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Family coaggregation of type 1 diabetes mellitus, major depressive disorder, attention-deficiency hyperactivity disorder and autism spectrum disorder in affected families: a nationwide study
Aims This study aimed to examine the risk of T1D, major depressive disorder (MDD), attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), in first-degree relatives (FDRs) of patients with T1D. Methods We enrolled 24,555 FDRs of individuals with T1D and 1:4 matched co...
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Published in: | Acta diabetologica 2023-04, Vol.60 (4), p.517-525 |
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creator | Hsu, Tien-Wei Chen, Mu-Hong Bai, Ya-Mei Chang, Wen-Han Cheng, Chih-Ming Su, Tung-Ping Chen, Tzeng-Ji Tsai, Shih-Jen Liang, Chih-Sung |
description | Aims
This study aimed to examine the risk of T1D, major depressive disorder (MDD), attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), in first-degree relatives (FDRs) of patients with T1D.
Methods
We enrolled 24,555 FDRs of individuals with T1D and 1:4 matched controls (
N
= 98,220) based on age and sex using data from the Taiwan National Health Insurance Research Database between 2001 and 2011. Poisson regression analyses were performed to estimate the risks of MDD, attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder among the FDRs. Finally, we assessed the impact of DKA in the familial coaggregation.
Results
After adjusting for demographic characteristics, FDRs of individuals with T1D had higher risk of T1D (reported as relative risk with 95% confidence interval: 46.07, 33.36–63.63) and MDD (1.17, 1.04–1.32) than controls. Stratified by sex, female FDRs had increased risk of MDD (1.30, 1.13–1.51), while male FDRs had increased risk of ADHD (1.21, 1.01–1.44). Stratified by kinship, parents of individuals with T1D had increased risk of MDD (1.24, 1.06–1.44); offspring of individuals with T1D had increased risk of ADHD (1.41, 1.11–1.79). Importantly, FDRs of individuals with T1D and DKA had higher risk of MDD (1.35, 1.11–1.64) and ADHD (1.40, 1.07–1.82) than controls; however, such risks were not observed in FDRs of individuals with T1D but without DKA.
Conclusions
The individual risks of T1D, MDD, and ADHD were increased in families that included patients with T1D, and DKA might play a role in such coaggregation with MDD and ADHD. Future studies are warranted to investigate the underlying mechanisms. |
doi_str_mv | 10.1007/s00592-022-02025-4 |
format | article |
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This study aimed to examine the risk of T1D, major depressive disorder (MDD), attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), in first-degree relatives (FDRs) of patients with T1D.
Methods
We enrolled 24,555 FDRs of individuals with T1D and 1:4 matched controls (
N
= 98,220) based on age and sex using data from the Taiwan National Health Insurance Research Database between 2001 and 2011. Poisson regression analyses were performed to estimate the risks of MDD, attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder among the FDRs. Finally, we assessed the impact of DKA in the familial coaggregation.
Results
After adjusting for demographic characteristics, FDRs of individuals with T1D had higher risk of T1D (reported as relative risk with 95% confidence interval: 46.07, 33.36–63.63) and MDD (1.17, 1.04–1.32) than controls. Stratified by sex, female FDRs had increased risk of MDD (1.30, 1.13–1.51), while male FDRs had increased risk of ADHD (1.21, 1.01–1.44). Stratified by kinship, parents of individuals with T1D had increased risk of MDD (1.24, 1.06–1.44); offspring of individuals with T1D had increased risk of ADHD (1.41, 1.11–1.79). Importantly, FDRs of individuals with T1D and DKA had higher risk of MDD (1.35, 1.11–1.64) and ADHD (1.40, 1.07–1.82) than controls; however, such risks were not observed in FDRs of individuals with T1D but without DKA.
Conclusions
The individual risks of T1D, MDD, and ADHD were increased in families that included patients with T1D, and DKA might play a role in such coaggregation with MDD and ADHD. Future studies are warranted to investigate the underlying mechanisms.</description><identifier>ISSN: 1432-5233</identifier><identifier>ISSN: 0940-5429</identifier><identifier>EISSN: 1432-5233</identifier><identifier>DOI: 10.1007/s00592-022-02025-4</identifier><identifier>PMID: 36637529</identifier><language>eng</language><publisher>Milan: Springer Milan</publisher><subject>Attention Deficit Disorder with Hyperactivity - epidemiology ; Attention Deficit Disorder with Hyperactivity - genetics ; Attention deficit hyperactivity disorder ; Autism ; Autism Spectrum Disorder - etiology ; Autism Spectrum Disorder - genetics ; Depressive Disorder, Major - complications ; Depressive Disorder, Major - epidemiology ; Depressive Disorder, Major - genetics ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes Mellitus, Type 1 - complications ; Female ; Humans ; Hyperactivity ; Internal Medicine ; Male ; Medicine ; Medicine & Public Health ; Mental depression ; Metabolic Diseases ; Original Article ; Parents</subject><ispartof>Acta diabetologica, 2023-04, Vol.60 (4), p.517-525</ispartof><rights>Springer-Verlag Italia S.r.l., part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. Springer-Verlag Italia S.r.l., part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-1d7751065112566237c814f418ea1aa0f74a4e9a7497982361aab206a94c981c3</citedby><cites>FETCH-LOGICAL-c375t-1d7751065112566237c814f418ea1aa0f74a4e9a7497982361aab206a94c981c3</cites><orcidid>0000-0003-1138-5586 ; 0000-0002-9987-022X</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/36637529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsu, Tien-Wei</creatorcontrib><creatorcontrib>Chen, Mu-Hong</creatorcontrib><creatorcontrib>Bai, Ya-Mei</creatorcontrib><creatorcontrib>Chang, Wen-Han</creatorcontrib><creatorcontrib>Cheng, Chih-Ming</creatorcontrib><creatorcontrib>Su, Tung-Ping</creatorcontrib><creatorcontrib>Chen, Tzeng-Ji</creatorcontrib><creatorcontrib>Tsai, Shih-Jen</creatorcontrib><creatorcontrib>Liang, Chih-Sung</creatorcontrib><title>Family coaggregation of type 1 diabetes mellitus, major depressive disorder, attention-deficiency hyperactivity disorder and autism spectrum disorder in affected families: a nationwide study</title><title>Acta diabetologica</title><addtitle>Acta Diabetol</addtitle><addtitle>Acta Diabetol</addtitle><description>Aims
This study aimed to examine the risk of T1D, major depressive disorder (MDD), attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), in first-degree relatives (FDRs) of patients with T1D.
Methods
We enrolled 24,555 FDRs of individuals with T1D and 1:4 matched controls (
N
= 98,220) based on age and sex using data from the Taiwan National Health Insurance Research Database between 2001 and 2011. Poisson regression analyses were performed to estimate the risks of MDD, attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder among the FDRs. Finally, we assessed the impact of DKA in the familial coaggregation.
Results
After adjusting for demographic characteristics, FDRs of individuals with T1D had higher risk of T1D (reported as relative risk with 95% confidence interval: 46.07, 33.36–63.63) and MDD (1.17, 1.04–1.32) than controls. Stratified by sex, female FDRs had increased risk of MDD (1.30, 1.13–1.51), while male FDRs had increased risk of ADHD (1.21, 1.01–1.44). Stratified by kinship, parents of individuals with T1D had increased risk of MDD (1.24, 1.06–1.44); offspring of individuals with T1D had increased risk of ADHD (1.41, 1.11–1.79). Importantly, FDRs of individuals with T1D and DKA had higher risk of MDD (1.35, 1.11–1.64) and ADHD (1.40, 1.07–1.82) than controls; however, such risks were not observed in FDRs of individuals with T1D but without DKA.
Conclusions
The individual risks of T1D, MDD, and ADHD were increased in families that included patients with T1D, and DKA might play a role in such coaggregation with MDD and ADHD. Future studies are warranted to investigate the underlying mechanisms.</description><subject>Attention Deficit Disorder with Hyperactivity - epidemiology</subject><subject>Attention Deficit Disorder with Hyperactivity - genetics</subject><subject>Attention deficit hyperactivity disorder</subject><subject>Autism</subject><subject>Autism Spectrum Disorder - etiology</subject><subject>Autism Spectrum Disorder - genetics</subject><subject>Depressive Disorder, Major - complications</subject><subject>Depressive Disorder, Major - epidemiology</subject><subject>Depressive Disorder, Major - genetics</subject><subject>Diabetes</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Female</subject><subject>Humans</subject><subject>Hyperactivity</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mental depression</subject><subject>Metabolic Diseases</subject><subject>Original Article</subject><subject>Parents</subject><issn>1432-5233</issn><issn>0940-5429</issn><issn>1432-5233</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1TAQhiMEoqXwAiyQJTYsGvAliWN2qKIFqVI3ZR3NsScHH504weO0ysvxbDg9vSAWLCxbM9_8M-O_KN4K_lFwrj8R57WRJZfr4bIuq2fFsaiULGup1PO_3kfFK6Id50Jq1b4sjlTTKF1Lc1z8PofB7xdmR9huI24h-TGwsWdpmZAJ5jxsMCGxAfd7n2Y6ZQPsxsgcThGJ_A1mhsboMJ4ySAnDqlA67L31GOzCfmalCDb5G5-WR5hBcAzm5GlgNKFNcR6ekj4w6PscRcf6dUKP9JkBC3fz3XqHjNLsltfFix72hG_u75Pix_nX67Nv5eXVxfezL5elzXumUjita8GbWghZN41U2rai6ivRIggA3usKKjSgK6NNK1WTgxvJGzCVNa2w6qT4cNCd4vhrRkrd4MnmL4GA40yd1E2dW5imyuj7f9DdOMeQp8tUazIo5ErJA2XjSBSx76boB4hLJ3i3utsd3O2yu92du91a9O5eet4M6B5LHuzMgDoAlFNhi_Gp939k_wCbiLMv</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Hsu, Tien-Wei</creator><creator>Chen, Mu-Hong</creator><creator>Bai, Ya-Mei</creator><creator>Chang, Wen-Han</creator><creator>Cheng, Chih-Ming</creator><creator>Su, Tung-Ping</creator><creator>Chen, Tzeng-Ji</creator><creator>Tsai, Shih-Jen</creator><creator>Liang, Chih-Sung</creator><general>Springer Milan</general><general>Springer Nature B.V</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1138-5586</orcidid><orcidid>https://orcid.org/0000-0002-9987-022X</orcidid></search><sort><creationdate>20230401</creationdate><title>Family coaggregation of type 1 diabetes mellitus, major depressive disorder, attention-deficiency hyperactivity disorder and autism spectrum disorder in affected families: a nationwide study</title><author>Hsu, Tien-Wei ; Chen, Mu-Hong ; Bai, Ya-Mei ; Chang, Wen-Han ; Cheng, Chih-Ming ; Su, Tung-Ping ; Chen, Tzeng-Ji ; Tsai, Shih-Jen ; Liang, Chih-Sung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-1d7751065112566237c814f418ea1aa0f74a4e9a7497982361aab206a94c981c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Attention Deficit Disorder with Hyperactivity - epidemiology</topic><topic>Attention Deficit Disorder with Hyperactivity - genetics</topic><topic>Attention deficit hyperactivity disorder</topic><topic>Autism</topic><topic>Autism Spectrum Disorder - etiology</topic><topic>Autism Spectrum Disorder - genetics</topic><topic>Depressive Disorder, Major - complications</topic><topic>Depressive Disorder, Major - epidemiology</topic><topic>Depressive Disorder, Major - genetics</topic><topic>Diabetes</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Female</topic><topic>Humans</topic><topic>Hyperactivity</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mental depression</topic><topic>Metabolic Diseases</topic><topic>Original Article</topic><topic>Parents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsu, Tien-Wei</creatorcontrib><creatorcontrib>Chen, Mu-Hong</creatorcontrib><creatorcontrib>Bai, Ya-Mei</creatorcontrib><creatorcontrib>Chang, Wen-Han</creatorcontrib><creatorcontrib>Cheng, Chih-Ming</creatorcontrib><creatorcontrib>Su, Tung-Ping</creatorcontrib><creatorcontrib>Chen, Tzeng-Ji</creatorcontrib><creatorcontrib>Tsai, Shih-Jen</creatorcontrib><creatorcontrib>Liang, Chih-Sung</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Acta diabetologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsu, Tien-Wei</au><au>Chen, Mu-Hong</au><au>Bai, Ya-Mei</au><au>Chang, Wen-Han</au><au>Cheng, Chih-Ming</au><au>Su, Tung-Ping</au><au>Chen, Tzeng-Ji</au><au>Tsai, Shih-Jen</au><au>Liang, Chih-Sung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Family coaggregation of type 1 diabetes mellitus, major depressive disorder, attention-deficiency hyperactivity disorder and autism spectrum disorder in affected families: a nationwide study</atitle><jtitle>Acta diabetologica</jtitle><stitle>Acta Diabetol</stitle><addtitle>Acta Diabetol</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>60</volume><issue>4</issue><spage>517</spage><epage>525</epage><pages>517-525</pages><issn>1432-5233</issn><issn>0940-5429</issn><eissn>1432-5233</eissn><abstract>Aims
This study aimed to examine the risk of T1D, major depressive disorder (MDD), attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), in first-degree relatives (FDRs) of patients with T1D.
Methods
We enrolled 24,555 FDRs of individuals with T1D and 1:4 matched controls (
N
= 98,220) based on age and sex using data from the Taiwan National Health Insurance Research Database between 2001 and 2011. Poisson regression analyses were performed to estimate the risks of MDD, attention-deficiency hyperactivity disorder (ADHD), and autism spectrum disorder among the FDRs. Finally, we assessed the impact of DKA in the familial coaggregation.
Results
After adjusting for demographic characteristics, FDRs of individuals with T1D had higher risk of T1D (reported as relative risk with 95% confidence interval: 46.07, 33.36–63.63) and MDD (1.17, 1.04–1.32) than controls. Stratified by sex, female FDRs had increased risk of MDD (1.30, 1.13–1.51), while male FDRs had increased risk of ADHD (1.21, 1.01–1.44). Stratified by kinship, parents of individuals with T1D had increased risk of MDD (1.24, 1.06–1.44); offspring of individuals with T1D had increased risk of ADHD (1.41, 1.11–1.79). Importantly, FDRs of individuals with T1D and DKA had higher risk of MDD (1.35, 1.11–1.64) and ADHD (1.40, 1.07–1.82) than controls; however, such risks were not observed in FDRs of individuals with T1D but without DKA.
Conclusions
The individual risks of T1D, MDD, and ADHD were increased in families that included patients with T1D, and DKA might play a role in such coaggregation with MDD and ADHD. Future studies are warranted to investigate the underlying mechanisms.</abstract><cop>Milan</cop><pub>Springer Milan</pub><pmid>36637529</pmid><doi>10.1007/s00592-022-02025-4</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1138-5586</orcidid><orcidid>https://orcid.org/0000-0002-9987-022X</orcidid></addata></record> |
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subjects | Attention Deficit Disorder with Hyperactivity - epidemiology Attention Deficit Disorder with Hyperactivity - genetics Attention deficit hyperactivity disorder Autism Autism Spectrum Disorder - etiology Autism Spectrum Disorder - genetics Depressive Disorder, Major - complications Depressive Disorder, Major - epidemiology Depressive Disorder, Major - genetics Diabetes Diabetes mellitus (insulin dependent) Diabetes Mellitus, Type 1 - complications Female Humans Hyperactivity Internal Medicine Male Medicine Medicine & Public Health Mental depression Metabolic Diseases Original Article Parents |
title | Family coaggregation of type 1 diabetes mellitus, major depressive disorder, attention-deficiency hyperactivity disorder and autism spectrum disorder in affected families: a nationwide study |
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