Effects of Polycystic Ovary Syndrome (PCOS), Sex Hormones, and Obesity on Circulating miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 Expression
Context:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycysti...
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Published in | The journal of clinical endocrinology and metabolism Vol. 98; no. 11; pp. E1835 - E1844 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Oxford University Press
01.11.2013
Copyright by The Endocrine Society |
Subjects | |
Online Access | Get full text |
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Abstract | Context:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS).Objective:We aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs.Design:This was a case-control study.Settings:The setting was an academic hospital.Participants:We included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m2), and six subjects per group were obese (BMI ≥ 30 kg/m2).Interventions:Blood samples were collected early in the morning after a 12-hour fast.Main Outcome Measures:We measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155.Results:Obesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations.Conclusions:The present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations. |
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AbstractList | MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS).
We aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs.
This was a case-control study.
The setting was an academic hospital.
We included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m(2)), and six subjects per group were obese (BMI ≥ 30 kg/m(2)).
Blood samples were collected early in the morning after a 12-hour fast.
We measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155.
Obesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations.
The present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations. Context:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS).Objective:We aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs.Design:This was a case-control study.Settings:The setting was an academic hospital.Participants:We included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m2), and six subjects per group were obese (BMI greater than or equal to 30 kg/m2).Interventions:Blood samples were collected early in the morning after a 12-hour fast.Main Outcome Measures:We measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155.Results:Obesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations.Conclusions:The present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations. CONTEXT:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS). OBJECTIVE:We aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs. DESIGN:This was a case-control study. SETTINGS:The setting was an academic hospital. PARTICIPANTS:We included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m), and six subjects per group were obese (BMI ≥ 30 kg/m). INTERVENTIONS:Blood samples were collected early in the morning after a 12-hour fast. MAIN OUTCOME MEASURES:We measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155. RESULTS:Obesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations. CONCLUSIONS:The present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations. MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS).CONTEXTMicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS).We aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs.OBJECTIVEWe aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs.This was a case-control study.DESIGNThis was a case-control study.The setting was an academic hospital.SETTINGSThe setting was an academic hospital.We included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m(2)), and six subjects per group were obese (BMI ≥ 30 kg/m(2)).PARTICIPANTSWe included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m(2)), and six subjects per group were obese (BMI ≥ 30 kg/m(2)).Blood samples were collected early in the morning after a 12-hour fast.INTERVENTIONSBlood samples were collected early in the morning after a 12-hour fast.We measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155.MAIN OUTCOME MEASURESWe measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155.Obesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations.RESULTSObesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations.The present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations.CONCLUSIONSThe present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations. Context:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 have been associated with metabolic disorders such as obesity and diabetes, which are also associated with polycystic ovary syndrome (PCOS).Objective:We aimed to evaluate the effects of sex, sex hormones, and PCOS and their interactions with obesity on the expression in the circulation of these miRNAs.Design:This was a case-control study.Settings:The setting was an academic hospital.Participants:We included 12 control women, 12 patients with PCOS, and 12 men selected as to have similar body mass index (BMI) and age. Six subjects per group had normal weight (BMI < 25 kg/m2), and six subjects per group were obese (BMI ≥ 30 kg/m2).Interventions:Blood samples were collected early in the morning after a 12-hour fast.Main Outcome Measures:We measured whole blood expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155.Results:Obesity significantly reduced the expression of miRNA-21, miRNA-27b, and miRNA-103. However, there was a significant interaction between obesity and the group of subjects in the expression of miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 consisting of obesity reducing the expression of these miRNAs in control woman and men, but tending to increase their expression in women with PCOS. These differences paralleled those observed in serum T concentrations.Conclusions:The present results suggest that miRNAs that play an important role in metabolic and immune system processes are influenced by obesity and circulating androgen concentrations. |
Author | Fernández-Durán, Elena Murri, Mora Escobar-Morreale, Héctor F. Insenser, María San-Millán, José L. |
AuthorAffiliation | Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain |
AuthorAffiliation_xml | – name: Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain |
Author_xml | – sequence: 1 givenname: Mora surname: Murri fullname: Murri, Mora email: moramurri@gmail.com organization: 1Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain – sequence: 2 givenname: María surname: Insenser fullname: Insenser, María organization: 1Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain – sequence: 3 givenname: Elena surname: Fernández-Durán fullname: Fernández-Durán, Elena organization: 1Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain – sequence: 4 givenname: José L. surname: San-Millán fullname: San-Millán, José L. organization: 1Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain – sequence: 5 givenname: Héctor F. surname: Escobar-Morreale fullname: Escobar-Morreale, Héctor F. email: hectorfrancisco.escobar@salud.madrid.org organization: 1Diabetes, Obesity, and Human Reproduction Research Group; Hospital Universitario Ramón y Cajal and Universidad de Alcalá; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS); and Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), E-28034 Madrid, Spain |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24037889$$D View this record in MEDLINE/PubMed |
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Snippet | Context:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b,... CONTEXT:MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b,... MicroRNAs (miRNAs) are small, noncoding RNA sequences that negatively regulate gene expression at the post-transcriptional level. miRNA-21, miRNA-27b,... |
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SubjectTerms | Adult Body mass index Case-Control Studies Diabetes mellitus Female Gene expression Gene Expression - physiology Gonadal Steroid Hormones - blood Humans Immune system Male Metabolic disorders Metabolism MicroRNAs MicroRNAs - blood MicroRNAs - genetics miRNA Obesity Obesity - genetics Obesity - metabolism Ovaries Polycystic ovary syndrome Polycystic Ovary Syndrome - genetics Polycystic Ovary Syndrome - metabolism Post-transcription Sex hormones Young Adult |
Title | Effects of Polycystic Ovary Syndrome (PCOS), Sex Hormones, and Obesity on Circulating miRNA-21, miRNA-27b, miRNA-103, and miRNA-155 Expression |
URI | https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00004678-201311000-00067 https://www.ncbi.nlm.nih.gov/pubmed/24037889 https://www.proquest.com/docview/3164451991 https://www.proquest.com/docview/1449277332 https://www.proquest.com/docview/1551639068 |
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