Dysphagia in duchenne muscular dystrophy versus myotonic dystrophy type 1
Introduction: In this study we aimed to demonstrate the distinctive features of dysphagia in patients with myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD). Methods: Diet‐type score (DTS) and maximum tongue pressure (MTP) were measured in 20 DM1 and 24 DMD patients; all patients...
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| Veröffentlicht in: | Muscle & nerve 2012-10, Vol.46 (4), p.490-495 |
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| container_title | Muscle & nerve |
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| creator | Umemoto, George Furuya, Hirokazu Kitashima, Akio Sakai, Mitsuaki Arahata, Hajime Kikuta, Toshihiro |
| description | Introduction:
In this study we aimed to demonstrate the distinctive features of dysphagia in patients with myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD).
Methods:
Diet‐type score (DTS) and maximum tongue pressure (MTP) were measured in 20 DM1 and 24 DMD patients; all patients were also examined by videofluoroscopy (VF). We used VF to measure the range of hyoid bone excursion (RHBE) during pharyngeal transit time and the area of pharyngeal residue (APR) after the first swallow.
Results:
RHBE and APR values for DM1 patients were significantly greater than those for DMD patients. DTS and MTP did not differ between patients. A significant correlation was observed between DTS, MTP, and RHBE in DMD patients, but not in DM1 patients.
Conclusions:
Our findings reveal the differences in the distinctive features of dysphagia in DM1 and DMD. Adjustments in the diet of DMD patients in accordance with swallowing ability could be useful. Muscle Nerve 46: 490–495, 2012 |
| doi_str_mv | 10.1002/mus.23364 |
| format | Article |
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In this study we aimed to demonstrate the distinctive features of dysphagia in patients with myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD).
Methods:
Diet‐type score (DTS) and maximum tongue pressure (MTP) were measured in 20 DM1 and 24 DMD patients; all patients were also examined by videofluoroscopy (VF). We used VF to measure the range of hyoid bone excursion (RHBE) during pharyngeal transit time and the area of pharyngeal residue (APR) after the first swallow.
Results:
RHBE and APR values for DM1 patients were significantly greater than those for DMD patients. DTS and MTP did not differ between patients. A significant correlation was observed between DTS, MTP, and RHBE in DMD patients, but not in DM1 patients.
Conclusions:
Our findings reveal the differences in the distinctive features of dysphagia in DM1 and DMD. Adjustments in the diet of DMD patients in accordance with swallowing ability could be useful. Muscle Nerve 46: 490–495, 2012</description><identifier>ISSN: 0148-639X</identifier><identifier>EISSN: 1097-4598</identifier><identifier>DOI: 10.1002/mus.23364</identifier><identifier>PMID: 22987688</identifier><identifier>CODEN: MUNEDE</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Biological and medical sciences ; Deglutition Disorders - diagnostic imaging ; Deglutition Disorders - etiology ; Deglutition Disorders - physiopathology ; Diseases of striated muscles. Neuromuscular diseases ; Duchenne muscular dystrophy ; Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology ; Female ; Humans ; hyoid bone excursion ; Male ; Medical sciences ; Middle Aged ; Muscular Dystrophy, Duchenne - complications ; Muscular Dystrophy, Duchenne - physiopathology ; Myotonic Dystrophy - complications ; Myotonic Dystrophy - physiopathology ; myotonic dystrophy type 1 ; Neurology ; Non tumoral diseases ; Otorhinolaryngology. Stomatology ; pharyngeal residue ; Radiography ; tongue pressure ; Young Adult</subject><ispartof>Muscle & nerve, 2012-10, Vol.46 (4), p.490-495</ispartof><rights>Copyright © 2012 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4594-27aaf940e90a6dc3c9182b7d06159aaefa33e068634a9cb8b66eca84e3f78f303</citedby><cites>FETCH-LOGICAL-c4594-27aaf940e90a6dc3c9182b7d06159aaefa33e068634a9cb8b66eca84e3f78f303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmus.23364$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmus.23364$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26407384$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22987688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Umemoto, George</creatorcontrib><creatorcontrib>Furuya, Hirokazu</creatorcontrib><creatorcontrib>Kitashima, Akio</creatorcontrib><creatorcontrib>Sakai, Mitsuaki</creatorcontrib><creatorcontrib>Arahata, Hajime</creatorcontrib><creatorcontrib>Kikuta, Toshihiro</creatorcontrib><title>Dysphagia in duchenne muscular dystrophy versus myotonic dystrophy type 1</title><title>Muscle & nerve</title><addtitle>Muscle Nerve</addtitle><description>Introduction:
In this study we aimed to demonstrate the distinctive features of dysphagia in patients with myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD).
Methods:
Diet‐type score (DTS) and maximum tongue pressure (MTP) were measured in 20 DM1 and 24 DMD patients; all patients were also examined by videofluoroscopy (VF). We used VF to measure the range of hyoid bone excursion (RHBE) during pharyngeal transit time and the area of pharyngeal residue (APR) after the first swallow.
Results:
RHBE and APR values for DM1 patients were significantly greater than those for DMD patients. DTS and MTP did not differ between patients. A significant correlation was observed between DTS, MTP, and RHBE in DMD patients, but not in DM1 patients.
Conclusions:
Our findings reveal the differences in the distinctive features of dysphagia in DM1 and DMD. Adjustments in the diet of DMD patients in accordance with swallowing ability could be useful. Muscle Nerve 46: 490–495, 2012</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Deglutition Disorders - diagnostic imaging</subject><subject>Deglutition Disorders - etiology</subject><subject>Deglutition Disorders - physiopathology</subject><subject>Diseases of striated muscles. Neuromuscular diseases</subject><subject>Duchenne muscular dystrophy</subject><subject>Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology</subject><subject>Female</subject><subject>Humans</subject><subject>hyoid bone excursion</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Muscular Dystrophy, Duchenne - complications</subject><subject>Muscular Dystrophy, Duchenne - physiopathology</subject><subject>Myotonic Dystrophy - complications</subject><subject>Myotonic Dystrophy - physiopathology</subject><subject>myotonic dystrophy type 1</subject><subject>Neurology</subject><subject>Non tumoral diseases</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>pharyngeal residue</subject><subject>Radiography</subject><subject>tongue pressure</subject><subject>Young Adult</subject><issn>0148-639X</issn><issn>1097-4598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MlS3DAQBmAVRSoMJAdegPKFqnAwI1kaLceEsEyYJFUJ203VI7cZJ96QbMBvj2GG5cJJB339t_QTss3oPqM0GZdd2E84l2KNjBg1KhYTo9fJiDKhY8nN1QbZDOEfpZRpqT6SjSQxWkmtR2T6vQ_NAq5ziPIqSju3wKrCaEh0XQE-SvvQ-rpZ9NEt-tCFqOzrtq5y9-am7RuM2CfyIYMi4OfVuUXOjw7PDk7i2e_j6cHXWeyGV4k4UQCZERQNBZk67gzTyVylVLKJAcAMOEcqteQCjJvruZToQAvkmdIZp3yLfFnmNr6-6TC0tsyDw6KACusuWEYFY4KZRA50b0mdr0PwmNnG5yX4fkD2sTk7_NM-NTfYnVVsNy8xfZHPVQ1gdwUgOCgyD5XLw6uTgiquH4PGS3eXF9i_v9H-PP_7vDpeTuShxfuXCfD_rVRcTezlr2N7evrtx8WfmbET_gAC6JUB</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Umemoto, George</creator><creator>Furuya, Hirokazu</creator><creator>Kitashima, Akio</creator><creator>Sakai, Mitsuaki</creator><creator>Arahata, Hajime</creator><creator>Kikuta, Toshihiro</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>201210</creationdate><title>Dysphagia in duchenne muscular dystrophy versus myotonic dystrophy type 1</title><author>Umemoto, George ; Furuya, Hirokazu ; Kitashima, Akio ; Sakai, Mitsuaki ; Arahata, Hajime ; Kikuta, Toshihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4594-27aaf940e90a6dc3c9182b7d06159aaefa33e068634a9cb8b66eca84e3f78f303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Deglutition Disorders - diagnostic imaging</topic><topic>Deglutition Disorders - etiology</topic><topic>Deglutition Disorders - physiopathology</topic><topic>Diseases of striated muscles. Neuromuscular diseases</topic><topic>Duchenne muscular dystrophy</topic><topic>Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology</topic><topic>Female</topic><topic>Humans</topic><topic>hyoid bone excursion</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscular Dystrophy, Duchenne - complications</topic><topic>Muscular Dystrophy, Duchenne - physiopathology</topic><topic>Myotonic Dystrophy - complications</topic><topic>Myotonic Dystrophy - physiopathology</topic><topic>myotonic dystrophy type 1</topic><topic>Neurology</topic><topic>Non tumoral diseases</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>pharyngeal residue</topic><topic>Radiography</topic><topic>tongue pressure</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Umemoto, George</creatorcontrib><creatorcontrib>Furuya, Hirokazu</creatorcontrib><creatorcontrib>Kitashima, Akio</creatorcontrib><creatorcontrib>Sakai, Mitsuaki</creatorcontrib><creatorcontrib>Arahata, Hajime</creatorcontrib><creatorcontrib>Kikuta, Toshihiro</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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><jtitle>Muscle & nerve</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Umemoto, George</au><au>Furuya, Hirokazu</au><au>Kitashima, Akio</au><au>Sakai, Mitsuaki</au><au>Arahata, Hajime</au><au>Kikuta, Toshihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dysphagia in duchenne muscular dystrophy versus myotonic dystrophy type 1</atitle><jtitle>Muscle & nerve</jtitle><addtitle>Muscle Nerve</addtitle><date>2012-10</date><risdate>2012</risdate><volume>46</volume><issue>4</issue><spage>490</spage><epage>495</epage><pages>490-495</pages><issn>0148-639X</issn><eissn>1097-4598</eissn><coden>MUNEDE</coden><abstract>Introduction:
In this study we aimed to demonstrate the distinctive features of dysphagia in patients with myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD).
Methods:
Diet‐type score (DTS) and maximum tongue pressure (MTP) were measured in 20 DM1 and 24 DMD patients; all patients were also examined by videofluoroscopy (VF). We used VF to measure the range of hyoid bone excursion (RHBE) during pharyngeal transit time and the area of pharyngeal residue (APR) after the first swallow.
Results:
RHBE and APR values for DM1 patients were significantly greater than those for DMD patients. DTS and MTP did not differ between patients. A significant correlation was observed between DTS, MTP, and RHBE in DMD patients, but not in DM1 patients.
Conclusions:
Our findings reveal the differences in the distinctive features of dysphagia in DM1 and DMD. Adjustments in the diet of DMD patients in accordance with swallowing ability could be useful. Muscle Nerve 46: 490–495, 2012</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22987688</pmid><doi>10.1002/mus.23364</doi><tpages>6</tpages></addata></record> |
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| subjects | Adult Biological and medical sciences Deglutition Disorders - diagnostic imaging Deglutition Disorders - etiology Deglutition Disorders - physiopathology Diseases of striated muscles. Neuromuscular diseases Duchenne muscular dystrophy Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology Female Humans hyoid bone excursion Male Medical sciences Middle Aged Muscular Dystrophy, Duchenne - complications Muscular Dystrophy, Duchenne - physiopathology Myotonic Dystrophy - complications Myotonic Dystrophy - physiopathology myotonic dystrophy type 1 Neurology Non tumoral diseases Otorhinolaryngology. Stomatology pharyngeal residue Radiography tongue pressure Young Adult |
| title | Dysphagia in duchenne muscular dystrophy versus myotonic dystrophy type 1 |
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