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The angiotensin I-converting enzyme (ACE) locus is strongly associated with age and duration of diabetes in patients with Type I diabetes
We have investigated the frequency of the angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism in 249 patients with type I diabetes and 162 normal healthy controls. There was no significant difference in the frequency of ACE genotypes between those patients with diabetic nephr...
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Published in: | Journal of diabetes and its complications 1997, Vol.11 (1), p.2-8 |
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container_title | Journal of diabetes and its complications |
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creator | Hibberd, M.L. Millward, B.A. Demaine, A.G. |
description | We have investigated the frequency of the angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism in 249 patients with type I diabetes and 162 normal healthy controls. There was no significant difference in the frequency of ACE genotypes between those patients with diabetic nephropathy (
n = 72) (nephropaths) compared to those with no proteinuria after 20 years duration of diabetes (
n = 86) (normoalbuminurics). There was, however, a significant difference in the frequency of ACE genotypes between the short-duration and long-term normoalbuminuric group (
χ = 11.5,
p = 0.001). Analysis of the ACE genotypes with respect to age and duration of diabetes showed that homozygosity for the insertion (I/I) genotype was significantly decreased with longer duration of diabetes (
r
2 = 92.7%,
p < 0.009). No association was found with age in the normal controls. In conclusion, these results suggest that the ACE locus may be associated with longevity and survival in patients with type I diabetes rather than diabetic nephropathy or microvascular disease per se. |
doi_str_mv | 10.1016/1056-8727(95)00114-X |
format | article |
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n = 72) (nephropaths) compared to those with no proteinuria after 20 years duration of diabetes (
n = 86) (normoalbuminurics). There was, however, a significant difference in the frequency of ACE genotypes between the short-duration and long-term normoalbuminuric group (
χ = 11.5,
p = 0.001). Analysis of the ACE genotypes with respect to age and duration of diabetes showed that homozygosity for the insertion (I/I) genotype was significantly decreased with longer duration of diabetes (
r
2 = 92.7%,
p < 0.009). No association was found with age in the normal controls. In conclusion, these results suggest that the ACE locus may be associated with longevity and survival in patients with type I diabetes rather than diabetic nephropathy or microvascular disease per se.</description><identifier>ISSN: 1056-8727</identifier><identifier>EISSN: 1873-460X</identifier><identifier>DOI: 10.1016/1056-8727(95)00114-X</identifier><identifier>PMID: 9025006</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Age Factors ; Associated diseases and complications ; Biological and medical sciences ; Cohort Studies ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - enzymology ; Diabetes Mellitus, Type 1 - genetics ; Diabetes. Impaired glucose tolerance ; Diabetic Nephropathies - enzymology ; Diabetic Nephropathies - genetics ; Diabetic Neuropathies - enzymology ; Diabetic Neuropathies - genetics ; Diabetic Retinopathy - enzymology ; Diabetic Retinopathy - genetics ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Female ; Gene Frequency ; Genotype ; Humans ; Male ; Medical sciences ; Middle Aged ; Peptidyl-Dipeptidase A - classification ; Peptidyl-Dipeptidase A - genetics ; Proteinuria - enzymology ; Proteinuria - genetics ; Sex Characteristics ; Time Factors</subject><ispartof>Journal of diabetes and its complications, 1997, Vol.11 (1), p.2-8</ispartof><rights>1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-fbf6ac617488fc6da05d7a22ee65992ab2e01960a2de7aa48222bf6aa41fa3333</citedby><cites>FETCH-LOGICAL-c386t-fbf6ac617488fc6da05d7a22ee65992ab2e01960a2de7aa48222bf6aa41fa3333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2566361$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9025006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hibberd, M.L.</creatorcontrib><creatorcontrib>Millward, B.A.</creatorcontrib><creatorcontrib>Demaine, A.G.</creatorcontrib><title>The angiotensin I-converting enzyme (ACE) locus is strongly associated with age and duration of diabetes in patients with Type I diabetes</title><title>Journal of diabetes and its complications</title><addtitle>J Diabetes Complications</addtitle><description>We have investigated the frequency of the angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism in 249 patients with type I diabetes and 162 normal healthy controls. There was no significant difference in the frequency of ACE genotypes between those patients with diabetic nephropathy (
n = 72) (nephropaths) compared to those with no proteinuria after 20 years duration of diabetes (
n = 86) (normoalbuminurics). There was, however, a significant difference in the frequency of ACE genotypes between the short-duration and long-term normoalbuminuric group (
χ = 11.5,
p = 0.001). Analysis of the ACE genotypes with respect to age and duration of diabetes showed that homozygosity for the insertion (I/I) genotype was significantly decreased with longer duration of diabetes (
r
2 = 92.7%,
p < 0.009). No association was found with age in the normal controls. In conclusion, these results suggest that the ACE locus may be associated with longevity and survival in patients with type I diabetes rather than diabetic nephropathy or microvascular disease per se.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Associated diseases and complications</subject><subject>Biological and medical sciences</subject><subject>Cohort Studies</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - enzymology</subject><subject>Diabetes Mellitus, Type 1 - genetics</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diabetic Nephropathies - enzymology</subject><subject>Diabetic Nephropathies - genetics</subject><subject>Diabetic Neuropathies - enzymology</subject><subject>Diabetic Neuropathies - genetics</subject><subject>Diabetic Retinopathy - enzymology</subject><subject>Diabetic Retinopathy - genetics</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Peptidyl-Dipeptidase A - classification</subject><subject>Peptidyl-Dipeptidase A - genetics</subject><subject>Proteinuria - enzymology</subject><subject>Proteinuria - genetics</subject><subject>Sex Characteristics</subject><subject>Time Factors</subject><issn>1056-8727</issn><issn>1873-460X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNp9kcFuEzEQhi0EKm3hDUDyAaH2sGA7a-_upVIVFYhUiUuQcrMm9mxqtLGD7S0Kb8Bb19uEHPHFHs_3_7b-IeQdZ5844-ozZ1JVbSOaq05eM8Z5Xa1ekHPeNrOqVmz1spz_Ia_JRUo_GWNKSn5GzjomZCnOyd_lA1LwGxcy-uQ8XVQm-EeM2fkNRf9nv0V6dTu_u6ZDMGOiLtGUY_CbYU8hpWAcZLT0t8sPFDaTl6V2jJBd8DT01DpYY8Yi9HRXbtHndKCX-x3SxQl4Q171MCR8e9wvyY8vd8v5t-r--9fF_Pa-MrNW5apf9wqM4k3dtr1RFpi0DQiBqGTXCVgLZLxTDITFBqBuhRCTBGrew6ysS_Lx4LuL4deIKeutSwaHATyGMemmbUXTKV7A-gCaGFKK2OtddFuIe82Zniagp3j1FK_upH6egF4V2fuj_7jeoj2JjpGX_odjH5KBoY_gjUsnTEilZs-v3xwwLFk8Oow6mRKeQesimqxtcP__xxPXyqPf</recordid><startdate>1997</startdate><enddate>1997</enddate><creator>Hibberd, M.L.</creator><creator>Millward, B.A.</creator><creator>Demaine, A.G.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>1997</creationdate><title>The angiotensin I-converting enzyme (ACE) locus is strongly associated with age and duration of diabetes in patients with Type I diabetes</title><author>Hibberd, M.L. ; Millward, B.A. ; Demaine, A.G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-fbf6ac617488fc6da05d7a22ee65992ab2e01960a2de7aa48222bf6aa41fa3333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Associated diseases and complications</topic><topic>Biological and medical sciences</topic><topic>Cohort Studies</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Diabetes Mellitus, Type 1 - enzymology</topic><topic>Diabetes Mellitus, Type 1 - genetics</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diabetic Nephropathies - enzymology</topic><topic>Diabetic Nephropathies - genetics</topic><topic>Diabetic Neuropathies - enzymology</topic><topic>Diabetic Neuropathies - genetics</topic><topic>Diabetic Retinopathy - enzymology</topic><topic>Diabetic Retinopathy - genetics</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Peptidyl-Dipeptidase A - classification</topic><topic>Peptidyl-Dipeptidase A - genetics</topic><topic>Proteinuria - enzymology</topic><topic>Proteinuria - genetics</topic><topic>Sex Characteristics</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hibberd, M.L.</creatorcontrib><creatorcontrib>Millward, B.A.</creatorcontrib><creatorcontrib>Demaine, A.G.</creatorcontrib><collection>Pascal-Francis</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><jtitle>Journal of diabetes and its complications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hibberd, M.L.</au><au>Millward, B.A.</au><au>Demaine, A.G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The angiotensin I-converting enzyme (ACE) locus is strongly associated with age and duration of diabetes in patients with Type I diabetes</atitle><jtitle>Journal of diabetes and its complications</jtitle><addtitle>J Diabetes Complications</addtitle><date>1997</date><risdate>1997</risdate><volume>11</volume><issue>1</issue><spage>2</spage><epage>8</epage><pages>2-8</pages><issn>1056-8727</issn><eissn>1873-460X</eissn><abstract>We have investigated the frequency of the angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism in 249 patients with type I diabetes and 162 normal healthy controls. There was no significant difference in the frequency of ACE genotypes between those patients with diabetic nephropathy (
n = 72) (nephropaths) compared to those with no proteinuria after 20 years duration of diabetes (
n = 86) (normoalbuminurics). There was, however, a significant difference in the frequency of ACE genotypes between the short-duration and long-term normoalbuminuric group (
χ = 11.5,
p = 0.001). Analysis of the ACE genotypes with respect to age and duration of diabetes showed that homozygosity for the insertion (I/I) genotype was significantly decreased with longer duration of diabetes (
r
2 = 92.7%,
p < 0.009). No association was found with age in the normal controls. In conclusion, these results suggest that the ACE locus may be associated with longevity and survival in patients with type I diabetes rather than diabetic nephropathy or microvascular disease per se.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>9025006</pmid><doi>10.1016/1056-8727(95)00114-X</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Age Factors Associated diseases and complications Biological and medical sciences Cohort Studies Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - enzymology Diabetes Mellitus, Type 1 - genetics Diabetes. Impaired glucose tolerance Diabetic Nephropathies - enzymology Diabetic Nephropathies - genetics Diabetic Neuropathies - enzymology Diabetic Neuropathies - genetics Diabetic Retinopathy - enzymology Diabetic Retinopathy - genetics Endocrine pancreas. Apud cells (diseases) Endocrinopathies Female Gene Frequency Genotype Humans Male Medical sciences Middle Aged Peptidyl-Dipeptidase A - classification Peptidyl-Dipeptidase A - genetics Proteinuria - enzymology Proteinuria - genetics Sex Characteristics Time Factors |
title | The angiotensin I-converting enzyme (ACE) locus is strongly associated with age and duration of diabetes in patients with Type I diabetes |
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