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Telomere Shortening in Three Diabetes Mellitus Types in a Mexican Sample
This study aimed to explore the role of telomere length in three different diabetes types: latent autoimmune diabetes of adulthood (LADA), latent autoimmune diabetes in the young (LADY), and type 2 diabetes mellitus (T2DM). A total of 115 patients were included, 72 (62.61%) had LADA, 30 (26.09%) had...
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Published in: | Biomedicines 2023-02, Vol.11 (3), p.730 |
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description | This study aimed to explore the role of telomere length in three different diabetes types: latent autoimmune diabetes of adulthood (LADA), latent autoimmune diabetes in the young (LADY), and type 2 diabetes mellitus (T2DM). A total of 115 patients were included, 72 (62.61%) had LADA, 30 (26.09%) had T2DM, and 13 (11.30%) had LADY. Telomere length was measured using real-time Polymerase Chain Reaction. For statistical analysis, we used the ANOVA test, X2 test, and the Mann-Whitney U test. Patients with T2DM had higher BMI compared to LADA and LADY groups, with a BMI average of 31.32 kg/m
(
= 0.0235). While the LADA group had more patients with comorbidities, there was not a statistically significant difference (
= 0.3164,
= 0.3315,
= 0.3742 for each of the previously mentioned conditions). There was a difference between those patients with T2DM who took metformin plus any other oral antidiabetic agent and those who took metformin plus insulin, the ones who had longer telomeres. LADA patients had shorter telomeres compared to T2DM patients but not LADY patients. Furthermore, T2DM may have longer telomeres thanks to the protective effects of both metformin and insulin, despite the higher BMI in this group. |
doi_str_mv | 10.3390/biomedicines11030730 |
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(
= 0.0235). While the LADA group had more patients with comorbidities, there was not a statistically significant difference (
= 0.3164,
= 0.3315,
= 0.3742 for each of the previously mentioned conditions). There was a difference between those patients with T2DM who took metformin plus any other oral antidiabetic agent and those who took metformin plus insulin, the ones who had longer telomeres. LADA patients had shorter telomeres compared to T2DM patients but not LADY patients. Furthermore, T2DM may have longer telomeres thanks to the protective effects of both metformin and insulin, despite the higher BMI in this group.</description><identifier>ISSN: 2227-9059</identifier><identifier>EISSN: 2227-9059</identifier><identifier>DOI: 10.3390/biomedicines11030730</identifier><identifier>PMID: 36979709</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Autoimmune diseases ; Chromosomes ; Comorbidity ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Disease ; DNA damage ; Health aspects ; Hospitals ; Hyperglycemia ; Insulin ; Insulin resistance ; Laboratories ; Metabolism ; Metformin ; Mexicans ; Oxidative stress ; Patients ; Statistical analysis ; Telomerase ; telomere length ; telomere shortening ; Telomeres</subject><ispartof>Biomedicines, 2023-02, Vol.11 (3), p.730</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-6b8c6aa2cbad2d3037009146d20215eafdd0f49481307e970f8c7bdc667ead8f3</citedby><cites>FETCH-LOGICAL-c570t-6b8c6aa2cbad2d3037009146d20215eafdd0f49481307e970f8c7bdc667ead8f3</cites><orcidid>0000-0001-5536-3173 ; 0000-0001-7717-4541 ; 0000-0003-2494-0067 ; 0000-0001-8170-8171</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2791583907/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2791583907?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36979709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cuevas Diaz, Pavel</creatorcontrib><creatorcontrib>Nicolini, Humberto</creatorcontrib><creatorcontrib>Nolasco-Rosales, German Alberto</creatorcontrib><creatorcontrib>Juarez Rojop, Isela</creatorcontrib><creatorcontrib>Tovilla-Zarate, Carlos Alfonso</creatorcontrib><creatorcontrib>Rodriguez Sanchez, Ester</creatorcontrib><creatorcontrib>Genis-Mendoza, Alma Delia</creatorcontrib><title>Telomere Shortening in Three Diabetes Mellitus Types in a Mexican Sample</title><title>Biomedicines</title><addtitle>Biomedicines</addtitle><description>This study aimed to explore the role of telomere length in three different diabetes types: latent autoimmune diabetes of adulthood (LADA), latent autoimmune diabetes in the young (LADY), and type 2 diabetes mellitus (T2DM). A total of 115 patients were included, 72 (62.61%) had LADA, 30 (26.09%) had T2DM, and 13 (11.30%) had LADY. Telomere length was measured using real-time Polymerase Chain Reaction. For statistical analysis, we used the ANOVA test, X2 test, and the Mann-Whitney U test. Patients with T2DM had higher BMI compared to LADA and LADY groups, with a BMI average of 31.32 kg/m
(
= 0.0235). While the LADA group had more patients with comorbidities, there was not a statistically significant difference (
= 0.3164,
= 0.3315,
= 0.3742 for each of the previously mentioned conditions). There was a difference between those patients with T2DM who took metformin plus any other oral antidiabetic agent and those who took metformin plus insulin, the ones who had longer telomeres. LADA patients had shorter telomeres compared to T2DM patients but not LADY patients. Furthermore, T2DM may have longer telomeres thanks to the protective effects of both metformin and insulin, despite the higher BMI in this group.</description><subject>Autoimmune diseases</subject><subject>Chromosomes</subject><subject>Comorbidity</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Disease</subject><subject>DNA damage</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Hyperglycemia</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Laboratories</subject><subject>Metabolism</subject><subject>Metformin</subject><subject>Mexicans</subject><subject>Oxidative stress</subject><subject>Patients</subject><subject>Statistical analysis</subject><subject>Telomerase</subject><subject>telomere length</subject><subject>telomere shortening</subject><subject>Telomeres</subject><issn>2227-9059</issn><issn>2227-9059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIVqX_AKFIXLhs8Vfs-ISqAm2lIg5dztbEnux6lbUXO0H03-N0S-mi2gfb4_feeJ6nqt5Scsa5Jh87H7fovPUBM6WEE8XJi-qYMaYWmjT65ZP9UXWa84aUoSlvqXhdHXGplVZEH1dXSxyKVML6dh3TiMGHVe1DvVwnxPqzhw5HzPU3HAY_Trle3u3KsQCgxH57C6G-he1uwDfVqx6GjKcP60n14-uX5cXV4ub75fXF-c3CNoqMC9m1VgIw24FjjhOu5mcJ6RhhtEHonSO90KKlpSYsb-xbqzpnpVQIru35SXW913URNmaX_BbSnYngzX0gppWBNHo7oOmZtg1vO9JIFNiTlgJ0EplFoYEoWbQ-7bV2U1fstBjGBMOB6OFN8Guzir8MJUQ0StGi8OFBIcWfE-bRbH22xSwIGKdsmNJMaN1qUaDv_4Nu4pRC8WpG0aYt_6r-oVZQKvChjyWxnUXNuRJcSE7JnPbsGVSZDrfexoC9L_EDgtgTbIo5J-wfi6TEzB1lnuuoQnv31KBH0t_-4X8Aw27IPw</recordid><startdate>20230228</startdate><enddate>20230228</enddate><creator>Cuevas Diaz, Pavel</creator><creator>Nicolini, Humberto</creator><creator>Nolasco-Rosales, German Alberto</creator><creator>Juarez Rojop, Isela</creator><creator>Tovilla-Zarate, Carlos Alfonso</creator><creator>Rodriguez Sanchez, Ester</creator><creator>Genis-Mendoza, Alma Delia</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</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><orcidid>https://orcid.org/0000-0001-5536-3173</orcidid><orcidid>https://orcid.org/0000-0001-7717-4541</orcidid><orcidid>https://orcid.org/0000-0003-2494-0067</orcidid><orcidid>https://orcid.org/0000-0001-8170-8171</orcidid></search><sort><creationdate>20230228</creationdate><title>Telomere Shortening in Three Diabetes Mellitus Types in a Mexican Sample</title><author>Cuevas Diaz, Pavel ; Nicolini, Humberto ; Nolasco-Rosales, German Alberto ; Juarez Rojop, Isela ; Tovilla-Zarate, Carlos Alfonso ; Rodriguez Sanchez, Ester ; Genis-Mendoza, Alma Delia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-6b8c6aa2cbad2d3037009146d20215eafdd0f49481307e970f8c7bdc667ead8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Autoimmune diseases</topic><topic>Chromosomes</topic><topic>Comorbidity</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Disease</topic><topic>DNA damage</topic><topic>Health aspects</topic><topic>Hospitals</topic><topic>Hyperglycemia</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Laboratories</topic><topic>Metabolism</topic><topic>Metformin</topic><topic>Mexicans</topic><topic>Oxidative stress</topic><topic>Patients</topic><topic>Statistical analysis</topic><topic>Telomerase</topic><topic>telomere length</topic><topic>telomere shortening</topic><topic>Telomeres</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cuevas Diaz, Pavel</creatorcontrib><creatorcontrib>Nicolini, Humberto</creatorcontrib><creatorcontrib>Nolasco-Rosales, German Alberto</creatorcontrib><creatorcontrib>Juarez Rojop, Isela</creatorcontrib><creatorcontrib>Tovilla-Zarate, Carlos Alfonso</creatorcontrib><creatorcontrib>Rodriguez Sanchez, Ester</creatorcontrib><creatorcontrib>Genis-Mendoza, Alma Delia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</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>DOAJ: Directory of Open Access Journals</collection><jtitle>Biomedicines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cuevas Diaz, Pavel</au><au>Nicolini, Humberto</au><au>Nolasco-Rosales, German Alberto</au><au>Juarez Rojop, Isela</au><au>Tovilla-Zarate, Carlos Alfonso</au><au>Rodriguez Sanchez, Ester</au><au>Genis-Mendoza, Alma Delia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Telomere Shortening in Three Diabetes Mellitus Types in a Mexican Sample</atitle><jtitle>Biomedicines</jtitle><addtitle>Biomedicines</addtitle><date>2023-02-28</date><risdate>2023</risdate><volume>11</volume><issue>3</issue><spage>730</spage><pages>730-</pages><issn>2227-9059</issn><eissn>2227-9059</eissn><abstract>This study aimed to explore the role of telomere length in three different diabetes types: latent autoimmune diabetes of adulthood (LADA), latent autoimmune diabetes in the young (LADY), and type 2 diabetes mellitus (T2DM). A total of 115 patients were included, 72 (62.61%) had LADA, 30 (26.09%) had T2DM, and 13 (11.30%) had LADY. Telomere length was measured using real-time Polymerase Chain Reaction. For statistical analysis, we used the ANOVA test, X2 test, and the Mann-Whitney U test. Patients with T2DM had higher BMI compared to LADA and LADY groups, with a BMI average of 31.32 kg/m
(
= 0.0235). While the LADA group had more patients with comorbidities, there was not a statistically significant difference (
= 0.3164,
= 0.3315,
= 0.3742 for each of the previously mentioned conditions). There was a difference between those patients with T2DM who took metformin plus any other oral antidiabetic agent and those who took metformin plus insulin, the ones who had longer telomeres. LADA patients had shorter telomeres compared to T2DM patients but not LADY patients. Furthermore, T2DM may have longer telomeres thanks to the protective effects of both metformin and insulin, despite the higher BMI in this group.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36979709</pmid><doi>10.3390/biomedicines11030730</doi><orcidid>https://orcid.org/0000-0001-5536-3173</orcidid><orcidid>https://orcid.org/0000-0001-7717-4541</orcidid><orcidid>https://orcid.org/0000-0003-2494-0067</orcidid><orcidid>https://orcid.org/0000-0001-8170-8171</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Autoimmune diseases Chromosomes Comorbidity Diabetes Diabetes mellitus (non-insulin dependent) Disease DNA damage Health aspects Hospitals Hyperglycemia Insulin Insulin resistance Laboratories Metabolism Metformin Mexicans Oxidative stress Patients Statistical analysis Telomerase telomere length telomere shortening Telomeres |
title | Telomere Shortening in Three Diabetes Mellitus Types in a Mexican Sample |
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