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Interaction between the genetic variant of rs696217‐ghrelin and food intake and obesity and dyslipidemia
In this study, we aimed to investigate the relationship between the genetic variant of rs696217‐ghrelin and fasted lipid profile, indices of obesity, and environmental parameters. Amplification refractory mutation system‐polymerase chain reaction (ARMs‐PCR) was used for genotyping 1118 individuals r...
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Published in: | Annals of human genetics 2022-01, Vol.86 (1), p.14-23 |
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creator | Yadegari, Mehran Zare‐Feyzabadi, Reza Zakariaeiseraji, Mohanna Sahebi, Reza Shabani, Niloofar Khedmatgozar, Hamed Ferns, Gordon A. Ghazizadeh, Hamideh Mohammadi‐Bajgiran, Maryam Jalalian, Melika Zoghi, Mohadese Darban, Reza Assaran Mohammadian‐Ghosooni, Mahdi Esmaily, Habibollah Avan, Amir Ghayour‐Mobarhan, Majid |
description | In this study, we aimed to investigate the relationship between the genetic variant of rs696217‐ghrelin and fasted lipid profile, indices of obesity, and environmental parameters. Amplification refractory mutation system‐polymerase chain reaction (ARMs‐PCR) was used for genotyping 1118 individuals recruited as part of the Mashhad Stroke and Heart Atherosclerotic Disorder (MASHAD) cohort study. The interaction between the presence of the genetic variant of rs696217‐ghrelin and nutritional intake and other major determinants of obesity and lipid profile was examined in the MASHAD study population. Individuals with the TT genotype at the locus had the lowest prevalence of obesity compared to other genotypes among the individuals. No significant relationship was found between the two groups regarding the lipid profile and TT genotype. Furthermore, no significant association was found between dietary intake and the genetic variant of rs696217‐ghrelin in the population under study. Individuals with a TT or GT genotype appear to be at a higher risk of obesity, compared to those with a GG genotype. The results of the current study revealed a significant association between the genetic variant of rs696217‐ghrelin and obesity; however, this gene did not correlate with the risk factors of cardiovascular diseases and dyslipidemia in the Iranian population. |
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Amplification refractory mutation system‐polymerase chain reaction (ARMs‐PCR) was used for genotyping 1118 individuals recruited as part of the Mashhad Stroke and Heart Atherosclerotic Disorder (MASHAD) cohort study. The interaction between the presence of the genetic variant of rs696217‐ghrelin and nutritional intake and other major determinants of obesity and lipid profile was examined in the MASHAD study population. Individuals with the TT genotype at the locus had the lowest prevalence of obesity compared to other genotypes among the individuals. No significant relationship was found between the two groups regarding the lipid profile and TT genotype. Furthermore, no significant association was found between dietary intake and the genetic variant of rs696217‐ghrelin in the population under study. Individuals with a TT or GT genotype appear to be at a higher risk of obesity, compared to those with a GG genotype. The results of the current study revealed a significant association between the genetic variant of rs696217‐ghrelin and obesity; however, this gene did not correlate with the risk factors of cardiovascular diseases and dyslipidemia in the Iranian population.</description><identifier>ISSN: 0003-4800</identifier><identifier>EISSN: 1469-1809</identifier><identifier>DOI: 10.1111/ahg.12443</identifier><identifier>PMID: 34437712</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Arteriosclerosis ; Cardiovascular diseases ; Cohort Studies ; Dietary intake ; Dyslipidemia ; Dyslipidemias - genetics ; Eating ; Food intake ; Genetic diversity ; Genotype ; Genotype & phenotype ; Genotypes ; Genotyping ; Ghrelin ; Ghrelin - genetics ; Humans ; Iran ; Lipids ; Obesity ; Obesity - genetics ; physical activity ; Polymerase chain reaction ; Polymorphism, Single Nucleotide ; Population studies ; Risk factors</subject><ispartof>Annals of human genetics, 2022-01, Vol.86 (1), p.14-23</ispartof><rights>2021 John Wiley & Sons Ltd/University College London</rights><rights>2021 John Wiley & Sons Ltd/University College London.</rights><rights>2022 John Wiley & Sons Ltd/University College London</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3533-f00e6c54fa9dfc8f5bf9a6009ab1d5119f7a83bdf59bcc57e7d0edf44c3432153</citedby><cites>FETCH-LOGICAL-c3533-f00e6c54fa9dfc8f5bf9a6009ab1d5119f7a83bdf59bcc57e7d0edf44c3432153</cites><orcidid>0000-0002-1081-6754</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34437712$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yadegari, Mehran</creatorcontrib><creatorcontrib>Zare‐Feyzabadi, Reza</creatorcontrib><creatorcontrib>Zakariaeiseraji, Mohanna</creatorcontrib><creatorcontrib>Sahebi, Reza</creatorcontrib><creatorcontrib>Shabani, Niloofar</creatorcontrib><creatorcontrib>Khedmatgozar, Hamed</creatorcontrib><creatorcontrib>Ferns, Gordon A.</creatorcontrib><creatorcontrib>Ghazizadeh, Hamideh</creatorcontrib><creatorcontrib>Mohammadi‐Bajgiran, Maryam</creatorcontrib><creatorcontrib>Jalalian, Melika</creatorcontrib><creatorcontrib>Zoghi, Mohadese</creatorcontrib><creatorcontrib>Darban, Reza Assaran</creatorcontrib><creatorcontrib>Mohammadian‐Ghosooni, Mahdi</creatorcontrib><creatorcontrib>Esmaily, Habibollah</creatorcontrib><creatorcontrib>Avan, Amir</creatorcontrib><creatorcontrib>Ghayour‐Mobarhan, Majid</creatorcontrib><title>Interaction between the genetic variant of rs696217‐ghrelin and food intake and obesity and dyslipidemia</title><title>Annals of human genetics</title><addtitle>Ann Hum Genet</addtitle><description>In this study, we aimed to investigate the relationship between the genetic variant of rs696217‐ghrelin and fasted lipid profile, indices of obesity, and environmental parameters. Amplification refractory mutation system‐polymerase chain reaction (ARMs‐PCR) was used for genotyping 1118 individuals recruited as part of the Mashhad Stroke and Heart Atherosclerotic Disorder (MASHAD) cohort study. The interaction between the presence of the genetic variant of rs696217‐ghrelin and nutritional intake and other major determinants of obesity and lipid profile was examined in the MASHAD study population. Individuals with the TT genotype at the locus had the lowest prevalence of obesity compared to other genotypes among the individuals. No significant relationship was found between the two groups regarding the lipid profile and TT genotype. Furthermore, no significant association was found between dietary intake and the genetic variant of rs696217‐ghrelin in the population under study. Individuals with a TT or GT genotype appear to be at a higher risk of obesity, compared to those with a GG genotype. The results of the current study revealed a significant association between the genetic variant of rs696217‐ghrelin and obesity; however, this gene did not correlate with the risk factors of cardiovascular diseases and dyslipidemia in the Iranian population.</description><subject>Arteriosclerosis</subject><subject>Cardiovascular diseases</subject><subject>Cohort Studies</subject><subject>Dietary intake</subject><subject>Dyslipidemia</subject><subject>Dyslipidemias - genetics</subject><subject>Eating</subject><subject>Food intake</subject><subject>Genetic diversity</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>Ghrelin</subject><subject>Ghrelin - genetics</subject><subject>Humans</subject><subject>Iran</subject><subject>Lipids</subject><subject>Obesity</subject><subject>Obesity - genetics</subject><subject>physical activity</subject><subject>Polymerase chain reaction</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population studies</subject><subject>Risk factors</subject><issn>0003-4800</issn><issn>1469-1809</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kMtOAjEUQBujEUQX_oBp4srFQDvtPLokRIGExI2uJ532ForQwbZI2PkJfqNf4gjqzm5ub3JybnIQuqakT9s3kIt5n6acsxPUpTwXCS2JOEVdQghLeElIB12EsCSEpiVn56jDWrYoaNpFy6mL4KWKtnG4hrgDcDguAM_BQbQKv0lvpYu4MdiHXOQpLT7fP-YLDyvrsHQam6bR2LooX-CwNzUEG_eHv96Hld1YDWsrL9GZkasAVz-zh54f7p9Gk2T2OJ6OhrNEsYyxxBACucq4kUIbVZqsNkLmhAhZU51RKkwhS1Zrk4laqayAQhPQhnPFOEtpxnro9ujd-OZ1CyFWy2brXXuySnPKiBA0S1vq7kgp34TgwVQbb9fS7ytKqu-qVVu1OlRt2Zsf47Zeg_4jfzO2wOAI7OwK9v-bquFkfFR-AV-fgi0</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Yadegari, Mehran</creator><creator>Zare‐Feyzabadi, Reza</creator><creator>Zakariaeiseraji, Mohanna</creator><creator>Sahebi, Reza</creator><creator>Shabani, Niloofar</creator><creator>Khedmatgozar, Hamed</creator><creator>Ferns, Gordon A.</creator><creator>Ghazizadeh, Hamideh</creator><creator>Mohammadi‐Bajgiran, Maryam</creator><creator>Jalalian, Melika</creator><creator>Zoghi, Mohadese</creator><creator>Darban, Reza Assaran</creator><creator>Mohammadian‐Ghosooni, Mahdi</creator><creator>Esmaily, Habibollah</creator><creator>Avan, Amir</creator><creator>Ghayour‐Mobarhan, Majid</creator><general>Wiley Subscription Services, Inc</general><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-1081-6754</orcidid></search><sort><creationdate>202201</creationdate><title>Interaction between the genetic variant of rs696217‐ghrelin and food intake and obesity and dyslipidemia</title><author>Yadegari, Mehran ; Zare‐Feyzabadi, Reza ; Zakariaeiseraji, Mohanna ; Sahebi, Reza ; Shabani, Niloofar ; Khedmatgozar, Hamed ; Ferns, Gordon A. ; Ghazizadeh, Hamideh ; Mohammadi‐Bajgiran, Maryam ; Jalalian, Melika ; Zoghi, Mohadese ; Darban, Reza Assaran ; Mohammadian‐Ghosooni, Mahdi ; Esmaily, Habibollah ; Avan, Amir ; Ghayour‐Mobarhan, Majid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3533-f00e6c54fa9dfc8f5bf9a6009ab1d5119f7a83bdf59bcc57e7d0edf44c3432153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Arteriosclerosis</topic><topic>Cardiovascular diseases</topic><topic>Cohort Studies</topic><topic>Dietary intake</topic><topic>Dyslipidemia</topic><topic>Dyslipidemias - genetics</topic><topic>Eating</topic><topic>Food intake</topic><topic>Genetic diversity</topic><topic>Genotype</topic><topic>Genotype & phenotype</topic><topic>Genotypes</topic><topic>Genotyping</topic><topic>Ghrelin</topic><topic>Ghrelin - genetics</topic><topic>Humans</topic><topic>Iran</topic><topic>Lipids</topic><topic>Obesity</topic><topic>Obesity - genetics</topic><topic>physical activity</topic><topic>Polymerase chain reaction</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Population studies</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yadegari, Mehran</creatorcontrib><creatorcontrib>Zare‐Feyzabadi, Reza</creatorcontrib><creatorcontrib>Zakariaeiseraji, Mohanna</creatorcontrib><creatorcontrib>Sahebi, Reza</creatorcontrib><creatorcontrib>Shabani, Niloofar</creatorcontrib><creatorcontrib>Khedmatgozar, Hamed</creatorcontrib><creatorcontrib>Ferns, Gordon A.</creatorcontrib><creatorcontrib>Ghazizadeh, Hamideh</creatorcontrib><creatorcontrib>Mohammadi‐Bajgiran, Maryam</creatorcontrib><creatorcontrib>Jalalian, Melika</creatorcontrib><creatorcontrib>Zoghi, Mohadese</creatorcontrib><creatorcontrib>Darban, Reza Assaran</creatorcontrib><creatorcontrib>Mohammadian‐Ghosooni, Mahdi</creatorcontrib><creatorcontrib>Esmaily, Habibollah</creatorcontrib><creatorcontrib>Avan, Amir</creatorcontrib><creatorcontrib>Ghayour‐Mobarhan, Majid</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Annals of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yadegari, Mehran</au><au>Zare‐Feyzabadi, Reza</au><au>Zakariaeiseraji, Mohanna</au><au>Sahebi, Reza</au><au>Shabani, Niloofar</au><au>Khedmatgozar, Hamed</au><au>Ferns, Gordon A.</au><au>Ghazizadeh, Hamideh</au><au>Mohammadi‐Bajgiran, Maryam</au><au>Jalalian, Melika</au><au>Zoghi, Mohadese</au><au>Darban, Reza Assaran</au><au>Mohammadian‐Ghosooni, Mahdi</au><au>Esmaily, Habibollah</au><au>Avan, Amir</au><au>Ghayour‐Mobarhan, Majid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction between the genetic variant of rs696217‐ghrelin and food intake and obesity and dyslipidemia</atitle><jtitle>Annals of human genetics</jtitle><addtitle>Ann Hum Genet</addtitle><date>2022-01</date><risdate>2022</risdate><volume>86</volume><issue>1</issue><spage>14</spage><epage>23</epage><pages>14-23</pages><issn>0003-4800</issn><eissn>1469-1809</eissn><abstract>In this study, we aimed to investigate the relationship between the genetic variant of rs696217‐ghrelin and fasted lipid profile, indices of obesity, and environmental parameters. Amplification refractory mutation system‐polymerase chain reaction (ARMs‐PCR) was used for genotyping 1118 individuals recruited as part of the Mashhad Stroke and Heart Atherosclerotic Disorder (MASHAD) cohort study. The interaction between the presence of the genetic variant of rs696217‐ghrelin and nutritional intake and other major determinants of obesity and lipid profile was examined in the MASHAD study population. Individuals with the TT genotype at the locus had the lowest prevalence of obesity compared to other genotypes among the individuals. No significant relationship was found between the two groups regarding the lipid profile and TT genotype. Furthermore, no significant association was found between dietary intake and the genetic variant of rs696217‐ghrelin in the population under study. Individuals with a TT or GT genotype appear to be at a higher risk of obesity, compared to those with a GG genotype. The results of the current study revealed a significant association between the genetic variant of rs696217‐ghrelin and obesity; however, this gene did not correlate with the risk factors of cardiovascular diseases and dyslipidemia in the Iranian population.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34437712</pmid><doi>10.1111/ahg.12443</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1081-6754</orcidid></addata></record> |
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subjects | Arteriosclerosis Cardiovascular diseases Cohort Studies Dietary intake Dyslipidemia Dyslipidemias - genetics Eating Food intake Genetic diversity Genotype Genotype & phenotype Genotypes Genotyping Ghrelin Ghrelin - genetics Humans Iran Lipids Obesity Obesity - genetics physical activity Polymerase chain reaction Polymorphism, Single Nucleotide Population studies Risk factors |
title | Interaction between the genetic variant of rs696217‐ghrelin and food intake and obesity and dyslipidemia |
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