Lean mass and associated factors in women with PCOS with different phenotypes
Although current evidence suggests increased risk of obesity, insulin resistance, and metabolic alterations in patients with polycystic ovary syndrome (PCOS), especially of a hyperandrogenic phenotype, the impact of each one of these variables on muscle mass remains uncertain. In this case-control s...
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description | Although current evidence suggests increased risk of obesity, insulin resistance, and metabolic alterations in patients with polycystic ovary syndrome (PCOS), especially of a hyperandrogenic phenotype, the impact of each one of these variables on muscle mass remains uncertain. In this case-control study, we evaluated clinical and hormonal characteristics related to lean body mass according to the different PCOS phenotypes. We performed clinical, metabolic, and hormonal assessments and evaluated body compartments by dual-energy X-ray absorptiometry in 133 women of reproductive age. Creatinine served as an indirect marker of lean mass. Median age was 28 (range, 17-37) years. Women with phenotypes A and B (n = 59) had higher body mass index (BMI) and metabolic syndrome prevalence than those with phenotype C (n = 23) and controls (n = 51) (p0.005). Women with phenotypes A and B also had higher Ferriman-Gallwey score (p |
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In this case-control study, we evaluated clinical and hormonal characteristics related to lean body mass according to the different PCOS phenotypes. We performed clinical, metabolic, and hormonal assessments and evaluated body compartments by dual-energy X-ray absorptiometry in 133 women of reproductive age. Creatinine served as an indirect marker of lean mass. Median age was 28 (range, 17-37) years. Women with phenotypes A and B (n = 59) had higher body mass index (BMI) and metabolic syndrome prevalence than those with phenotype C (n = 23) and controls (n = 51) (p0.005). Women with phenotypes A and B also had higher Ferriman-Gallwey score (p<0.001), insulin levels (p = 0.006), HOMA-IR (p = 0.008), testosterone (p = 0.008), free androgen index (FAI) (p<0.001), fat mass index (FMI) (p = 0.015), android-to-gynoid fat ratio (p = 0.036), and bone mineral density (BMD) at lumbar spine (p = 0.027) and total femur (p = 0.013) than controls. Median appendicular lean mass index (ALMI) was higher in phenotypes A and B than in controls (7.01 [IQR, 6.33-8.02] vs. 6.69 [IQR, 5.94-7.09], p = 0.024), but it did not differ significantly from that in phenotype C (6.60 [IQR, 6.16-7.22], p = 0.222). Even after adjusting for BMI, ALMI correlated positively with creatinine in women with phenotypes A and B (rho = 0.319, p = 0.023) but not in those with phenotype C (p = 0.238) or controls (p = 0.097). In multivariate linear regression analyses, ALMI was positively associated with insulin, FAI, FMI, and total femur BMD. The present results suggest that fasting insulin, FAI, fat mass, and total femur BMD were positively associated with increased lean mass in women with PCOS phenotypes A and B.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0292623</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Age ; Analysis ; Biology and Life Sciences ; Body composition ; Body fat ; Body mass ; Body mass index ; Body size ; Bone mineral density ; Bones ; Causes of ; Cholesterol ; Complications and side effects ; Creatinine ; Density ; Diagnosis ; Dual energy X-ray absorptiometry ; Femur ; Genetic aspects ; Genotype & phenotype ; Immunoassay ; Insulin ; Insulin resistance ; Lean body mass ; Medicine and Health Sciences ; Metabolic disorders ; Metabolic syndrome ; Morphology ; Obesity ; Overweight ; Phenotype ; Phenotypes ; Polycystic ovary syndrome ; Regression analysis ; Risk factors ; Spine ; Spine (lumbar) ; Statistical analysis ; Stein-Leventhal syndrome ; Testosterone ; Ultrasonic imaging ; Variables ; Variance analysis</subject><ispartof>PloS one, 2023-10, Vol.18 (10), p.e0292623-e0292623</ispartof><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Fighera et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Fighera et al 2023 Fighera et al</rights><rights>2023 Fighera et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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-c670t-fd0008f664cfd6cf6e2e415974d26c862644817a9728335c0ebecc3afecb48963</citedby><cites>FETCH-LOGICAL-c670t-fd0008f664cfd6cf6e2e415974d26c862644817a9728335c0ebecc3afecb48963</cites><orcidid>0000-0002-6734-7688</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/PMC10553224/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553224/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids></links><search><contributor>Yanes Cardozo, Licy</contributor><creatorcontrib>Fighera, Tayane Muniz</creatorcontrib><creatorcontrib>dos Santos, Betânia Rodrigues</creatorcontrib><creatorcontrib>Spritzer, Poli Mara</creatorcontrib><title>Lean mass and associated factors in women with PCOS with different phenotypes</title><title>PloS one</title><description>Although current evidence suggests increased risk of obesity, insulin resistance, and metabolic alterations in patients with polycystic ovary syndrome (PCOS), especially of a hyperandrogenic phenotype, the impact of each one of these variables on muscle mass remains uncertain. In this case-control study, we evaluated clinical and hormonal characteristics related to lean body mass according to the different PCOS phenotypes. We performed clinical, metabolic, and hormonal assessments and evaluated body compartments by dual-energy X-ray absorptiometry in 133 women of reproductive age. Creatinine served as an indirect marker of lean mass. Median age was 28 (range, 17-37) years. Women with phenotypes A and B (n = 59) had higher body mass index (BMI) and metabolic syndrome prevalence than those with phenotype C (n = 23) and controls (n = 51) (p0.005). Women with phenotypes A and B also had higher Ferriman-Gallwey score (p<0.001), insulin levels (p = 0.006), HOMA-IR (p = 0.008), testosterone (p = 0.008), free androgen index (FAI) (p<0.001), fat mass index (FMI) (p = 0.015), android-to-gynoid fat ratio (p = 0.036), and bone mineral density (BMD) at lumbar spine (p = 0.027) and total femur (p = 0.013) than controls. Median appendicular lean mass index (ALMI) was higher in phenotypes A and B than in controls (7.01 [IQR, 6.33-8.02] vs. 6.69 [IQR, 5.94-7.09], p = 0.024), but it did not differ significantly from that in phenotype C (6.60 [IQR, 6.16-7.22], p = 0.222). Even after adjusting for BMI, ALMI correlated positively with creatinine in women with phenotypes A and B (rho = 0.319, p = 0.023) but not in those with phenotype C (p = 0.238) or controls (p = 0.097). In multivariate linear regression analyses, ALMI was positively associated with insulin, FAI, FMI, and total femur BMD. The present results suggest that fasting insulin, FAI, fat mass, and total femur BMD were positively associated with increased lean mass in women with PCOS phenotypes A and B.</description><subject>Age</subject><subject>Analysis</subject><subject>Biology and Life Sciences</subject><subject>Body composition</subject><subject>Body fat</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Body size</subject><subject>Bone mineral density</subject><subject>Bones</subject><subject>Causes of</subject><subject>Cholesterol</subject><subject>Complications and side effects</subject><subject>Creatinine</subject><subject>Density</subject><subject>Diagnosis</subject><subject>Dual energy X-ray absorptiometry</subject><subject>Femur</subject><subject>Genetic aspects</subject><subject>Genotype & phenotype</subject><subject>Immunoassay</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Lean body mass</subject><subject>Medicine and Health Sciences</subject><subject>Metabolic disorders</subject><subject>Metabolic syndrome</subject><subject>Morphology</subject><subject>Obesity</subject><subject>Overweight</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Polycystic ovary syndrome</subject><subject>Regression analysis</subject><subject>Risk factors</subject><subject>Spine</subject><subject>Spine (lumbar)</subject><subject>Statistical analysis</subject><subject>Stein-Leventhal syndrome</subject><subject>Testosterone</subject><subject>Ultrasonic imaging</subject><subject>Variables</subject><subject>Variance 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mass and associated factors in women with PCOS with different phenotypes</title><author>Fighera, Tayane Muniz ; dos Santos, Betânia Rodrigues ; Spritzer, Poli Mara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c670t-fd0008f664cfd6cf6e2e415974d26c862644817a9728335c0ebecc3afecb48963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Age</topic><topic>Analysis</topic><topic>Biology and Life Sciences</topic><topic>Body composition</topic><topic>Body fat</topic><topic>Body mass</topic><topic>Body mass index</topic><topic>Body size</topic><topic>Bone mineral density</topic><topic>Bones</topic><topic>Causes of</topic><topic>Cholesterol</topic><topic>Complications and side effects</topic><topic>Creatinine</topic><topic>Density</topic><topic>Diagnosis</topic><topic>Dual energy X-ray absorptiometry</topic><topic>Femur</topic><topic>Genetic aspects</topic><topic>Genotype & phenotype</topic><topic>Immunoassay</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Lean body mass</topic><topic>Medicine and Health Sciences</topic><topic>Metabolic disorders</topic><topic>Metabolic syndrome</topic><topic>Morphology</topic><topic>Obesity</topic><topic>Overweight</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Polycystic ovary syndrome</topic><topic>Regression analysis</topic><topic>Risk factors</topic><topic>Spine</topic><topic>Spine (lumbar)</topic><topic>Statistical analysis</topic><topic>Stein-Leventhal syndrome</topic><topic>Testosterone</topic><topic>Ultrasonic imaging</topic><topic>Variables</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fighera, Tayane Muniz</creatorcontrib><creatorcontrib>dos Santos, Betânia Rodrigues</creatorcontrib><creatorcontrib>Spritzer, Poli Mara</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: 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one</jtitle><date>2023-10-05</date><risdate>2023</risdate><volume>18</volume><issue>10</issue><spage>e0292623</spage><epage>e0292623</epage><pages>e0292623-e0292623</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Although current evidence suggests increased risk of obesity, insulin resistance, and metabolic alterations in patients with polycystic ovary syndrome (PCOS), especially of a hyperandrogenic phenotype, the impact of each one of these variables on muscle mass remains uncertain. In this case-control study, we evaluated clinical and hormonal characteristics related to lean body mass according to the different PCOS phenotypes. We performed clinical, metabolic, and hormonal assessments and evaluated body compartments by dual-energy X-ray absorptiometry in 133 women of reproductive age. Creatinine served as an indirect marker of lean mass. Median age was 28 (range, 17-37) years. Women with phenotypes A and B (n = 59) had higher body mass index (BMI) and metabolic syndrome prevalence than those with phenotype C (n = 23) and controls (n = 51) (p0.005). Women with phenotypes A and B also had higher Ferriman-Gallwey score (p<0.001), insulin levels (p = 0.006), HOMA-IR (p = 0.008), testosterone (p = 0.008), free androgen index (FAI) (p<0.001), fat mass index (FMI) (p = 0.015), android-to-gynoid fat ratio (p = 0.036), and bone mineral density (BMD) at lumbar spine (p = 0.027) and total femur (p = 0.013) than controls. Median appendicular lean mass index (ALMI) was higher in phenotypes A and B than in controls (7.01 [IQR, 6.33-8.02] vs. 6.69 [IQR, 5.94-7.09], p = 0.024), but it did not differ significantly from that in phenotype C (6.60 [IQR, 6.16-7.22], p = 0.222). Even after adjusting for BMI, ALMI correlated positively with creatinine in women with phenotypes A and B (rho = 0.319, p = 0.023) but not in those with phenotype C (p = 0.238) or controls (p = 0.097). In multivariate linear regression analyses, ALMI was positively associated with insulin, FAI, FMI, and total femur BMD. The present results suggest that fasting insulin, FAI, fat mass, and total femur BMD were positively associated with increased lean mass in women with PCOS phenotypes A and B.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0292623</doi><tpages>e0292623</tpages><orcidid>https://orcid.org/0000-0002-6734-7688</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Analysis Biology and Life Sciences Body composition Body fat Body mass Body mass index Body size Bone mineral density Bones Causes of Cholesterol Complications and side effects Creatinine Density Diagnosis Dual energy X-ray absorptiometry Femur Genetic aspects Genotype & phenotype Immunoassay Insulin Insulin resistance Lean body mass Medicine and Health Sciences Metabolic disorders Metabolic syndrome Morphology Obesity Overweight Phenotype Phenotypes Polycystic ovary syndrome Regression analysis Risk factors Spine Spine (lumbar) Statistical analysis Stein-Leventhal syndrome Testosterone Ultrasonic imaging Variables Variance analysis |
title | Lean mass and associated factors in women with PCOS with different phenotypes |
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