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
Hauptverfasser: Oguz, Ayten, Sahin, Murat, Tuzun, Dilek, Kurutas, Ergul B., Ulgen, Cansu, Bozkus, Ozlem, Gul, Kamile
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container_title Medicine (Baltimore)
container_volume 100
creator Oguz, Ayten
Sahin, Murat
Tuzun, Dilek
Kurutas, Ergul B.
Ulgen, Cansu
Bozkus, Ozlem
Gul, Kamile
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 &lt; .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 &lt; .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 &lt; .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 (&lt;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 &amp; Wilkins</publisher><subject>Observational Study</subject><ispartof>Medicine (Baltimore), 2021-07, Vol.100 (26), p.e26529-e26529</ispartof><rights>Lippincott Williams &amp; Wilkins</rights><rights>Copyright © 2021 the Author(s). 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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 &lt; .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 &lt; .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 &lt; .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 (&lt;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 &amp; 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 &lt; .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 &lt; .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 &lt; .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 (&lt;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 &amp; 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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title Irisin is a predictor of sarcopenic obesity in type 2 diabetes mellitus: A cross-sectional study
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