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Respiratory parameters on diagnostic sleep studies predict survival in patients with amyotrophic lateral sclerosis
Objective In amyotrophic lateral sclerosis (ALS), respiratory muscle involvement and sleep-disordered breathing relate to worse prognosis. The present study investigated whether respiratory outcomes on first-ever sleep studies predict survival in patients with ALS, specifically taking into account s...
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Published in: | Journal of neurology 2021-11, Vol.268 (11), p.4321-4331 |
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creator | Engel, Markus Glatz, Christian Helmle, Cornelia Young, Peter Dräger, Bianca Boentert, Matthias |
description | Objective
In amyotrophic lateral sclerosis (ALS), respiratory muscle involvement and sleep-disordered breathing relate to worse prognosis. The present study investigated whether respiratory outcomes on first-ever sleep studies predict survival in patients with ALS, specifically taking into account subsequent initiation of non-invasive ventilation (NIV).
Methods
From patients with ALS, baseline sleep study records, transcutaneous capnometry, early morning blood gas analysis, survival data and clinical disease characteristics were retrospectively analyzed. Patients were stratified according to whether enduring NIV was consecutively established (“NIV(+)”) or not (“NIV(–)”).
Results
Among the study cohort (
n
= 158, 72 female, 51 with bulbar onset ALS, 105 deceased) sleep-disordered breathing was present at baseline evaluation in 97 patients. Early morning base excess (EMBE) > 2 mmol/l predicted nocturnal hypercapnia. Ninety-five patients were NIV(+) and 63 were NIV(–). Survival from baseline sleep studies was significantly reduced in NIV(–) but not in NIV(+) patients with nocturnal CO
2
tension ≥ 50 mmHg, apnea hypopnea index ≥ 5/h, and EMBE > 2 mmol/l. Hazard ratio for EMBE > 2 mmol/l was increased in NIV(–) patients only, and EMBE independently predicted survival in both NIV(–) and NIV(+) patients. Furthermore, EMBE on baseline sleep studies was the only predictor for survival from symptom onset, and hazard ratio for shorter survival was markedly higher in the NIV(–) than the NIV(+) group (2.85,
p
= 0.005, vs. 1.71,
p
= 0.042).
Interpretation: In patients with ALS, EMBE > 2 mmol/l predicts nocturnal hypercapnia and shorter survival. Negative effects of sleep-disordered breathing on survival are statistically abolished by sustained NIV. |
doi_str_mv | 10.1007/s00415-021-10563-0 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8505303</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2516223359</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-f846d1e9b764d64c6c8af6aeb094212a18142f8d57fd81705e5ca681f8e66dac3</originalsourceid><addsrcrecordid>eNp9kc2LFDEQxRtR3HH1H_AgAS9eWiufk7kIsugqLAii55BJV89k6e60qfTI_Pdmd9b14-Aph_d7L1X1muY5h9ccYP2GABTXLQjectBGtvCgWXElRcuV3jxsViAVtFpqddY8IboGAFuFx82ZlNaC4XzV5C9Ic8y-pHxks89-xIKZWJpYF_1uSlRiYDQgzozK0kUkNmfsYiiMlnyIBz-wOFVriTgVYj9i2TM_HlPJad5X7-BrYIUoDJgTRXraPOr9QPjs7j1vvn14__XiY3v1-fLTxburNqi1Km1vlek4brZrozqjggnW98bjFjZKcOG55Ur0ttPrvrN8DRp18Mby3qIxnQ_yvHl7yp2X7YhdqOPVOdyc4-jz0SUf3d_KFPdulw7OatASZA14dReQ0_cFqbgxUsBh8BOmhZzQ3Aghpd5U9OU_6HVa8lTXq5QFK7SSN5Q4UaEegjL298NwcDeVulOlrlbqbit1UE0v_lzj3vKrwwrIE0BVmnaYf__9n9ifo8-wBA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2580825439</pqid></control><display><type>article</type><title>Respiratory parameters on diagnostic sleep studies predict survival in patients with amyotrophic lateral sclerosis</title><source>Springer Nature</source><creator>Engel, Markus ; Glatz, Christian ; Helmle, Cornelia ; Young, Peter ; Dräger, Bianca ; Boentert, Matthias</creator><creatorcontrib>Engel, Markus ; Glatz, Christian ; Helmle, Cornelia ; Young, Peter ; Dräger, Bianca ; Boentert, Matthias</creatorcontrib><description>Objective
In amyotrophic lateral sclerosis (ALS), respiratory muscle involvement and sleep-disordered breathing relate to worse prognosis. The present study investigated whether respiratory outcomes on first-ever sleep studies predict survival in patients with ALS, specifically taking into account subsequent initiation of non-invasive ventilation (NIV).
Methods
From patients with ALS, baseline sleep study records, transcutaneous capnometry, early morning blood gas analysis, survival data and clinical disease characteristics were retrospectively analyzed. Patients were stratified according to whether enduring NIV was consecutively established (“NIV(+)”) or not (“NIV(–)”).
Results
Among the study cohort (
n
= 158, 72 female, 51 with bulbar onset ALS, 105 deceased) sleep-disordered breathing was present at baseline evaluation in 97 patients. Early morning base excess (EMBE) > 2 mmol/l predicted nocturnal hypercapnia. Ninety-five patients were NIV(+) and 63 were NIV(–). Survival from baseline sleep studies was significantly reduced in NIV(–) but not in NIV(+) patients with nocturnal CO
2
tension ≥ 50 mmHg, apnea hypopnea index ≥ 5/h, and EMBE > 2 mmol/l. Hazard ratio for EMBE > 2 mmol/l was increased in NIV(–) patients only, and EMBE independently predicted survival in both NIV(–) and NIV(+) patients. Furthermore, EMBE on baseline sleep studies was the only predictor for survival from symptom onset, and hazard ratio for shorter survival was markedly higher in the NIV(–) than the NIV(+) group (2.85,
p
= 0.005, vs. 1.71,
p
= 0.042).
Interpretation: In patients with ALS, EMBE > 2 mmol/l predicts nocturnal hypercapnia and shorter survival. Negative effects of sleep-disordered breathing on survival are statistically abolished by sustained NIV.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-021-10563-0</identifier><identifier>PMID: 33880611</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amyotrophic lateral sclerosis ; Amyotrophic Lateral Sclerosis - complications ; Amyotrophic Lateral Sclerosis - diagnosis ; Amyotrophic Lateral Sclerosis - therapy ; Apnea ; Blood gas analysis ; Carbon dioxide ; Female ; Humans ; Hypercapnia ; Mechanical ventilation ; Medical prognosis ; Medicine ; Medicine & Public Health ; Neurology ; Neuroradiology ; Neurosciences ; Noninvasive Ventilation ; Original Communication ; Oxygen therapy ; Patients ; Polysomnography ; Respiration ; Respiratory Insufficiency - etiology ; Respiratory Insufficiency - therapy ; Retrospective Studies ; Sleep ; Sleep disorders ; Survival</subject><ispartof>Journal of neurology, 2021-11, Vol.268 (11), p.4321-4331</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-f846d1e9b764d64c6c8af6aeb094212a18142f8d57fd81705e5ca681f8e66dac3</citedby><cites>FETCH-LOGICAL-c474t-f846d1e9b764d64c6c8af6aeb094212a18142f8d57fd81705e5ca681f8e66dac3</cites><orcidid>0000-0001-6133-1397</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33880611$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Engel, Markus</creatorcontrib><creatorcontrib>Glatz, Christian</creatorcontrib><creatorcontrib>Helmle, Cornelia</creatorcontrib><creatorcontrib>Young, Peter</creatorcontrib><creatorcontrib>Dräger, Bianca</creatorcontrib><creatorcontrib>Boentert, Matthias</creatorcontrib><title>Respiratory parameters on diagnostic sleep studies predict survival in patients with amyotrophic lateral sclerosis</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Objective
In amyotrophic lateral sclerosis (ALS), respiratory muscle involvement and sleep-disordered breathing relate to worse prognosis. The present study investigated whether respiratory outcomes on first-ever sleep studies predict survival in patients with ALS, specifically taking into account subsequent initiation of non-invasive ventilation (NIV).
Methods
From patients with ALS, baseline sleep study records, transcutaneous capnometry, early morning blood gas analysis, survival data and clinical disease characteristics were retrospectively analyzed. Patients were stratified according to whether enduring NIV was consecutively established (“NIV(+)”) or not (“NIV(–)”).
Results
Among the study cohort (
n
= 158, 72 female, 51 with bulbar onset ALS, 105 deceased) sleep-disordered breathing was present at baseline evaluation in 97 patients. Early morning base excess (EMBE) > 2 mmol/l predicted nocturnal hypercapnia. Ninety-five patients were NIV(+) and 63 were NIV(–). Survival from baseline sleep studies was significantly reduced in NIV(–) but not in NIV(+) patients with nocturnal CO
2
tension ≥ 50 mmHg, apnea hypopnea index ≥ 5/h, and EMBE > 2 mmol/l. Hazard ratio for EMBE > 2 mmol/l was increased in NIV(–) patients only, and EMBE independently predicted survival in both NIV(–) and NIV(+) patients. Furthermore, EMBE on baseline sleep studies was the only predictor for survival from symptom onset, and hazard ratio for shorter survival was markedly higher in the NIV(–) than the NIV(+) group (2.85,
p
= 0.005, vs. 1.71,
p
= 0.042).
Interpretation: In patients with ALS, EMBE > 2 mmol/l predicts nocturnal hypercapnia and shorter survival. Negative effects of sleep-disordered breathing on survival are statistically abolished by sustained NIV.</description><subject>Amyotrophic lateral sclerosis</subject><subject>Amyotrophic Lateral Sclerosis - complications</subject><subject>Amyotrophic Lateral Sclerosis - diagnosis</subject><subject>Amyotrophic Lateral Sclerosis - therapy</subject><subject>Apnea</subject><subject>Blood gas analysis</subject><subject>Carbon dioxide</subject><subject>Female</subject><subject>Humans</subject><subject>Hypercapnia</subject><subject>Mechanical ventilation</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Noninvasive Ventilation</subject><subject>Original Communication</subject><subject>Oxygen therapy</subject><subject>Patients</subject><subject>Polysomnography</subject><subject>Respiration</subject><subject>Respiratory Insufficiency - etiology</subject><subject>Respiratory Insufficiency - therapy</subject><subject>Retrospective Studies</subject><subject>Sleep</subject><subject>Sleep disorders</subject><subject>Survival</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc2LFDEQxRtR3HH1H_AgAS9eWiufk7kIsugqLAii55BJV89k6e60qfTI_Pdmd9b14-Aph_d7L1X1muY5h9ccYP2GABTXLQjectBGtvCgWXElRcuV3jxsViAVtFpqddY8IboGAFuFx82ZlNaC4XzV5C9Ic8y-pHxks89-xIKZWJpYF_1uSlRiYDQgzozK0kUkNmfsYiiMlnyIBz-wOFVriTgVYj9i2TM_HlPJad5X7-BrYIUoDJgTRXraPOr9QPjs7j1vvn14__XiY3v1-fLTxburNqi1Km1vlek4brZrozqjggnW98bjFjZKcOG55Ur0ttPrvrN8DRp18Mby3qIxnQ_yvHl7yp2X7YhdqOPVOdyc4-jz0SUf3d_KFPdulw7OatASZA14dReQ0_cFqbgxUsBh8BOmhZzQ3Aghpd5U9OU_6HVa8lTXq5QFK7SSN5Q4UaEegjL298NwcDeVulOlrlbqbit1UE0v_lzj3vKrwwrIE0BVmnaYf__9n9ifo8-wBA</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Engel, Markus</creator><creator>Glatz, Christian</creator><creator>Helmle, Cornelia</creator><creator>Young, Peter</creator><creator>Dräger, Bianca</creator><creator>Boentert, Matthias</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7TK</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6133-1397</orcidid></search><sort><creationdate>20211101</creationdate><title>Respiratory parameters on diagnostic sleep studies predict survival in patients with amyotrophic lateral sclerosis</title><author>Engel, Markus ; Glatz, Christian ; Helmle, Cornelia ; Young, Peter ; Dräger, Bianca ; Boentert, Matthias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-f846d1e9b764d64c6c8af6aeb094212a18142f8d57fd81705e5ca681f8e66dac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amyotrophic lateral sclerosis</topic><topic>Amyotrophic Lateral Sclerosis - complications</topic><topic>Amyotrophic Lateral Sclerosis - diagnosis</topic><topic>Amyotrophic Lateral Sclerosis - therapy</topic><topic>Apnea</topic><topic>Blood gas analysis</topic><topic>Carbon dioxide</topic><topic>Female</topic><topic>Humans</topic><topic>Hypercapnia</topic><topic>Mechanical ventilation</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Noninvasive Ventilation</topic><topic>Original Communication</topic><topic>Oxygen therapy</topic><topic>Patients</topic><topic>Polysomnography</topic><topic>Respiration</topic><topic>Respiratory Insufficiency - etiology</topic><topic>Respiratory Insufficiency - therapy</topic><topic>Retrospective Studies</topic><topic>Sleep</topic><topic>Sleep disorders</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Engel, Markus</creatorcontrib><creatorcontrib>Glatz, Christian</creatorcontrib><creatorcontrib>Helmle, Cornelia</creatorcontrib><creatorcontrib>Young, Peter</creatorcontrib><creatorcontrib>Dräger, Bianca</creatorcontrib><creatorcontrib>Boentert, Matthias</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</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>Medical 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 neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Engel, Markus</au><au>Glatz, Christian</au><au>Helmle, Cornelia</au><au>Young, Peter</au><au>Dräger, Bianca</au><au>Boentert, Matthias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Respiratory parameters on diagnostic sleep studies predict survival in patients with amyotrophic lateral sclerosis</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2021-11-01</date><risdate>2021</risdate><volume>268</volume><issue>11</issue><spage>4321</spage><epage>4331</epage><pages>4321-4331</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>Objective
In amyotrophic lateral sclerosis (ALS), respiratory muscle involvement and sleep-disordered breathing relate to worse prognosis. The present study investigated whether respiratory outcomes on first-ever sleep studies predict survival in patients with ALS, specifically taking into account subsequent initiation of non-invasive ventilation (NIV).
Methods
From patients with ALS, baseline sleep study records, transcutaneous capnometry, early morning blood gas analysis, survival data and clinical disease characteristics were retrospectively analyzed. Patients were stratified according to whether enduring NIV was consecutively established (“NIV(+)”) or not (“NIV(–)”).
Results
Among the study cohort (
n
= 158, 72 female, 51 with bulbar onset ALS, 105 deceased) sleep-disordered breathing was present at baseline evaluation in 97 patients. Early morning base excess (EMBE) > 2 mmol/l predicted nocturnal hypercapnia. Ninety-five patients were NIV(+) and 63 were NIV(–). Survival from baseline sleep studies was significantly reduced in NIV(–) but not in NIV(+) patients with nocturnal CO
2
tension ≥ 50 mmHg, apnea hypopnea index ≥ 5/h, and EMBE > 2 mmol/l. Hazard ratio for EMBE > 2 mmol/l was increased in NIV(–) patients only, and EMBE independently predicted survival in both NIV(–) and NIV(+) patients. Furthermore, EMBE on baseline sleep studies was the only predictor for survival from symptom onset, and hazard ratio for shorter survival was markedly higher in the NIV(–) than the NIV(+) group (2.85,
p
= 0.005, vs. 1.71,
p
= 0.042).
Interpretation: In patients with ALS, EMBE > 2 mmol/l predicts nocturnal hypercapnia and shorter survival. Negative effects of sleep-disordered breathing on survival are statistically abolished by sustained NIV.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33880611</pmid><doi>10.1007/s00415-021-10563-0</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-6133-1397</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis - complications Amyotrophic Lateral Sclerosis - diagnosis Amyotrophic Lateral Sclerosis - therapy Apnea Blood gas analysis Carbon dioxide Female Humans Hypercapnia Mechanical ventilation Medical prognosis Medicine Medicine & Public Health Neurology Neuroradiology Neurosciences Noninvasive Ventilation Original Communication Oxygen therapy Patients Polysomnography Respiration Respiratory Insufficiency - etiology Respiratory Insufficiency - therapy Retrospective Studies Sleep Sleep disorders Survival |
title | Respiratory parameters on diagnostic sleep studies predict survival in patients with amyotrophic lateral sclerosis |
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