Association of puberty timing with type 2 diabetes: A systematic review and meta-analysis
Emerging studies have investigated the association between puberty timing, particularly age at menarche (AAM), and type 2 diabetes. However, whether this association is independent of adiposity is unclear. We aimed to systematically review published evidence on the association between puberty timing...
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description | Emerging studies have investigated the association between puberty timing, particularly age at menarche (AAM), and type 2 diabetes. However, whether this association is independent of adiposity is unclear. We aimed to systematically review published evidence on the association between puberty timing and type 2 diabetes (T2D) or impaired glucose tolerance (IGT), with and without adjustment for adiposity, and to estimate the potential contribution of puberty timing to the burden of T2D in the United Kingdom (UK).
We searched PubMed, Medline, and Embase databases for publications until February 2019 on the timing of any secondary sexual characteristic in boys or girls in relation to T2D/IGT. Inverse-variance-weighted random-effects meta-analysis was used to pool reported estimates, and meta-regression was used to explore sources of heterogeneity. Twenty-eight observational studies were identified. All assessed AAM in women (combined N = 1,228,306); only 1 study additionally included men. In models without adjustment for adult adiposity, T2D/IGT risk was lower per year later AAM (relative risk [RR] = 0.91, 95% CI 0.89-0.93, p < 0.001, 11 estimates, n = 833,529, I2 = 85.4%) and higher for early versus later menarche (RR = 1.39, 95% CI 1.25-1.55, p < 0.001, 23 estimates, n = 1,185,444, I2 = 87.8%). Associations were weaker but still evident in models adjusted for adiposity (AAM: RR = 0.97 per year, 95% CI 0.95-0.98, p < 0.001, 12 estimates, n = 852,268, I2 = 51.8%; early menarche: RR = 1.19, 95% CI 1.11-1.28, p < 0.001, 21 estimates, n = 890,583, I2 = 68.1%). Associations were stronger among white than Asian women, and in populations with earlier average AAM. The estimated population attributable risk of T2D in white UK women due to early menarche unadjusted and adjusted for adiposity was 12.6% (95% CI 11.0-14.3) and 5.1% (95% CI 3.6-6.7), respectively. Findings in this study are limited by residual and unmeasured confounding, and self-reported AAM.
Earlier AAM is consistently associated with higher T2D/IGT risk, independent of adiposity. More importantly, this research has identified that a substantial proportion of T2D in women is related to early menarche, which would be expected to increase in light of global secular trends towards earlier puberty timing. These findings highlight the need to identify the underlying mechanisms linking early menarche to T2D/IGT risk. |
doi_str_mv | 10.1371/journal.pmed.1003017 |
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We searched PubMed, Medline, and Embase databases for publications until February 2019 on the timing of any secondary sexual characteristic in boys or girls in relation to T2D/IGT. Inverse-variance-weighted random-effects meta-analysis was used to pool reported estimates, and meta-regression was used to explore sources of heterogeneity. Twenty-eight observational studies were identified. All assessed AAM in women (combined N = 1,228,306); only 1 study additionally included men. In models without adjustment for adult adiposity, T2D/IGT risk was lower per year later AAM (relative risk [RR] = 0.91, 95% CI 0.89-0.93, p < 0.001, 11 estimates, n = 833,529, I2 = 85.4%) and higher for early versus later menarche (RR = 1.39, 95% CI 1.25-1.55, p < 0.001, 23 estimates, n = 1,185,444, I2 = 87.8%). Associations were weaker but still evident in models adjusted for adiposity (AAM: RR = 0.97 per year, 95% CI 0.95-0.98, p < 0.001, 12 estimates, n = 852,268, I2 = 51.8%; early menarche: RR = 1.19, 95% CI 1.11-1.28, p < 0.001, 21 estimates, n = 890,583, I2 = 68.1%). Associations were stronger among white than Asian women, and in populations with earlier average AAM. The estimated population attributable risk of T2D in white UK women due to early menarche unadjusted and adjusted for adiposity was 12.6% (95% CI 11.0-14.3) and 5.1% (95% CI 3.6-6.7), respectively. Findings in this study are limited by residual and unmeasured confounding, and self-reported AAM.
Earlier AAM is consistently associated with higher T2D/IGT risk, independent of adiposity. More importantly, this research has identified that a substantial proportion of T2D in women is related to early menarche, which would be expected to increase in light of global secular trends towards earlier puberty timing. These findings highlight the need to identify the underlying mechanisms linking early menarche to T2D/IGT risk.</description><identifier>ISSN: 1549-1676</identifier><identifier>ISSN: 1549-1277</identifier><identifier>EISSN: 1549-1676</identifier><identifier>DOI: 10.1371/journal.pmed.1003017</identifier><identifier>PMID: 31905226</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adipose tissue ; Adiposity - physiology ; Age ; Age Factors ; Biology and Life Sciences ; Body mass index ; Children & youth ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - diagnosis ; Diabetes Mellitus, Type 2 - epidemiology ; Diabetes Mellitus, Type 2 - metabolism ; Epidemiology ; Estimates ; Female ; Glucose ; Glucose tolerance ; Hemoglobin ; Humans ; Longitudinal studies ; Male ; Medicine and Health Sciences ; Menarche ; Menarche - metabolism ; Meta-analysis ; Metabolism ; Observational Studies as Topic - methods ; People and Places ; Physical Sciences ; Population ; Puberty ; Puberty - metabolism ; Research and Analysis Methods ; Systematic review ; Trends ; Womens health</subject><ispartof>PLoS medicine, 2020-01, Vol.17 (1), p.e1003017-e1003017</ispartof><rights>2020 Cheng et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Cheng et al 2020 Cheng et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-1564ac106c0770313290c7d4ea566f51474da8db5621c2f234f257ff7e47f3883</citedby><cites>FETCH-LOGICAL-c526t-1564ac106c0770313290c7d4ea566f51474da8db5621c2f234f257ff7e47f3883</cites><orcidid>0000-0003-4442-7332 ; 0000-0003-3789-7651 ; 0000-0003-4689-7530</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944335/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944335/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53770,53772,79347,79348</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31905226$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ma, Ronald Ching Wan</contributor><creatorcontrib>Cheng, Tuck Seng</creatorcontrib><creatorcontrib>Day, Felix R</creatorcontrib><creatorcontrib>Lakshman, Rajalakshmi</creatorcontrib><creatorcontrib>Ong, Ken K</creatorcontrib><title>Association of puberty timing with type 2 diabetes: A systematic review and meta-analysis</title><title>PLoS medicine</title><addtitle>PLoS Med</addtitle><description>Emerging studies have investigated the association between puberty timing, particularly age at menarche (AAM), and type 2 diabetes. However, whether this association is independent of adiposity is unclear. We aimed to systematically review published evidence on the association between puberty timing and type 2 diabetes (T2D) or impaired glucose tolerance (IGT), with and without adjustment for adiposity, and to estimate the potential contribution of puberty timing to the burden of T2D in the United Kingdom (UK).
We searched PubMed, Medline, and Embase databases for publications until February 2019 on the timing of any secondary sexual characteristic in boys or girls in relation to T2D/IGT. Inverse-variance-weighted random-effects meta-analysis was used to pool reported estimates, and meta-regression was used to explore sources of heterogeneity. Twenty-eight observational studies were identified. All assessed AAM in women (combined N = 1,228,306); only 1 study additionally included men. In models without adjustment for adult adiposity, T2D/IGT risk was lower per year later AAM (relative risk [RR] = 0.91, 95% CI 0.89-0.93, p < 0.001, 11 estimates, n = 833,529, I2 = 85.4%) and higher for early versus later menarche (RR = 1.39, 95% CI 1.25-1.55, p < 0.001, 23 estimates, n = 1,185,444, I2 = 87.8%). Associations were weaker but still evident in models adjusted for adiposity (AAM: RR = 0.97 per year, 95% CI 0.95-0.98, p < 0.001, 12 estimates, n = 852,268, I2 = 51.8%; early menarche: RR = 1.19, 95% CI 1.11-1.28, p < 0.001, 21 estimates, n = 890,583, I2 = 68.1%). Associations were stronger among white than Asian women, and in populations with earlier average AAM. The estimated population attributable risk of T2D in white UK women due to early menarche unadjusted and adjusted for adiposity was 12.6% (95% CI 11.0-14.3) and 5.1% (95% CI 3.6-6.7), respectively. Findings in this study are limited by residual and unmeasured confounding, and self-reported AAM.
Earlier AAM is consistently associated with higher T2D/IGT risk, independent of adiposity. More importantly, this research has identified that a substantial proportion of T2D in women is related to early menarche, which would be expected to increase in light of global secular trends towards earlier puberty timing. These findings highlight the need to identify the underlying mechanisms linking early menarche to T2D/IGT risk.</description><subject>Adipose tissue</subject><subject>Adiposity - physiology</subject><subject>Age</subject><subject>Age Factors</subject><subject>Biology and Life Sciences</subject><subject>Body mass index</subject><subject>Children & youth</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - diagnosis</subject><subject>Diabetes Mellitus, Type 2 - epidemiology</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Epidemiology</subject><subject>Estimates</subject><subject>Female</subject><subject>Glucose</subject><subject>Glucose tolerance</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Longitudinal studies</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Menarche</subject><subject>Menarche - metabolism</subject><subject>Meta-analysis</subject><subject>Metabolism</subject><subject>Observational Studies as Topic - methods</subject><subject>People and Places</subject><subject>Physical Sciences</subject><subject>Population</subject><subject>Puberty</subject><subject>Puberty - metabolism</subject><subject>Research and Analysis Methods</subject><subject>Systematic review</subject><subject>Trends</subject><subject>Womens health</subject><issn>1549-1676</issn><issn>1549-1277</issn><issn>1549-1676</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>DOA</sourceid><recordid>eNptUktv1DAYjBCIlsI_QGCJC5csfjvhgLSqeFSqxAUOnKwvfmy9SuLF9rbaf4_LplWLONmyZ-ab-TRN85rgFWGKfNjGfZphXO0mZ1cEY4aJetKcEsH7lkglnz64nzQvct5iTHvc4-fNCSM9FpTK0-bXOudoApQQZxQ92u0Hl8oBlTCFeYNuQrlC5bBziCIbYHDF5Y9ojfIhFzdVlkHJXQd3g2C2aHIFWqimDjnkl80zD2N2r5bzrPn55fOP82_t5fevF-fry9YIKktLhORgCJYGK4UZYdWjUZY7EFJ6QbjiFjo7CEmJoZ4y7qlQ3ivHlWddx86at0fd3RizXraSNeUSq070nFbExRFhI2z1LoUJ0kFHCPrvQ0wbDalGGZ0GbP1ghWQUPJeSAidKEWuFERITYFXr0zJtP9TFGzeXBOMj0cc_c7jSm3itZc85Y6IKvF8EUvy9d7noKWTjxhFmF_fVN2Oc8o71vELf_QP9fzp-RJkUc07O35shWN825Y6lb5uil6ZU2puHQe5Jd9VgfwAWKrtu</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Cheng, Tuck Seng</creator><creator>Day, Felix R</creator><creator>Lakshman, Rajalakshmi</creator><creator>Ong, Ken K</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>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><scope>CZK</scope><orcidid>https://orcid.org/0000-0003-4442-7332</orcidid><orcidid>https://orcid.org/0000-0003-3789-7651</orcidid><orcidid>https://orcid.org/0000-0003-4689-7530</orcidid></search><sort><creationdate>20200101</creationdate><title>Association of puberty timing with type 2 diabetes: A systematic review and meta-analysis</title><author>Cheng, Tuck Seng ; Day, Felix R ; Lakshman, Rajalakshmi ; Ong, Ken K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-1564ac106c0770313290c7d4ea566f51474da8db5621c2f234f257ff7e47f3883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adipose tissue</topic><topic>Adiposity - physiology</topic><topic>Age</topic><topic>Age Factors</topic><topic>Biology and Life Sciences</topic><topic>Body mass index</topic><topic>Children & youth</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2 - diagnosis</topic><topic>Diabetes Mellitus, Type 2 - epidemiology</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Epidemiology</topic><topic>Estimates</topic><topic>Female</topic><topic>Glucose</topic><topic>Glucose tolerance</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Longitudinal studies</topic><topic>Male</topic><topic>Medicine and Health Sciences</topic><topic>Menarche</topic><topic>Menarche - metabolism</topic><topic>Meta-analysis</topic><topic>Metabolism</topic><topic>Observational Studies as Topic - methods</topic><topic>People and Places</topic><topic>Physical Sciences</topic><topic>Population</topic><topic>Puberty</topic><topic>Puberty - metabolism</topic><topic>Research and Analysis Methods</topic><topic>Systematic review</topic><topic>Trends</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Tuck Seng</creatorcontrib><creatorcontrib>Day, Felix R</creatorcontrib><creatorcontrib>Lakshman, Rajalakshmi</creatorcontrib><creatorcontrib>Ong, Ken K</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>Neurosciences Abstracts</collection><collection>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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>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>Medical 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><collection>PLoS Medicine</collection><jtitle>PLoS medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, Tuck Seng</au><au>Day, Felix R</au><au>Lakshman, Rajalakshmi</au><au>Ong, Ken K</au><au>Ma, Ronald Ching Wan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of puberty timing with type 2 diabetes: A systematic review and meta-analysis</atitle><jtitle>PLoS medicine</jtitle><addtitle>PLoS Med</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>17</volume><issue>1</issue><spage>e1003017</spage><epage>e1003017</epage><pages>e1003017-e1003017</pages><issn>1549-1676</issn><issn>1549-1277</issn><eissn>1549-1676</eissn><abstract>Emerging studies have investigated the association between puberty timing, particularly age at menarche (AAM), and type 2 diabetes. However, whether this association is independent of adiposity is unclear. We aimed to systematically review published evidence on the association between puberty timing and type 2 diabetes (T2D) or impaired glucose tolerance (IGT), with and without adjustment for adiposity, and to estimate the potential contribution of puberty timing to the burden of T2D in the United Kingdom (UK).
We searched PubMed, Medline, and Embase databases for publications until February 2019 on the timing of any secondary sexual characteristic in boys or girls in relation to T2D/IGT. Inverse-variance-weighted random-effects meta-analysis was used to pool reported estimates, and meta-regression was used to explore sources of heterogeneity. Twenty-eight observational studies were identified. All assessed AAM in women (combined N = 1,228,306); only 1 study additionally included men. In models without adjustment for adult adiposity, T2D/IGT risk was lower per year later AAM (relative risk [RR] = 0.91, 95% CI 0.89-0.93, p < 0.001, 11 estimates, n = 833,529, I2 = 85.4%) and higher for early versus later menarche (RR = 1.39, 95% CI 1.25-1.55, p < 0.001, 23 estimates, n = 1,185,444, I2 = 87.8%). Associations were weaker but still evident in models adjusted for adiposity (AAM: RR = 0.97 per year, 95% CI 0.95-0.98, p < 0.001, 12 estimates, n = 852,268, I2 = 51.8%; early menarche: RR = 1.19, 95% CI 1.11-1.28, p < 0.001, 21 estimates, n = 890,583, I2 = 68.1%). Associations were stronger among white than Asian women, and in populations with earlier average AAM. The estimated population attributable risk of T2D in white UK women due to early menarche unadjusted and adjusted for adiposity was 12.6% (95% CI 11.0-14.3) and 5.1% (95% CI 3.6-6.7), respectively. Findings in this study are limited by residual and unmeasured confounding, and self-reported AAM.
Earlier AAM is consistently associated with higher T2D/IGT risk, independent of adiposity. More importantly, this research has identified that a substantial proportion of T2D in women is related to early menarche, which would be expected to increase in light of global secular trends towards earlier puberty timing. These findings highlight the need to identify the underlying mechanisms linking early menarche to T2D/IGT risk.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31905226</pmid><doi>10.1371/journal.pmed.1003017</doi><orcidid>https://orcid.org/0000-0003-4442-7332</orcidid><orcidid>https://orcid.org/0000-0003-3789-7651</orcidid><orcidid>https://orcid.org/0000-0003-4689-7530</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adipose tissue Adiposity - physiology Age Age Factors Biology and Life Sciences Body mass index Children & youth Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - diagnosis Diabetes Mellitus, Type 2 - epidemiology Diabetes Mellitus, Type 2 - metabolism Epidemiology Estimates Female Glucose Glucose tolerance Hemoglobin Humans Longitudinal studies Male Medicine and Health Sciences Menarche Menarche - metabolism Meta-analysis Metabolism Observational Studies as Topic - methods People and Places Physical Sciences Population Puberty Puberty - metabolism Research and Analysis Methods Systematic review Trends Womens health |
title | Association of puberty timing with type 2 diabetes: A systematic review and meta-analysis |
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