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Age-related changes of human serum Sirtuin6 in adults
Aging is a natural life process and with an aging population, age-related diseases (e.g. type 2 diabetes mellitus (T2DM), atherosclerosis-based cardiovascular diseases) are the primary mortality cause in older adults. Telomerase is often used as an aging biomarker. Detection and characterization of...
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Published in: | BMC geriatrics 2021-08, Vol.21 (1), p.452-452, Article 452 |
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description | Aging is a natural life process and with an aging population, age-related diseases (e.g. type 2 diabetes mellitus (T2DM), atherosclerosis-based cardiovascular diseases) are the primary mortality cause in older adults. Telomerase is often used as an aging biomarker. Detection and characterization of novel biomarkers can help in a more specific and sensitive identification of a person's aging status. Also, this could help in age-related diseases early prevent, ultimately prolonging the population's life span. Sirtuin 6 (Sirt6) - a member of the Sirtuins NAD
-dependent histone deacetylases family - is mainly intracellularly expressed, and is reported to be involved in the regulation of aging and aging-related diseases. Whether serum Sirt6 is correlated with aging and could be used as an aging biomarker is unknown. In the present study, we aimed to investigate the age-related Sirt6 changes in the serum of human adults.
Participants were divided into three groups according to age: 20-30 years (Young); 45-55 years (Middle-aged); and ≥ 70 years (Old). The Sirt6 and telomerase serum concentrations were determined by ELISA. The Sirt6 and human telomerase reverse transcriptase (hTERT) expression in vessels from amputated human lower limbs were analyzed using real-time quantitative PCR (RT-qPCR) and immunohistochemical staining. The relationships between variables were evaluated by Pearson correlation analysis.
The Sirt6 and telomerase serum levels reduced with an increase in age. A similar tendency was observed for Sirt6 and hTERT in the vessel. Serum levels of Sirt6 were higher in females compared with males. Pearson's regression analysis revealed that the Sirt6 serum level positively correlated with telomerase (r = 0.5743) and both were significantly negatively correlated with age (r = - 0.5830 and r = - 0.5993, respectively).
We reported a negative correlation between serum Sirt6 concentration and aging in human beings. Therefore, the Sirt6 serum level is a potential sex-specific aging marker. |
doi_str_mv | 10.1186/s12877-021-02399-0 |
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-dependent histone deacetylases family - is mainly intracellularly expressed, and is reported to be involved in the regulation of aging and aging-related diseases. Whether serum Sirt6 is correlated with aging and could be used as an aging biomarker is unknown. In the present study, we aimed to investigate the age-related Sirt6 changes in the serum of human adults.
Participants were divided into three groups according to age: 20-30 years (Young); 45-55 years (Middle-aged); and ≥ 70 years (Old). The Sirt6 and telomerase serum concentrations were determined by ELISA. The Sirt6 and human telomerase reverse transcriptase (hTERT) expression in vessels from amputated human lower limbs were analyzed using real-time quantitative PCR (RT-qPCR) and immunohistochemical staining. The relationships between variables were evaluated by Pearson correlation analysis.
The Sirt6 and telomerase serum levels reduced with an increase in age. A similar tendency was observed for Sirt6 and hTERT in the vessel. Serum levels of Sirt6 were higher in females compared with males. Pearson's regression analysis revealed that the Sirt6 serum level positively correlated with telomerase (r = 0.5743) and both were significantly negatively correlated with age (r = - 0.5830 and r = - 0.5993, respectively).
We reported a negative correlation between serum Sirt6 concentration and aging in human beings. Therefore, the Sirt6 serum level is a potential sex-specific aging marker.</description><identifier>ISSN: 1471-2318</identifier><identifier>EISSN: 1471-2318</identifier><identifier>DOI: 10.1186/s12877-021-02399-0</identifier><identifier>PMID: 34348649</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Age groups ; Aged ; Aging ; Arteriosclerosis ; Biological markers ; Biomarker ; Biomarkers ; Cardiovascular diseases ; Correlation analysis ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 ; Enzyme-linked immunosorbent assay ; Female ; Geriatrics ; Health aspects ; Histones ; Hospitals ; Humans ; Life cycle, Human ; Life span ; Male ; Males ; Middle age ; Middle Aged ; NAD ; Older people ; Physiological aspects ; Physiology ; RNA-directed DNA polymerase ; Serum levels ; Sirt6 ; Sirtuins ; Sirtuins - blood ; Statistical analysis ; Telomerase ; Telomerase reverse transcriptase ; Transferases ; Young Adult</subject><ispartof>BMC geriatrics, 2021-08, Vol.21 (1), p.452-452, Article 452</ispartof><rights>2021. The Author(s).</rights><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-a1acabf5d7ee99eaca4b5b5513f7be575d213235d7480077c55be8e4e8f36ba13</citedby><cites>FETCH-LOGICAL-c563t-a1acabf5d7ee99eaca4b5b5513f7be575d213235d7480077c55be8e4e8f36ba13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8335874/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2562510181?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34348649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Ying</creatorcontrib><creatorcontrib>Bai, Xiangli</creatorcontrib><creatorcontrib>Jia, Xiong</creatorcontrib><creatorcontrib>Lu, Yajing</creatorcontrib><creatorcontrib>Cheng, Wenzhuo</creatorcontrib><creatorcontrib>Shu, Meng</creatorcontrib><creatorcontrib>Zhu, Yan</creatorcontrib><creatorcontrib>Zhu, Lin</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Shu, Yan</creatorcontrib><creatorcontrib>Song, Yi</creatorcontrib><creatorcontrib>Jin, Si</creatorcontrib><title>Age-related changes of human serum Sirtuin6 in adults</title><title>BMC geriatrics</title><addtitle>BMC Geriatr</addtitle><description>Aging is a natural life process and with an aging population, age-related diseases (e.g. type 2 diabetes mellitus (T2DM), atherosclerosis-based cardiovascular diseases) are the primary mortality cause in older adults. Telomerase is often used as an aging biomarker. Detection and characterization of novel biomarkers can help in a more specific and sensitive identification of a person's aging status. Also, this could help in age-related diseases early prevent, ultimately prolonging the population's life span. Sirtuin 6 (Sirt6) - a member of the Sirtuins NAD
-dependent histone deacetylases family - is mainly intracellularly expressed, and is reported to be involved in the regulation of aging and aging-related diseases. Whether serum Sirt6 is correlated with aging and could be used as an aging biomarker is unknown. In the present study, we aimed to investigate the age-related Sirt6 changes in the serum of human adults.
Participants were divided into three groups according to age: 20-30 years (Young); 45-55 years (Middle-aged); and ≥ 70 years (Old). The Sirt6 and telomerase serum concentrations were determined by ELISA. The Sirt6 and human telomerase reverse transcriptase (hTERT) expression in vessels from amputated human lower limbs were analyzed using real-time quantitative PCR (RT-qPCR) and immunohistochemical staining. The relationships between variables were evaluated by Pearson correlation analysis.
The Sirt6 and telomerase serum levels reduced with an increase in age. A similar tendency was observed for Sirt6 and hTERT in the vessel. Serum levels of Sirt6 were higher in females compared with males. Pearson's regression analysis revealed that the Sirt6 serum level positively correlated with telomerase (r = 0.5743) and both were significantly negatively correlated with age (r = - 0.5830 and r = - 0.5993, respectively).
We reported a negative correlation between serum Sirt6 concentration and aging in human beings. Therefore, the Sirt6 serum level is a potential sex-specific aging marker.</description><subject>Adult</subject><subject>Age groups</subject><subject>Aged</subject><subject>Aging</subject><subject>Arteriosclerosis</subject><subject>Biological markers</subject><subject>Biomarker</subject><subject>Biomarkers</subject><subject>Cardiovascular diseases</subject><subject>Correlation analysis</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Female</subject><subject>Geriatrics</subject><subject>Health aspects</subject><subject>Histones</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Life cycle, Human</subject><subject>Life span</subject><subject>Male</subject><subject>Males</subject><subject>Middle age</subject><subject>Middle Aged</subject><subject>NAD</subject><subject>Older people</subject><subject>Physiological aspects</subject><subject>Physiology</subject><subject>RNA-directed DNA polymerase</subject><subject>Serum levels</subject><subject>Sirt6</subject><subject>Sirtuins</subject><subject>Sirtuins - blood</subject><subject>Statistical analysis</subject><subject>Telomerase</subject><subject>Telomerase reverse transcriptase</subject><subject>Transferases</subject><subject>Young Adult</subject><issn>1471-2318</issn><issn>1471-2318</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1rFTEQhhdRbK3-AS9kwRtvtuZzk70RDsXWQsEL9TrkY7Inh92kJrsF_705PbX2iISQZOadJ8zwNs1bjM4xlv3HgokUokME102HoUPPmlPMBO4IxfL5k_tJ86qUHUJYSNK_bE4oo0z2bDht-GaELsOkF3Ct3eo4QmmTb7frrGNbIK9z-y3kZQ2xb0NstVunpbxuXng9FXjzcJ41Py4_f7_40t18vbq-2Nx0lvd06TTWVhvPnQAYBqgPZrjhHFMvDHDBHcGU0JpnEiEhLOcGJDCQnvZGY3rWXB-4Lumdus1h1vmXSjqo-0DKo9J5CXYCJankTns_mNoYIkbagSLWM6YdA0J8ZX06sG5XM4OzEJespyPocSaGrRrTXSVTLgWrgA8PgJx-rlAWNYdiYZp0hLQWRTiXrDZFeZW-_0e6S2uOdVRV1ROOEZb4r2rUtYEQfar_2j1UbXpBiESD2LPO_6Oqy8EcbIrgQ40fFZBDgc2plAz-sUeM1N446mAcVY2j7o2jUC1693Q6jyV_nEJ_A9-su8E</recordid><startdate>20210804</startdate><enddate>20210804</enddate><creator>Zhao, Ying</creator><creator>Bai, Xiangli</creator><creator>Jia, Xiong</creator><creator>Lu, Yajing</creator><creator>Cheng, Wenzhuo</creator><creator>Shu, Meng</creator><creator>Zhu, Yan</creator><creator>Zhu, Lin</creator><creator>Wang, Li</creator><creator>Shu, Yan</creator><creator>Song, Yi</creator><creator>Jin, Si</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20210804</creationdate><title>Age-related changes of human serum Sirtuin6 in adults</title><author>Zhao, Ying ; Bai, Xiangli ; Jia, Xiong ; Lu, Yajing ; Cheng, Wenzhuo ; Shu, Meng ; Zhu, Yan ; Zhu, Lin ; Wang, Li ; Shu, Yan ; Song, Yi ; Jin, Si</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-a1acabf5d7ee99eaca4b5b5513f7be575d213235d7480077c55be8e4e8f36ba13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Age groups</topic><topic>Aged</topic><topic>Aging</topic><topic>Arteriosclerosis</topic><topic>Biological markers</topic><topic>Biomarker</topic><topic>Biomarkers</topic><topic>Cardiovascular diseases</topic><topic>Correlation analysis</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Female</topic><topic>Geriatrics</topic><topic>Health aspects</topic><topic>Histones</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Life cycle, Human</topic><topic>Life span</topic><topic>Male</topic><topic>Males</topic><topic>Middle age</topic><topic>Middle Aged</topic><topic>NAD</topic><topic>Older people</topic><topic>Physiological aspects</topic><topic>Physiology</topic><topic>RNA-directed DNA polymerase</topic><topic>Serum levels</topic><topic>Sirt6</topic><topic>Sirtuins</topic><topic>Sirtuins - blood</topic><topic>Statistical analysis</topic><topic>Telomerase</topic><topic>Telomerase reverse transcriptase</topic><topic>Transferases</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Ying</creatorcontrib><creatorcontrib>Bai, Xiangli</creatorcontrib><creatorcontrib>Jia, Xiong</creatorcontrib><creatorcontrib>Lu, Yajing</creatorcontrib><creatorcontrib>Cheng, Wenzhuo</creatorcontrib><creatorcontrib>Shu, Meng</creatorcontrib><creatorcontrib>Zhu, Yan</creatorcontrib><creatorcontrib>Zhu, Lin</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Shu, Yan</creatorcontrib><creatorcontrib>Song, Yi</creatorcontrib><creatorcontrib>Jin, Si</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals(OpenAccess)</collection><jtitle>BMC geriatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Ying</au><au>Bai, Xiangli</au><au>Jia, Xiong</au><au>Lu, Yajing</au><au>Cheng, Wenzhuo</au><au>Shu, Meng</au><au>Zhu, Yan</au><au>Zhu, Lin</au><au>Wang, Li</au><au>Shu, Yan</au><au>Song, Yi</au><au>Jin, Si</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Age-related changes of human serum Sirtuin6 in adults</atitle><jtitle>BMC geriatrics</jtitle><addtitle>BMC Geriatr</addtitle><date>2021-08-04</date><risdate>2021</risdate><volume>21</volume><issue>1</issue><spage>452</spage><epage>452</epage><pages>452-452</pages><artnum>452</artnum><issn>1471-2318</issn><eissn>1471-2318</eissn><abstract>Aging is a natural life process and with an aging population, age-related diseases (e.g. type 2 diabetes mellitus (T2DM), atherosclerosis-based cardiovascular diseases) are the primary mortality cause in older adults. Telomerase is often used as an aging biomarker. Detection and characterization of novel biomarkers can help in a more specific and sensitive identification of a person's aging status. Also, this could help in age-related diseases early prevent, ultimately prolonging the population's life span. Sirtuin 6 (Sirt6) - a member of the Sirtuins NAD
-dependent histone deacetylases family - is mainly intracellularly expressed, and is reported to be involved in the regulation of aging and aging-related diseases. Whether serum Sirt6 is correlated with aging and could be used as an aging biomarker is unknown. In the present study, we aimed to investigate the age-related Sirt6 changes in the serum of human adults.
Participants were divided into three groups according to age: 20-30 years (Young); 45-55 years (Middle-aged); and ≥ 70 years (Old). The Sirt6 and telomerase serum concentrations were determined by ELISA. The Sirt6 and human telomerase reverse transcriptase (hTERT) expression in vessels from amputated human lower limbs were analyzed using real-time quantitative PCR (RT-qPCR) and immunohistochemical staining. The relationships between variables were evaluated by Pearson correlation analysis.
The Sirt6 and telomerase serum levels reduced with an increase in age. A similar tendency was observed for Sirt6 and hTERT in the vessel. Serum levels of Sirt6 were higher in females compared with males. Pearson's regression analysis revealed that the Sirt6 serum level positively correlated with telomerase (r = 0.5743) and both were significantly negatively correlated with age (r = - 0.5830 and r = - 0.5993, respectively).
We reported a negative correlation between serum Sirt6 concentration and aging in human beings. Therefore, the Sirt6 serum level is a potential sex-specific aging marker.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>34348649</pmid><doi>10.1186/s12877-021-02399-0</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Age groups Aged Aging Arteriosclerosis Biological markers Biomarker Biomarkers Cardiovascular diseases Correlation analysis Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 Enzyme-linked immunosorbent assay Female Geriatrics Health aspects Histones Hospitals Humans Life cycle, Human Life span Male Males Middle age Middle Aged NAD Older people Physiological aspects Physiology RNA-directed DNA polymerase Serum levels Sirt6 Sirtuins Sirtuins - blood Statistical analysis Telomerase Telomerase reverse transcriptase Transferases Young Adult |
title | Age-related changes of human serum Sirtuin6 in adults |
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