therapy on respiratory health and function in individuals with spinal muscular atrophy (SMA) and determined whether nusinersen improves pulmonary function, focusing on differences based on patient age and the timing of treatment initiation.
: A systematic search of PubMed, Ovid Medline, ScienceDirect, and Web of Science databases was conducted up to January 2024 in accordance with the PRISMA guidelines. Thirteen studies were included, comprising clinical trials, observational studies, and case series that focused on respiratory outcomes in SMA patients treated with nusinersen. The data on study design, participant characteristics, nusinersen intervention, respiratory outcomes, and adverse events were extracted. The Joanna Briggs Institute Critical Appraisal Tool was used to assess study quality. A narrative synthesis was conducted to address the heterogeneity of the studies.
: This review found a general trend of improvement in pulmonary function, specifically in forced vital capacity (FVC), although the extent and duration of improvement varied across the studies. Peak cough flow (PCF) and peak expiratory flow (PEF) showed positive trends in some studies, although the results were not consistently significant. Respiratory function improvements were frequently observed, particularly in younger patients and those treated earlier.
: Nusinersen appears to enhance respiratory function and improve motor outcomes in SMA patients, especially with early treatment. However, further research is needed to fully understand its mechanisms and long-term effects on respiratory health in SMA.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39518446</pmid><doi>10.3390/jcm13216306</doi><orcidid>https://orcid.org/0009-0008-5634-8432</orcidid><orcidid>https://orcid.org/0000-0001-9858-9789</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adults Analysis Atrophy Care and treatment Content analysis Diagnosis Drug therapy Gene expression Genetic aspects Life expectancy Motor neurons Patient outcomes Pediatrics Pulmonary manifestations of general diseases Research methodology Respiration Spinal muscular atrophy Systematic Review |
title | The Impact of Nusinersen Treatment on Respiratory Function in Patients with Spinal Muscular Atrophy: A Systematic Review |
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