Comparison of cystatin C- and creatinine-based estimated glomerular filtration rates for predicting all-cause mortality in Japanese patients with type 2 diabetes: the Fukuoka Diabetes Registry

Background There is little information about the predictive ability of cystatin C-based estimated glomerular filtration rates (eGFR Cys ) for all-cause mortality in Asian populations. We compared the discriminatory ability of eGFR Cys for all-cause mortality with that of creatinine-based estimated g...

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Veröffentlicht in:Clinical and experimental nephrology 2017-06, Vol.21 (3), p.383-390
Hauptverfasser: Ide, Hitoshi, Iwase, Masanori, Fujii, Hiroki, Ohkuma, Toshiaki, Kaizu, Shinako, Jodai, Tamaki, Kikuchi, Yohei, Idewaki, Yasuhiro, Sumi, Akiko, Nakamura, Udai, Kitazono, Takanari
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container_issue 3
container_start_page 383
container_title Clinical and experimental nephrology
container_volume 21
creator Ide, Hitoshi
Iwase, Masanori
Fujii, Hiroki
Ohkuma, Toshiaki
Kaizu, Shinako
Jodai, Tamaki
Kikuchi, Yohei
Idewaki, Yasuhiro
Sumi, Akiko
Nakamura, Udai
Kitazono, Takanari
description Background There is little information about the predictive ability of cystatin C-based estimated glomerular filtration rates (eGFR Cys ) for all-cause mortality in Asian populations. We compared the discriminatory ability of eGFR Cys for all-cause mortality with that of creatinine-based estimated glomerular filtration rates (eGFR Cr ) in Japanese patients with type 2 diabetes. Methods A total of 4869 participants were classified into four categories (eGFR ≤29, 30–59, 60–89, and ≥90 ml/min/1.73 m 2 ) by eGFR Cr and eGFR Cys , and followed up for a median of 3.3 years. Results 150 deaths were identified. The multivariable-adjusted risk of all-cause mortality was significantly increased in eGFR Cr  ≤29 ml/min/1.73 m 2 compared with eGFR Cr  ≥90 ml/min/1.73 m 2 [hazard ratio (HR) 2.4 (95 % confidence interval (95 % CI) 1.2–5.0)], whereas it was significantly increased in eGFR Cys 59 ml/min/1.73 m 2 or lower [30–59 ml/min/1.73 m 2 , HR 1.9 (95 % CI 1.1–3.5); ≤29 ml/min/1.73 m 2 , HR 5.8 (95 % CI 2.8–12.0)]. Comparing eGFR Cys with eGFR Cr , the proportions of participants reclassified to lower and higher eGFR stages were 6.3 and 28.8 %, respectively. The multivariable-adjusted HRs for all-cause mortality were 1.8 (95 % CI 1.1–2.9) and 0.7 (95 % CI 0.4–1.1), respectively. The C statistic of the model including eGFR Cys and other risk factors was significantly increased compared with the model including eGFR Cr . The net reclassification improvement and the integrated discrimination improvement were significantly positive. Conclusions Our findings suggest that eGFR Cys has a stronger association with all-cause mortality and is superior to eGFR Cr for predicting all-cause mortality in Japanese patients with type 2 diabetes.
doi_str_mv 10.1007/s10157-016-1296-2
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We compared the discriminatory ability of eGFR Cys for all-cause mortality with that of creatinine-based estimated glomerular filtration rates (eGFR Cr ) in Japanese patients with type 2 diabetes. Methods A total of 4869 participants were classified into four categories (eGFR ≤29, 30–59, 60–89, and ≥90 ml/min/1.73 m 2 ) by eGFR Cr and eGFR Cys , and followed up for a median of 3.3 years. Results 150 deaths were identified. The multivariable-adjusted risk of all-cause mortality was significantly increased in eGFR Cr  ≤29 ml/min/1.73 m 2 compared with eGFR Cr  ≥90 ml/min/1.73 m 2 [hazard ratio (HR) 2.4 (95 % confidence interval (95 % CI) 1.2–5.0)], whereas it was significantly increased in eGFR Cys 59 ml/min/1.73 m 2 or lower [30–59 ml/min/1.73 m 2 , HR 1.9 (95 % CI 1.1–3.5); ≤29 ml/min/1.73 m 2 , HR 5.8 (95 % CI 2.8–12.0)]. Comparing eGFR Cys with eGFR Cr , the proportions of participants reclassified to lower and higher eGFR stages were 6.3 and 28.8 %, respectively. The multivariable-adjusted HRs for all-cause mortality were 1.8 (95 % CI 1.1–2.9) and 0.7 (95 % CI 0.4–1.1), respectively. The C statistic of the model including eGFR Cys and other risk factors was significantly increased compared with the model including eGFR Cr . The net reclassification improvement and the integrated discrimination improvement were significantly positive. Conclusions Our findings suggest that eGFR Cys has a stronger association with all-cause mortality and is superior to eGFR Cr for predicting all-cause mortality in Japanese patients with type 2 diabetes.</description><identifier>ISSN: 1342-1751</identifier><identifier>EISSN: 1437-7799</identifier><identifier>DOI: 10.1007/s10157-016-1296-2</identifier><identifier>PMID: 27339449</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Aged ; Asian Continental Ancestry Group ; Beta blockers ; Biomarkers - blood ; Cause of Death ; Chi-Square Distribution ; Creatinine ; Creatinine - blood ; Cystatin C ; Cystatin C - blood ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Type 2 - diagnosis ; Diabetes Mellitus, Type 2 - ethnology ; Diabetes Mellitus, Type 2 - mortality ; Diabetic Nephropathies - diagnosis ; Diabetic Nephropathies - ethnology ; Diabetic Nephropathies - mortality ; Diabetic Nephropathies - physiopathology ; Epidermal growth factor receptors ; Female ; Glomerular Filtration Rate ; Health risk assessment ; Humans ; Japan - epidemiology ; Kidney - physiopathology ; Linear Models ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Models, Biological ; Mortality ; Multivariate Analysis ; Nephrology ; Original Article ; Predictive Value of Tests ; Prognosis ; Proportional Hazards Models ; Prospective Studies ; Reclassification ; Registries ; Risk Factors ; Time Factors ; Urology</subject><ispartof>Clinical and experimental nephrology, 2017-06, Vol.21 (3), p.383-390</ispartof><rights>Japanese Society of Nephrology 2016</rights><rights>Clinical and Experimental Nephrology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c578t-9a08514e9f85204e3fb9d7039f789b99951cdfc069da1ca323547b0e9fbc28963</citedby><cites>FETCH-LOGICAL-c578t-9a08514e9f85204e3fb9d7039f789b99951cdfc069da1ca323547b0e9fbc28963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10157-016-1296-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10157-016-1296-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27339449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ide, Hitoshi</creatorcontrib><creatorcontrib>Iwase, Masanori</creatorcontrib><creatorcontrib>Fujii, Hiroki</creatorcontrib><creatorcontrib>Ohkuma, Toshiaki</creatorcontrib><creatorcontrib>Kaizu, Shinako</creatorcontrib><creatorcontrib>Jodai, Tamaki</creatorcontrib><creatorcontrib>Kikuchi, Yohei</creatorcontrib><creatorcontrib>Idewaki, Yasuhiro</creatorcontrib><creatorcontrib>Sumi, Akiko</creatorcontrib><creatorcontrib>Nakamura, Udai</creatorcontrib><creatorcontrib>Kitazono, Takanari</creatorcontrib><title>Comparison of cystatin C- and creatinine-based estimated glomerular filtration rates for predicting all-cause mortality in Japanese patients with type 2 diabetes: the Fukuoka Diabetes Registry</title><title>Clinical and experimental nephrology</title><addtitle>Clin Exp Nephrol</addtitle><addtitle>Clin Exp Nephrol</addtitle><description>Background There is little information about the predictive ability of cystatin C-based estimated glomerular filtration rates (eGFR Cys ) for all-cause mortality in Asian populations. We compared the discriminatory ability of eGFR Cys for all-cause mortality with that of creatinine-based estimated glomerular filtration rates (eGFR Cr ) in Japanese patients with type 2 diabetes. Methods A total of 4869 participants were classified into four categories (eGFR ≤29, 30–59, 60–89, and ≥90 ml/min/1.73 m 2 ) by eGFR Cr and eGFR Cys , and followed up for a median of 3.3 years. Results 150 deaths were identified. The multivariable-adjusted risk of all-cause mortality was significantly increased in eGFR Cr  ≤29 ml/min/1.73 m 2 compared with eGFR Cr  ≥90 ml/min/1.73 m 2 [hazard ratio (HR) 2.4 (95 % confidence interval (95 % CI) 1.2–5.0)], whereas it was significantly increased in eGFR Cys 59 ml/min/1.73 m 2 or lower [30–59 ml/min/1.73 m 2 , HR 1.9 (95 % CI 1.1–3.5); ≤29 ml/min/1.73 m 2 , HR 5.8 (95 % CI 2.8–12.0)]. Comparing eGFR Cys with eGFR Cr , the proportions of participants reclassified to lower and higher eGFR stages were 6.3 and 28.8 %, respectively. The multivariable-adjusted HRs for all-cause mortality were 1.8 (95 % CI 1.1–2.9) and 0.7 (95 % CI 0.4–1.1), respectively. The C statistic of the model including eGFR Cys and other risk factors was significantly increased compared with the model including eGFR Cr . The net reclassification improvement and the integrated discrimination improvement were significantly positive. Conclusions Our findings suggest that eGFR Cys has a stronger association with all-cause mortality and is superior to eGFR Cr for predicting all-cause mortality in Japanese patients with type 2 diabetes.</description><subject>Aged</subject><subject>Asian Continental Ancestry Group</subject><subject>Beta blockers</subject><subject>Biomarkers - blood</subject><subject>Cause of Death</subject><subject>Chi-Square Distribution</subject><subject>Creatinine</subject><subject>Creatinine - blood</subject><subject>Cystatin C</subject><subject>Cystatin C - blood</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Type 2 - diagnosis</subject><subject>Diabetes Mellitus, Type 2 - ethnology</subject><subject>Diabetes Mellitus, Type 2 - mortality</subject><subject>Diabetic Nephropathies - diagnosis</subject><subject>Diabetic Nephropathies - ethnology</subject><subject>Diabetic Nephropathies - mortality</subject><subject>Diabetic Nephropathies - physiopathology</subject><subject>Epidermal growth factor receptors</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Japan - epidemiology</subject><subject>Kidney - physiopathology</subject><subject>Linear Models</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Models, Biological</subject><subject>Mortality</subject><subject>Multivariate Analysis</subject><subject>Nephrology</subject><subject>Original Article</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Reclassification</subject><subject>Registries</subject><subject>Risk Factors</subject><subject>Time Factors</subject><subject>Urology</subject><issn>1342-1751</issn><issn>1437-7799</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kV2L1TAQhoso7of-AG9kwBtvokn6kcY7ObqrsiCIXoc0nZ7NbtvUJEX67_xpzuEcRQSvZjJ55p1k3qJ4Jvgrwbl6nQQXtWJcNExI3TD5oDgXVamYUlo_pLysJBOqFmfFRUp3nPNW1_pxcSZVWeqq0ufFz12YFht9CjOEAdyWss1-hh0DO_fgIh6OfkbW2YQ9YMp-spmy_RgmjOtoIwx-zJE40qCACYYQYYnYe0fNe7DjyJxdE8IUYrajzxvQjE92sTNSdaFenHOCHz7fQt4WBAm9tx2S2BvItwhX6_0a7i28O1XhC-59ynF7Ujwa7Jjw6SleFt-u3n_dfWA3n68_7t7eMFerNjNteVuLCvXQ1pJXWA6d7hUv9aBa3Wmta-H6wfFG91Y4W8qyrlTHie-cbHVTXhYvj7pLDN9XWoOZfHI4jvSFsCYjWtmQnuCK0Bf_oHdhjTO9zgjNlSJUtESJI-ViSCniYJZIq42bEdwc7DVHew3Zaw72Gkk9z0_Kazdh_6fjt58EyCOQ6GreY_xr9H9VfwE8aLN8</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Ide, Hitoshi</creator><creator>Iwase, Masanori</creator><creator>Fujii, Hiroki</creator><creator>Ohkuma, Toshiaki</creator><creator>Kaizu, Shinako</creator><creator>Jodai, Tamaki</creator><creator>Kikuchi, Yohei</creator><creator>Idewaki, Yasuhiro</creator><creator>Sumi, Akiko</creator><creator>Nakamura, Udai</creator><creator>Kitazono, Takanari</creator><general>Springer Japan</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>3V.</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20170601</creationdate><title>Comparison of cystatin C- and creatinine-based estimated glomerular filtration rates for predicting all-cause mortality in Japanese patients with type 2 diabetes: the Fukuoka Diabetes Registry</title><author>Ide, Hitoshi ; Iwase, Masanori ; Fujii, Hiroki ; Ohkuma, Toshiaki ; Kaizu, Shinako ; Jodai, Tamaki ; Kikuchi, Yohei ; Idewaki, Yasuhiro ; Sumi, Akiko ; Nakamura, Udai ; Kitazono, Takanari</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c578t-9a08514e9f85204e3fb9d7039f789b99951cdfc069da1ca323547b0e9fbc28963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Asian Continental Ancestry Group</topic><topic>Beta blockers</topic><topic>Biomarkers - blood</topic><topic>Cause of Death</topic><topic>Chi-Square Distribution</topic><topic>Creatinine</topic><topic>Creatinine - blood</topic><topic>Cystatin C</topic><topic>Cystatin C - blood</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Type 2 - diagnosis</topic><topic>Diabetes Mellitus, Type 2 - ethnology</topic><topic>Diabetes Mellitus, Type 2 - mortality</topic><topic>Diabetic Nephropathies - diagnosis</topic><topic>Diabetic Nephropathies - ethnology</topic><topic>Diabetic Nephropathies - mortality</topic><topic>Diabetic Nephropathies - physiopathology</topic><topic>Epidermal growth factor receptors</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Japan - epidemiology</topic><topic>Kidney - physiopathology</topic><topic>Linear Models</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Models, Biological</topic><topic>Mortality</topic><topic>Multivariate Analysis</topic><topic>Nephrology</topic><topic>Original Article</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Reclassification</topic><topic>Registries</topic><topic>Risk Factors</topic><topic>Time Factors</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ide, Hitoshi</creatorcontrib><creatorcontrib>Iwase, Masanori</creatorcontrib><creatorcontrib>Fujii, Hiroki</creatorcontrib><creatorcontrib>Ohkuma, Toshiaki</creatorcontrib><creatorcontrib>Kaizu, Shinako</creatorcontrib><creatorcontrib>Jodai, Tamaki</creatorcontrib><creatorcontrib>Kikuchi, Yohei</creatorcontrib><creatorcontrib>Idewaki, Yasuhiro</creatorcontrib><creatorcontrib>Sumi, Akiko</creatorcontrib><creatorcontrib>Nakamura, Udai</creatorcontrib><creatorcontrib>Kitazono, Takanari</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>Calcium &amp; 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We compared the discriminatory ability of eGFR Cys for all-cause mortality with that of creatinine-based estimated glomerular filtration rates (eGFR Cr ) in Japanese patients with type 2 diabetes. Methods A total of 4869 participants were classified into four categories (eGFR ≤29, 30–59, 60–89, and ≥90 ml/min/1.73 m 2 ) by eGFR Cr and eGFR Cys , and followed up for a median of 3.3 years. Results 150 deaths were identified. The multivariable-adjusted risk of all-cause mortality was significantly increased in eGFR Cr  ≤29 ml/min/1.73 m 2 compared with eGFR Cr  ≥90 ml/min/1.73 m 2 [hazard ratio (HR) 2.4 (95 % confidence interval (95 % CI) 1.2–5.0)], whereas it was significantly increased in eGFR Cys 59 ml/min/1.73 m 2 or lower [30–59 ml/min/1.73 m 2 , HR 1.9 (95 % CI 1.1–3.5); ≤29 ml/min/1.73 m 2 , HR 5.8 (95 % CI 2.8–12.0)]. Comparing eGFR Cys with eGFR Cr , the proportions of participants reclassified to lower and higher eGFR stages were 6.3 and 28.8 %, respectively. The multivariable-adjusted HRs for all-cause mortality were 1.8 (95 % CI 1.1–2.9) and 0.7 (95 % CI 0.4–1.1), respectively. The C statistic of the model including eGFR Cys and other risk factors was significantly increased compared with the model including eGFR Cr . The net reclassification improvement and the integrated discrimination improvement were significantly positive. Conclusions Our findings suggest that eGFR Cys has a stronger association with all-cause mortality and is superior to eGFR Cr for predicting all-cause mortality in Japanese patients with type 2 diabetes.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>27339449</pmid><doi>10.1007/s10157-016-1296-2</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Asian Continental Ancestry Group
Beta blockers
Biomarkers - blood
Cause of Death
Chi-Square Distribution
Creatinine
Creatinine - blood
Cystatin C
Cystatin C - blood
Diabetes
Diabetes mellitus
Diabetes Mellitus, Type 2 - diagnosis
Diabetes Mellitus, Type 2 - ethnology
Diabetes Mellitus, Type 2 - mortality
Diabetic Nephropathies - diagnosis
Diabetic Nephropathies - ethnology
Diabetic Nephropathies - mortality
Diabetic Nephropathies - physiopathology
Epidermal growth factor receptors
Female
Glomerular Filtration Rate
Health risk assessment
Humans
Japan - epidemiology
Kidney - physiopathology
Linear Models
Male
Medicine
Medicine & Public Health
Middle Aged
Models, Biological
Mortality
Multivariate Analysis
Nephrology
Original Article
Predictive Value of Tests
Prognosis
Proportional Hazards Models
Prospective Studies
Reclassification
Registries
Risk Factors
Time Factors
Urology
title Comparison of cystatin C- and creatinine-based estimated glomerular filtration rates for predicting all-cause mortality in Japanese patients with type 2 diabetes: the Fukuoka Diabetes Registry
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