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Skin intrinsic fluorescence scores are a predictor of all-cause mortality risk in type 1 diabetes: The Epidemiology of Diabetes Complications study
We assessed the association of skin intrinsic fluorescence (SIF) scores, as a measure of advanced glycation end-products (AGE), with all-cause mortality in type 1 diabetes (T1D). This is an observational retrospective study of a convenience sample from the Epidemiology of Diabetes Complications (EDC...
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Published in: | Journal of diabetes and its complications 2021-02, Vol.35 (2), p.107770-107770, Article 107770 |
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description | We assessed the association of skin intrinsic fluorescence (SIF) scores, as a measure of advanced glycation end-products (AGE), with all-cause mortality in type 1 diabetes (T1D).
This is an observational retrospective study of a convenience sample from the Epidemiology of Diabetes Complications (EDC) study. AGEs were measured with a SIF score between 2007 and 2014; vital status was assessed in 2020.
Among 245 participants, mean age was 48.6 ± 7.4 years, median diabetes duration was 39.5 years (IQR: 34.2, 44.9), and 53.5% were female. Compared to survivors, the deceased (n = 20) were older, with higher SIF scores, longer diabetes duration, lower body mass index (BMI), and an adverse risk factor profile (all p≤0.05). Univariate Cox regression showed a marginal association between SIF score and mortality (HR: 1.1, 95% CI 0.9–1.2, p = 0.06), which persisted after adjustment for multiple daily insulin shots/pump (MDI) use (HR: 1.1, 95% CI 1.0–1.2, p = 0.04). This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate (eGFR).
In individuals with long duration T1D, SIF scores adjusted for MDI predicted all-cause mortality, although this association was attenuated after adjustments. Given the nature of sampling and small number of events, our findings require replication.
•AGE accumulation is particularly harmful for patients with T1D and have been associated with mortality in T1D.•We sought to identify the relationship between collagen-linked AGE, assessed via SIF scores, and all-cause mortality in T1D.•We found a marginal association between skin intrinsic fluorescence score and mortality which persisted after adjustment for multiple daily insulin shots/pump use.•This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate.•Our work also demonstrates that non-invasive SIF scores provide a novel approach for monitoring the role of AGEs in T1D. |
doi_str_mv | 10.1016/j.jdiacomp.2020.107770 |
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This is an observational retrospective study of a convenience sample from the Epidemiology of Diabetes Complications (EDC) study. AGEs were measured with a SIF score between 2007 and 2014; vital status was assessed in 2020.
Among 245 participants, mean age was 48.6 ± 7.4 years, median diabetes duration was 39.5 years (IQR: 34.2, 44.9), and 53.5% were female. Compared to survivors, the deceased (n = 20) were older, with higher SIF scores, longer diabetes duration, lower body mass index (BMI), and an adverse risk factor profile (all p≤0.05). Univariate Cox regression showed a marginal association between SIF score and mortality (HR: 1.1, 95% CI 0.9–1.2, p = 0.06), which persisted after adjustment for multiple daily insulin shots/pump (MDI) use (HR: 1.1, 95% CI 1.0–1.2, p = 0.04). This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate (eGFR).
In individuals with long duration T1D, SIF scores adjusted for MDI predicted all-cause mortality, although this association was attenuated after adjustments. Given the nature of sampling and small number of events, our findings require replication.
•AGE accumulation is particularly harmful for patients with T1D and have been associated with mortality in T1D.•We sought to identify the relationship between collagen-linked AGE, assessed via SIF scores, and all-cause mortality in T1D.•We found a marginal association between skin intrinsic fluorescence score and mortality which persisted after adjustment for multiple daily insulin shots/pump use.•This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate.•Our work also demonstrates that non-invasive SIF scores provide a novel approach for monitoring the role of AGEs in T1D.</description><identifier>ISSN: 1056-8727</identifier><identifier>EISSN: 1873-460X</identifier><identifier>DOI: 10.1016/j.jdiacomp.2020.107770</identifier><identifier>PMID: 33168396</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Age ; All-cause mortality ; Blood ; Cholesterol ; Chromatography ; Collagen ; Creatinine ; Devices ; Diabetes ; Diabetes Complications ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - epidemiology ; Epidemiology ; Female ; Fluorescence ; Glycation End Products, Advanced - analysis ; Glycation/AGE ; Hemoglobin ; Humans ; Insulin resistance ; Life expectancy ; Light emitting diodes ; Male ; Middle Aged ; Mortality ; Retrospective Studies ; Risk Factors ; Skin ; Skin - diagnostic imaging ; Skin intrinsic fluorescence ; Type 1 diabetes</subject><ispartof>Journal of diabetes and its complications, 2021-02, Vol.35 (2), p.107770-107770, Article 107770</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><rights>2020. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-fa8c61e5431b45133c4d9de2e8a9df97176097b06f30402a72cbb766c5c60cb53</citedby><cites>FETCH-LOGICAL-c499t-fa8c61e5431b45133c4d9de2e8a9df97176097b06f30402a72cbb766c5c60cb53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33168396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tomaszewski, Erin L.</creatorcontrib><creatorcontrib>Orchard, Trevor J.</creatorcontrib><creatorcontrib>Hawkins, Marquis</creatorcontrib><creatorcontrib>Conway, Baqiyyah N.</creatorcontrib><creatorcontrib>Buchanich, Jeanine M.</creatorcontrib><creatorcontrib>Maynard, John</creatorcontrib><creatorcontrib>Songer, Thomas</creatorcontrib><creatorcontrib>Costacou, Tina</creatorcontrib><title>Skin intrinsic fluorescence scores are a predictor of all-cause mortality risk in type 1 diabetes: The Epidemiology of Diabetes Complications study</title><title>Journal of diabetes and its complications</title><addtitle>J Diabetes Complications</addtitle><description>We assessed the association of skin intrinsic fluorescence (SIF) scores, as a measure of advanced glycation end-products (AGE), with all-cause mortality in type 1 diabetes (T1D).
This is an observational retrospective study of a convenience sample from the Epidemiology of Diabetes Complications (EDC) study. AGEs were measured with a SIF score between 2007 and 2014; vital status was assessed in 2020.
Among 245 participants, mean age was 48.6 ± 7.4 years, median diabetes duration was 39.5 years (IQR: 34.2, 44.9), and 53.5% were female. Compared to survivors, the deceased (n = 20) were older, with higher SIF scores, longer diabetes duration, lower body mass index (BMI), and an adverse risk factor profile (all p≤0.05). Univariate Cox regression showed a marginal association between SIF score and mortality (HR: 1.1, 95% CI 0.9–1.2, p = 0.06), which persisted after adjustment for multiple daily insulin shots/pump (MDI) use (HR: 1.1, 95% CI 1.0–1.2, p = 0.04). This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate (eGFR).
In individuals with long duration T1D, SIF scores adjusted for MDI predicted all-cause mortality, although this association was attenuated after adjustments. Given the nature of sampling and small number of events, our findings require replication.
•AGE accumulation is particularly harmful for patients with T1D and have been associated with mortality in T1D.•We sought to identify the relationship between collagen-linked AGE, assessed via SIF scores, and all-cause mortality in T1D.•We found a marginal association between skin intrinsic fluorescence score and mortality which persisted after adjustment for multiple daily insulin shots/pump use.•This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate.•Our work also demonstrates that non-invasive SIF scores provide a novel approach for monitoring the role of AGEs in T1D.</description><subject>Adult</subject><subject>Age</subject><subject>All-cause mortality</subject><subject>Blood</subject><subject>Cholesterol</subject><subject>Chromatography</subject><subject>Collagen</subject><subject>Creatinine</subject><subject>Devices</subject><subject>Diabetes</subject><subject>Diabetes Complications</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - epidemiology</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Glycation End Products, Advanced - analysis</subject><subject>Glycation/AGE</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Life expectancy</subject><subject>Light emitting diodes</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Skin</subject><subject>Skin - diagnostic imaging</subject><subject>Skin intrinsic fluorescence</subject><subject>Type 1 diabetes</subject><issn>1056-8727</issn><issn>1873-460X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1TAQhSMEoqXwCpUlNmxysePYTlgg0KX8SJVYUCR2lmNPWqdOHGynUp6DF8bRva2ADSuPPJ-P58wpinOCdwQT_nrYDcYq7cd5V-FquxRC4EfFKWkELWuOfzzONWa8bEQlTopnMQ4YY84YeVqcUEp4Q1t-Wvz6dmsnZKcU7BStRr1bfICoYdKAot5qpAIgheYAxurkA_I9Us6VWi0R0OhDUs6mFQUbb7MSSusMiKA8XgcJ4ht0dQPoYrYGRuudv143gQ_HLtpnC85qlayfIoppMevz4kmvXIQXx_Os-P7x4mr_ubz8-unL_v1lqeu2TWWvGs0JsJqSrmaEUl2b1kAFjWpN3woiOG5Fh3lPcY0rJSrddYJzzTTHumP0rHh70J2XbgSTPaegnJyDHVVYpVdW_t2Z7I289ndSNIw1tcgCr44Cwf9cICY52rw659QEfomyqllL65Y2PKMv_0EHv4Qp28uU4LSqcjiZ4gdKBx9jgP5hGILllrsc5H3ucstdHnLPD8__tPLw7D7oDLw7AJAXemchyKjtFrKxAXSSxtv__fEbt47FPQ</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Tomaszewski, Erin L.</creator><creator>Orchard, Trevor J.</creator><creator>Hawkins, Marquis</creator><creator>Conway, Baqiyyah N.</creator><creator>Buchanich, Jeanine M.</creator><creator>Maynard, John</creator><creator>Songer, Thomas</creator><creator>Costacou, Tina</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K6X</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210201</creationdate><title>Skin intrinsic fluorescence scores are a predictor of all-cause mortality risk in type 1 diabetes: The Epidemiology of Diabetes Complications study</title><author>Tomaszewski, Erin L. ; Orchard, Trevor J. ; Hawkins, Marquis ; Conway, Baqiyyah N. ; Buchanich, Jeanine M. ; Maynard, John ; Songer, Thomas ; Costacou, Tina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-fa8c61e5431b45133c4d9de2e8a9df97176097b06f30402a72cbb766c5c60cb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Age</topic><topic>All-cause mortality</topic><topic>Blood</topic><topic>Cholesterol</topic><topic>Chromatography</topic><topic>Collagen</topic><topic>Creatinine</topic><topic>Devices</topic><topic>Diabetes</topic><topic>Diabetes Complications</topic><topic>Diabetes Mellitus, Type 1 - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of diabetes and its complications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomaszewski, Erin L.</au><au>Orchard, Trevor J.</au><au>Hawkins, Marquis</au><au>Conway, Baqiyyah N.</au><au>Buchanich, Jeanine M.</au><au>Maynard, John</au><au>Songer, Thomas</au><au>Costacou, Tina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skin intrinsic fluorescence scores are a predictor of all-cause mortality risk in type 1 diabetes: The Epidemiology of Diabetes Complications study</atitle><jtitle>Journal of diabetes and its complications</jtitle><addtitle>J Diabetes Complications</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>35</volume><issue>2</issue><spage>107770</spage><epage>107770</epage><pages>107770-107770</pages><artnum>107770</artnum><issn>1056-8727</issn><eissn>1873-460X</eissn><abstract>We assessed the association of skin intrinsic fluorescence (SIF) scores, as a measure of advanced glycation end-products (AGE), with all-cause mortality in type 1 diabetes (T1D).
This is an observational retrospective study of a convenience sample from the Epidemiology of Diabetes Complications (EDC) study. AGEs were measured with a SIF score between 2007 and 2014; vital status was assessed in 2020.
Among 245 participants, mean age was 48.6 ± 7.4 years, median diabetes duration was 39.5 years (IQR: 34.2, 44.9), and 53.5% were female. Compared to survivors, the deceased (n = 20) were older, with higher SIF scores, longer diabetes duration, lower body mass index (BMI), and an adverse risk factor profile (all p≤0.05). Univariate Cox regression showed a marginal association between SIF score and mortality (HR: 1.1, 95% CI 0.9–1.2, p = 0.06), which persisted after adjustment for multiple daily insulin shots/pump (MDI) use (HR: 1.1, 95% CI 1.0–1.2, p = 0.04). This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate (eGFR).
In individuals with long duration T1D, SIF scores adjusted for MDI predicted all-cause mortality, although this association was attenuated after adjustments. Given the nature of sampling and small number of events, our findings require replication.
•AGE accumulation is particularly harmful for patients with T1D and have been associated with mortality in T1D.•We sought to identify the relationship between collagen-linked AGE, assessed via SIF scores, and all-cause mortality in T1D.•We found a marginal association between skin intrinsic fluorescence score and mortality which persisted after adjustment for multiple daily insulin shots/pump use.•This association was attenuated after adjustment for T1D duration, A1c months, or estimated glomerular filtration rate.•Our work also demonstrates that non-invasive SIF scores provide a novel approach for monitoring the role of AGEs in T1D.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33168396</pmid><doi>10.1016/j.jdiacomp.2020.107770</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Age All-cause mortality Blood Cholesterol Chromatography Collagen Creatinine Devices Diabetes Diabetes Complications Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - epidemiology Epidemiology Female Fluorescence Glycation End Products, Advanced - analysis Glycation/AGE Hemoglobin Humans Insulin resistance Life expectancy Light emitting diodes Male Middle Aged Mortality Retrospective Studies Risk Factors Skin Skin - diagnostic imaging Skin intrinsic fluorescence Type 1 diabetes |
title | Skin intrinsic fluorescence scores are a predictor of all-cause mortality risk in type 1 diabetes: The Epidemiology of Diabetes Complications study |
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