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Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence
Males have greater cardiometabolic risk than females, though the reasons for this are poorly understood. The aim of this study was to examine the association between common Y chromosomal haplogroups and cardiometabolic risk during early life. In a British birth cohort, we examined the association of...
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Published in: | Atherosclerosis 2018-07, Vol.274, p.94-103 |
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creator | O'Keeffe, Linda M. Howe, Laura D. Fraser, Abigail Hughes, Alun D. Wade, Kaitlin H. Anderson, Emma L. Lawlor, Debbie A. Erzurumluoglu, A. Mesut Davey-Smith, George Rodriguez, Santiago Stergiakouli, Evie |
description | Males have greater cardiometabolic risk than females, though the reasons for this are poorly understood. The aim of this study was to examine the association between common Y chromosomal haplogroups and cardiometabolic risk during early life.
In a British birth cohort, we examined the association of Y chromosomal haplogroups with trajectories of cardiometabolic risk factors from birth to 18 years and with carotid-femoral pulse wave velocity, carotid intima media thickness and left ventricular mass index at age 18. Haplogroups were grouped according to their phylogenetic relatedness into categories of R, I, E, J, G and all other haplogroups combined (T, Q, H, L, C, N and O). Risk factors included BMI, fat and lean mass, systolic blood pressure (SBP), diastolic blood pressure, pulse rate, triglycerides, high density lipoprotein cholesterol (HDL-c), non-HDL-c and c-reactive protein. Analyses were performed using multilevel models and linear regression, as appropriate.
Y chromosomal haplogroups were not associated with any cardiometabolic risk factors from birth to 18 years. For example, at age 18, the difference in SBP comparing each haplogroup with haplogroup R was −0.39 mmHg (95% Confidence Interval (CI): −0.75, 1.54) for haplogroup I, 2.56 mmHg (95% CI: −0.76, 5.89) for haplogroup E, −0.02 mmHg (95% CI: −2.87, 2.83) for haplogroup J, 1.28 mmHg (95% CI: −4.70, 2.13) for haplogroup G and −2.75 mmHg (95% CI: −6.38, 0.88) for all other haplogroups combined.
Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors during childhood and adolescence or with subclinical cardiovascular measures at age 18.
•Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors from birth to age 18.•Common Y chromosomal haplogroups are not associated with cardiovascular structure and function at age 18.•Common Y chromosomal haplogroups are not associated with cardiometabolic risk in males during early life. |
doi_str_mv | 10.1016/j.atherosclerosis.2018.04.027 |
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In a British birth cohort, we examined the association of Y chromosomal haplogroups with trajectories of cardiometabolic risk factors from birth to 18 years and with carotid-femoral pulse wave velocity, carotid intima media thickness and left ventricular mass index at age 18. Haplogroups were grouped according to their phylogenetic relatedness into categories of R, I, E, J, G and all other haplogroups combined (T, Q, H, L, C, N and O). Risk factors included BMI, fat and lean mass, systolic blood pressure (SBP), diastolic blood pressure, pulse rate, triglycerides, high density lipoprotein cholesterol (HDL-c), non-HDL-c and c-reactive protein. Analyses were performed using multilevel models and linear regression, as appropriate.
Y chromosomal haplogroups were not associated with any cardiometabolic risk factors from birth to 18 years. For example, at age 18, the difference in SBP comparing each haplogroup with haplogroup R was −0.39 mmHg (95% Confidence Interval (CI): −0.75, 1.54) for haplogroup I, 2.56 mmHg (95% CI: −0.76, 5.89) for haplogroup E, −0.02 mmHg (95% CI: −2.87, 2.83) for haplogroup J, 1.28 mmHg (95% CI: −4.70, 2.13) for haplogroup G and −2.75 mmHg (95% CI: −6.38, 0.88) for all other haplogroups combined.
Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors during childhood and adolescence or with subclinical cardiovascular measures at age 18.
•Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors from birth to age 18.•Common Y chromosomal haplogroups are not associated with cardiovascular structure and function at age 18.•Common Y chromosomal haplogroups are not associated with cardiometabolic risk in males during early life.</description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/j.atherosclerosis.2018.04.027</identifier><identifier>PMID: 29753233</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Adolescence ; Adolescent ; Age Factors ; Asymptomatic Diseases ; Cardiometabolic ; Cardiovascular Diseases - diagnosis ; Cardiovascular Diseases - epidemiology ; Cardiovascular Diseases - genetics ; Child ; Child, Preschool ; Childhood ; Chromosomes, Human, Y - genetics ; England - epidemiology ; Genetic Predisposition to Disease ; Haplotypes ; Health Status ; Humans ; Infant ; Infant, Newborn ; Longitudinal Studies ; Male ; Metabolic Syndrome - diagnosis ; Metabolic Syndrome - epidemiology ; Metabolic Syndrome - genetics ; Phenotype ; Prognosis ; Prospective Studies ; Risk Assessment ; Risk Factors ; Sex Factors ; Time Factors ; Vascular ; Y chromosome</subject><ispartof>Atherosclerosis, 2018-07, Vol.274, p.94-103</ispartof><rights>2018 The Authors</rights><rights>Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.</rights><rights>2018 The Authors 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-6e276217e9d19f9b3614bde412ea947a56ea2a9919980e358ec54e6cf86dd7cb3</citedby><cites>FETCH-LOGICAL-c499t-6e276217e9d19f9b3614bde412ea947a56ea2a9919980e358ec54e6cf86dd7cb3</cites><orcidid>0000-0002-0003-0774 ; 0000-0002-7741-9470 ; 0000-0003-1322-8138</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29753233$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Keeffe, Linda M.</creatorcontrib><creatorcontrib>Howe, Laura D.</creatorcontrib><creatorcontrib>Fraser, Abigail</creatorcontrib><creatorcontrib>Hughes, Alun D.</creatorcontrib><creatorcontrib>Wade, Kaitlin H.</creatorcontrib><creatorcontrib>Anderson, Emma L.</creatorcontrib><creatorcontrib>Lawlor, Debbie A.</creatorcontrib><creatorcontrib>Erzurumluoglu, A. Mesut</creatorcontrib><creatorcontrib>Davey-Smith, George</creatorcontrib><creatorcontrib>Rodriguez, Santiago</creatorcontrib><creatorcontrib>Stergiakouli, Evie</creatorcontrib><title>Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>Males have greater cardiometabolic risk than females, though the reasons for this are poorly understood. The aim of this study was to examine the association between common Y chromosomal haplogroups and cardiometabolic risk during early life.
In a British birth cohort, we examined the association of Y chromosomal haplogroups with trajectories of cardiometabolic risk factors from birth to 18 years and with carotid-femoral pulse wave velocity, carotid intima media thickness and left ventricular mass index at age 18. Haplogroups were grouped according to their phylogenetic relatedness into categories of R, I, E, J, G and all other haplogroups combined (T, Q, H, L, C, N and O). Risk factors included BMI, fat and lean mass, systolic blood pressure (SBP), diastolic blood pressure, pulse rate, triglycerides, high density lipoprotein cholesterol (HDL-c), non-HDL-c and c-reactive protein. Analyses were performed using multilevel models and linear regression, as appropriate.
Y chromosomal haplogroups were not associated with any cardiometabolic risk factors from birth to 18 years. For example, at age 18, the difference in SBP comparing each haplogroup with haplogroup R was −0.39 mmHg (95% Confidence Interval (CI): −0.75, 1.54) for haplogroup I, 2.56 mmHg (95% CI: −0.76, 5.89) for haplogroup E, −0.02 mmHg (95% CI: −2.87, 2.83) for haplogroup J, 1.28 mmHg (95% CI: −4.70, 2.13) for haplogroup G and −2.75 mmHg (95% CI: −6.38, 0.88) for all other haplogroups combined.
Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors during childhood and adolescence or with subclinical cardiovascular measures at age 18.
•Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors from birth to age 18.•Common Y chromosomal haplogroups are not associated with cardiovascular structure and function at age 18.•Common Y chromosomal haplogroups are not associated with cardiometabolic risk in males during early life.</description><subject>Adolescence</subject><subject>Adolescent</subject><subject>Age Factors</subject><subject>Asymptomatic Diseases</subject><subject>Cardiometabolic</subject><subject>Cardiovascular Diseases - diagnosis</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - genetics</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Childhood</subject><subject>Chromosomes, Human, Y - genetics</subject><subject>England - epidemiology</subject><subject>Genetic Predisposition to Disease</subject><subject>Haplotypes</subject><subject>Health Status</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Metabolic Syndrome - diagnosis</subject><subject>Metabolic Syndrome - epidemiology</subject><subject>Metabolic Syndrome - genetics</subject><subject>Phenotype</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><subject>Time Factors</subject><subject>Vascular</subject><subject>Y chromosome</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqNkU2P1CAYxxujcWdXv4LhYuKlFSil5aDJZuOuJpt40YMn8hSeThlpGaGdjZ_EryvjrBv15AVInv8L8CuKl4xWjDL5elfBMmIMyfjj6lLFKesqKirK20fFhnWtKpnoxONiQylnpWINPSvOU9pRSkXLuqfFGVdtU_O63hQ_LlMKxsHiwpxIGMgXYsYYppDCBJ6MsPdhG8O6T-TOLSMxEK0LEy7QB-8MiS59JQOYJcREYLYkrb3xbnYmuw-QzOohkgkhrRETcTPJsflg1-jmbe5y3o4h2F9esCHPDM4GnxVPBvAJn9_vF8Xn63efrt6Xtx9vPlxd3pZGKLWUEnkrOWtRWaYG1deSid6iYBxBiRYaicBBKaZUR7FuOjSNQGmGTlrbmr6-KN6ecvdrP6HN3UsEr_fRTRC_6wBO_z2Z3ai34aAlZbUUMge8ug-I4duKadGTy0_wHmYMa9Kc1h1vRS3aLH1zkpoMLkUcHmoY1Ue4eqf_gauPcDUVOsPN_hd_3vXB_ZtmFtycBJh_7OAw6mTc8Teti2gWbYP7z6qftpPGOA</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>O'Keeffe, Linda M.</creator><creator>Howe, Laura D.</creator><creator>Fraser, Abigail</creator><creator>Hughes, Alun D.</creator><creator>Wade, Kaitlin H.</creator><creator>Anderson, Emma L.</creator><creator>Lawlor, Debbie A.</creator><creator>Erzurumluoglu, A. 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Mesut</creatorcontrib><creatorcontrib>Davey-Smith, George</creatorcontrib><creatorcontrib>Rodriguez, Santiago</creatorcontrib><creatorcontrib>Stergiakouli, Evie</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Keeffe, Linda M.</au><au>Howe, Laura D.</au><au>Fraser, Abigail</au><au>Hughes, Alun D.</au><au>Wade, Kaitlin H.</au><au>Anderson, Emma L.</au><au>Lawlor, Debbie A.</au><au>Erzurumluoglu, A. Mesut</au><au>Davey-Smith, George</au><au>Rodriguez, Santiago</au><au>Stergiakouli, Evie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>2018-07</date><risdate>2018</risdate><volume>274</volume><spage>94</spage><epage>103</epage><pages>94-103</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>Males have greater cardiometabolic risk than females, though the reasons for this are poorly understood. The aim of this study was to examine the association between common Y chromosomal haplogroups and cardiometabolic risk during early life.
In a British birth cohort, we examined the association of Y chromosomal haplogroups with trajectories of cardiometabolic risk factors from birth to 18 years and with carotid-femoral pulse wave velocity, carotid intima media thickness and left ventricular mass index at age 18. Haplogroups were grouped according to their phylogenetic relatedness into categories of R, I, E, J, G and all other haplogroups combined (T, Q, H, L, C, N and O). Risk factors included BMI, fat and lean mass, systolic blood pressure (SBP), diastolic blood pressure, pulse rate, triglycerides, high density lipoprotein cholesterol (HDL-c), non-HDL-c and c-reactive protein. Analyses were performed using multilevel models and linear regression, as appropriate.
Y chromosomal haplogroups were not associated with any cardiometabolic risk factors from birth to 18 years. For example, at age 18, the difference in SBP comparing each haplogroup with haplogroup R was −0.39 mmHg (95% Confidence Interval (CI): −0.75, 1.54) for haplogroup I, 2.56 mmHg (95% CI: −0.76, 5.89) for haplogroup E, −0.02 mmHg (95% CI: −2.87, 2.83) for haplogroup J, 1.28 mmHg (95% CI: −4.70, 2.13) for haplogroup G and −2.75 mmHg (95% CI: −6.38, 0.88) for all other haplogroups combined.
Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors during childhood and adolescence or with subclinical cardiovascular measures at age 18.
•Common Y chromosomal haplogroups are not associated with cardiometabolic risk factors from birth to age 18.•Common Y chromosomal haplogroups are not associated with cardiovascular structure and function at age 18.•Common Y chromosomal haplogroups are not associated with cardiometabolic risk in males during early life.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>29753233</pmid><doi>10.1016/j.atherosclerosis.2018.04.027</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0003-0774</orcidid><orcidid>https://orcid.org/0000-0002-7741-9470</orcidid><orcidid>https://orcid.org/0000-0003-1322-8138</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescence Adolescent Age Factors Asymptomatic Diseases Cardiometabolic Cardiovascular Diseases - diagnosis Cardiovascular Diseases - epidemiology Cardiovascular Diseases - genetics Child Child, Preschool Childhood Chromosomes, Human, Y - genetics England - epidemiology Genetic Predisposition to Disease Haplotypes Health Status Humans Infant Infant, Newborn Longitudinal Studies Male Metabolic Syndrome - diagnosis Metabolic Syndrome - epidemiology Metabolic Syndrome - genetics Phenotype Prognosis Prospective Studies Risk Assessment Risk Factors Sex Factors Time Factors Vascular Y chromosome |
title | Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence |
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