Irisin is a predictor of sarcopenic obesity in type 2 diabetes mellitus: A cross-sectional study
ABSTRACTWe aimed to evaluate sarcopenia and sarcopenic obesity (SO) in patients with type 2 diabetes mellitus (T2DM), possible relationships with serum irisin and myostatin levels, and the effect of glycemic control on SO.Ninety T2DM patients were included in this a cross-sectional study. Sarcopenia...
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Veröffentlicht in: | Medicine (Baltimore) 2021-07, Vol.100 (26), p.e26529-e26529 |
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description | ABSTRACTWe aimed to evaluate sarcopenia and sarcopenic obesity (SO) in patients with type 2 diabetes mellitus (T2DM), possible relationships with serum irisin and myostatin levels, and the effect of glycemic control on SO.Ninety T2DM patients were included in this a cross-sectional study. Sarcopenia was determined by evaluating muscle mass (bioelectrical impedance analysis), muscle strength (HGS), and gait speed (GS). Patients with muscle mass loss with functionally reduced muscle strength and/or performance were considered sarcopenic. In addition, participants were divided into 3 groups according to the FM (fat mass)/FFM (fat-free mass) ratio [group 1:5th-50th percentiles; group 2:50th-95th percentiles and group 3: ≥95 percentiles (sarcopenic obese)]. Irisin, myostatin levels and metabolic parameters were measured in all patients.The prevalence of sarcopenia and SO was 25.6% and 35.6%, respectively. Irisin levels were lower in sarcopenic patients, while glycosylated hemoglobin (A1c), body mass index (BMI), FM, and FM index were higher (P |
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Sarcopenia was determined by evaluating muscle mass (bioelectrical impedance analysis), muscle strength (HGS), and gait speed (GS). Patients with muscle mass loss with functionally reduced muscle strength and/or performance were considered sarcopenic. In addition, participants were divided into 3 groups according to the FM (fat mass)/FFM (fat-free mass) ratio [group 1:5th-50th percentiles; group 2:50th-95th percentiles and group 3: ≥95 percentiles (sarcopenic obese)]. Irisin, myostatin levels and metabolic parameters were measured in all patients.The prevalence of sarcopenia and SO was 25.6% and 35.6%, respectively. Irisin levels were lower in sarcopenic patients, while glycosylated hemoglobin (A1c), body mass index (BMI), FM, and FM index were higher (P < .05). From group 1 to group 3, BMI, FM, FM index, GS, myostatin, and A1c increased, and muscle mass percentage, HGS, and irisin decreased (P < .05). A positive correlation was found between FM/FFM and myostatin and a negative correlation between FM/FFM and irisin (r = 0.303, P = .004 vs. r = -0.491, P < .001). Irisin remained an important predictor of SO, even after adjusting for confounding variables (OR:1.105; 95% CI:0.965-1.338, P = .002). The optimal cut-off value for irisin to predict SO was 9.49 ng/mL (specificity = 78.1%, sensitivity = 75.8%). In addition, A1c was an independent risk factor for SO development (OR:1.358, P = .055).This study showed that low irisin levels (<9.49ng/mL) and poor glycemic control in T2DM patients were an independent risk factor, especially for SO.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000026529</identifier><identifier>PMID: 34190188</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Observational Study</subject><ispartof>Medicine (Baltimore), 2021-07, Vol.100 (26), p.e26529-e26529</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3327-cf77baa7b0bac4ae4f8c219f52a7e7955d2fa08f71fc61f45b1b279e1414fce73</cites><orcidid>0000-0002-9518-8610</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257893/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257893/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Oguz, Ayten</creatorcontrib><creatorcontrib>Sahin, Murat</creatorcontrib><creatorcontrib>Tuzun, Dilek</creatorcontrib><creatorcontrib>Kurutas, Ergul B.</creatorcontrib><creatorcontrib>Ulgen, Cansu</creatorcontrib><creatorcontrib>Bozkus, Ozlem</creatorcontrib><creatorcontrib>Gul, Kamile</creatorcontrib><title>Irisin is a predictor of sarcopenic obesity in type 2 diabetes mellitus: A cross-sectional study</title><title>Medicine (Baltimore)</title><description>ABSTRACTWe aimed to evaluate sarcopenia and sarcopenic obesity (SO) in patients with type 2 diabetes mellitus (T2DM), possible relationships with serum irisin and myostatin levels, and the effect of glycemic control on SO.Ninety T2DM patients were included in this a cross-sectional study. Sarcopenia was determined by evaluating muscle mass (bioelectrical impedance analysis), muscle strength (HGS), and gait speed (GS). Patients with muscle mass loss with functionally reduced muscle strength and/or performance were considered sarcopenic. In addition, participants were divided into 3 groups according to the FM (fat mass)/FFM (fat-free mass) ratio [group 1:5th-50th percentiles; group 2:50th-95th percentiles and group 3: ≥95 percentiles (sarcopenic obese)]. Irisin, myostatin levels and metabolic parameters were measured in all patients.The prevalence of sarcopenia and SO was 25.6% and 35.6%, respectively. Irisin levels were lower in sarcopenic patients, while glycosylated hemoglobin (A1c), body mass index (BMI), FM, and FM index were higher (P < .05). From group 1 to group 3, BMI, FM, FM index, GS, myostatin, and A1c increased, and muscle mass percentage, HGS, and irisin decreased (P < .05). A positive correlation was found between FM/FFM and myostatin and a negative correlation between FM/FFM and irisin (r = 0.303, P = .004 vs. r = -0.491, P < .001). Irisin remained an important predictor of SO, even after adjusting for confounding variables (OR:1.105; 95% CI:0.965-1.338, P = .002). The optimal cut-off value for irisin to predict SO was 9.49 ng/mL (specificity = 78.1%, sensitivity = 75.8%). In addition, A1c was an independent risk factor for SO development (OR:1.358, P = .055).This study showed that low irisin levels (<9.49ng/mL) and poor glycemic control in T2DM patients were an independent risk factor, especially for SO.</description><subject>Observational Study</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdUU1v1TAQtBCIPgq_gIuPXFL8mY05IFUtH5Va9VLOxnHWPENeHGyn1fv3hL4K1O5lpdmZWY2GkLecnXBm4P3V-Qn7P6LVwjwjG65l22jTqudks6K6AQPqiLwq5SdjXIJQL8mRVNww3nUb8v0ixxInGgt1dM44RF9TpinQ4rJPM07R09RjiXVPV17dz0gFHaLrsWKhOxzHWJfygZ5Sn1MpTUFfY5rcSEtdhv1r8iK4seCbh31Mvn3-dHP2tbm8_nJxdnrZeCkFND4A9M5Bz3rnlUMVOi-4CVo4QDBaDyI41gXgwbc8KN3zXoBBrrgKHkEek48H33npdzh4nGp2o51z3Lm8t8lF-_gyxa39kW5tJzR0Rq4G7x4Mcvq9YKl2F4tf47kJ01Ks0Ko1oEGIlSoP1PvEGcO_N5zZv93Yq3P7tJtVpQ6quzRWzOXXuNxhtlt0Y93e0zUY0QgmOAMmWLMiCuQf7HCRzA</recordid><startdate>20210702</startdate><enddate>20210702</enddate><creator>Oguz, Ayten</creator><creator>Sahin, Murat</creator><creator>Tuzun, Dilek</creator><creator>Kurutas, Ergul B.</creator><creator>Ulgen, Cansu</creator><creator>Bozkus, Ozlem</creator><creator>Gul, Kamile</creator><general>Lippincott Williams & Wilkins</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9518-8610</orcidid></search><sort><creationdate>20210702</creationdate><title>Irisin is a predictor of sarcopenic obesity in type 2 diabetes mellitus: A cross-sectional study</title><author>Oguz, Ayten ; Sahin, Murat ; Tuzun, Dilek ; Kurutas, Ergul B. ; Ulgen, Cansu ; Bozkus, Ozlem ; Gul, Kamile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3327-cf77baa7b0bac4ae4f8c219f52a7e7955d2fa08f71fc61f45b1b279e1414fce73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Observational Study</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oguz, Ayten</creatorcontrib><creatorcontrib>Sahin, Murat</creatorcontrib><creatorcontrib>Tuzun, Dilek</creatorcontrib><creatorcontrib>Kurutas, Ergul B.</creatorcontrib><creatorcontrib>Ulgen, Cansu</creatorcontrib><creatorcontrib>Bozkus, Ozlem</creatorcontrib><creatorcontrib>Gul, Kamile</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oguz, Ayten</au><au>Sahin, Murat</au><au>Tuzun, Dilek</au><au>Kurutas, Ergul B.</au><au>Ulgen, Cansu</au><au>Bozkus, Ozlem</au><au>Gul, Kamile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Irisin is a predictor of sarcopenic obesity in type 2 diabetes mellitus: A cross-sectional study</atitle><jtitle>Medicine (Baltimore)</jtitle><date>2021-07-02</date><risdate>2021</risdate><volume>100</volume><issue>26</issue><spage>e26529</spage><epage>e26529</epage><pages>e26529-e26529</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>ABSTRACTWe aimed to evaluate sarcopenia and sarcopenic obesity (SO) in patients with type 2 diabetes mellitus (T2DM), possible relationships with serum irisin and myostatin levels, and the effect of glycemic control on SO.Ninety T2DM patients were included in this a cross-sectional study. Sarcopenia was determined by evaluating muscle mass (bioelectrical impedance analysis), muscle strength (HGS), and gait speed (GS). Patients with muscle mass loss with functionally reduced muscle strength and/or performance were considered sarcopenic. In addition, participants were divided into 3 groups according to the FM (fat mass)/FFM (fat-free mass) ratio [group 1:5th-50th percentiles; group 2:50th-95th percentiles and group 3: ≥95 percentiles (sarcopenic obese)]. Irisin, myostatin levels and metabolic parameters were measured in all patients.The prevalence of sarcopenia and SO was 25.6% and 35.6%, respectively. Irisin levels were lower in sarcopenic patients, while glycosylated hemoglobin (A1c), body mass index (BMI), FM, and FM index were higher (P < .05). From group 1 to group 3, BMI, FM, FM index, GS, myostatin, and A1c increased, and muscle mass percentage, HGS, and irisin decreased (P < .05). A positive correlation was found between FM/FFM and myostatin and a negative correlation between FM/FFM and irisin (r = 0.303, P = .004 vs. r = -0.491, P < .001). Irisin remained an important predictor of SO, even after adjusting for confounding variables (OR:1.105; 95% CI:0.965-1.338, P = .002). The optimal cut-off value for irisin to predict SO was 9.49 ng/mL (specificity = 78.1%, sensitivity = 75.8%). In addition, A1c was an independent risk factor for SO development (OR:1.358, P = .055).This study showed that low irisin levels (<9.49ng/mL) and poor glycemic control in T2DM patients were an independent risk factor, especially for SO.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>34190188</pmid><doi>10.1097/MD.0000000000026529</doi><orcidid>https://orcid.org/0000-0002-9518-8610</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Observational Study |
title | Irisin is a predictor of sarcopenic obesity in type 2 diabetes mellitus: A cross-sectional study |
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