Immune Sensitization and Mortality in Wait-Listed Kidney Transplant Candidates
Cardiovascular mortality is the leading cause of death in ESRD. Whereas innate and adaptive immunity have established roles in cardiovascular disease, the role of humoral immunity is unknown. We conducted a retrospective cohort study in first-time adult kidney transplant candidates (N=161,308) using...
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Veröffentlicht in: | Journal of the American Society of Nephrology 2016-02, Vol.27 (2), p.570-578 |
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description | Cardiovascular mortality is the leading cause of death in ESRD. Whereas innate and adaptive immunity have established roles in cardiovascular disease, the role of humoral immunity is unknown. We conducted a retrospective cohort study in first-time adult kidney transplant candidates (N=161,308) using data from the Scientific Registry of Transplant Recipients and the Centers for Medicare and Medicaid Services to evaluate whether anti-human leukocyte antigen antibodies, measured as panel reactive antibodies (PRAs), are related to mortality in ESRD. Relationships between time-varying PRAs and all-cause or cardiovascular mortality were assessed using Cox proportional hazards models. The analysis was repeated in subcohorts of candidates at lower risk for significant comorbidities, activated on the waiting list after 2007, or unsensitized at activation. Competing risks analyses were also conducted. Fully adjusted models showed increased hazard ratios (HRs [95% confidence intervals]) for all-cause mortality (HR, 1.02 [95% CI, 0.99 to 1.06]; HR, 1.11 [95% CI,1.07 to 1.16]; and HR,1.21 [95% CI,1.15 to 1.27]) and cardiovascular mortality (HR, 1.05 [95% CI,1.00 to 1.10]; HR,1.11 [95% CI,1.05 to 1.18]; and HR,1.21 [95% CI,1.12 to 1.31]) in PRA 1%-19%, PRA 20%-79%, and PRA 80%-100% categories compared with PRA 0%, respectively. Associations between PRA and the study outcomes were accentuated in competing risks models and in lower-risk patients and persisted in other subcohorts. Our findings suggest that PRA is an independent predictor of mortality in wait-listed kidney transplant candidates. The mechanisms by which PRA confers an incremental mortality risk in sensitized patients, and the role of transplantation in modifying this risk, warrant further study. |
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Whereas innate and adaptive immunity have established roles in cardiovascular disease, the role of humoral immunity is unknown. We conducted a retrospective cohort study in first-time adult kidney transplant candidates (N=161,308) using data from the Scientific Registry of Transplant Recipients and the Centers for Medicare and Medicaid Services to evaluate whether anti-human leukocyte antigen antibodies, measured as panel reactive antibodies (PRAs), are related to mortality in ESRD. Relationships between time-varying PRAs and all-cause or cardiovascular mortality were assessed using Cox proportional hazards models. The analysis was repeated in subcohorts of candidates at lower risk for significant comorbidities, activated on the waiting list after 2007, or unsensitized at activation. Competing risks analyses were also conducted. Fully adjusted models showed increased hazard ratios (HRs [95% confidence intervals]) for all-cause mortality (HR, 1.02 [95% CI, 0.99 to 1.06]; HR, 1.11 [95% CI,1.07 to 1.16]; and HR,1.21 [95% CI,1.15 to 1.27]) and cardiovascular mortality (HR, 1.05 [95% CI,1.00 to 1.10]; HR,1.11 [95% CI,1.05 to 1.18]; and HR,1.21 [95% CI,1.12 to 1.31]) in PRA 1%-19%, PRA 20%-79%, and PRA 80%-100% categories compared with PRA 0%, respectively. Associations between PRA and the study outcomes were accentuated in competing risks models and in lower-risk patients and persisted in other subcohorts. Our findings suggest that PRA is an independent predictor of mortality in wait-listed kidney transplant candidates. The mechanisms by which PRA confers an incremental mortality risk in sensitized patients, and the role of transplantation in modifying this risk, warrant further study.</description><identifier>ISSN: 1046-6673</identifier><identifier>EISSN: 1533-3450</identifier><identifier>DOI: 10.1681/ASN.2014090894</identifier><identifier>PMID: 26054537</identifier><language>eng</language><publisher>United States: American Society of Nephrology</publisher><subject>Cardiovascular Diseases - etiology ; Cardiovascular Diseases - mortality ; Clinical Epidemiology ; Cohort Studies ; Female ; HLA Antigens - blood ; Humans ; Kidney Failure, Chronic - blood ; Kidney Failure, Chronic - complications ; Kidney Failure, Chronic - immunology ; Kidney Failure, Chronic - mortality ; Kidney Failure, Chronic - surgery ; Kidney Transplantation ; Male ; Middle Aged ; Predictive Value of Tests ; Retrospective Studies ; Waiting Lists</subject><ispartof>Journal of the American Society of Nephrology, 2016-02, Vol.27 (2), p.570-578</ispartof><rights>Copyright © 2016 by the American Society of Nephrology.</rights><rights>Copyright © 2016 by the American Society of Nephrology 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-583f3d9ee9b594819e987f82ef8b284cc88269e6effab0cf53f860eb0ac4befa3</citedby><cites>FETCH-LOGICAL-c390t-583f3d9ee9b594819e987f82ef8b284cc88269e6effab0cf53f860eb0ac4befa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731107/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731107/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26054537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sapir-Pichhadze, Ruth</creatorcontrib><creatorcontrib>Tinckam, Kathryn J</creatorcontrib><creatorcontrib>Laupacis, Andreas</creatorcontrib><creatorcontrib>Logan, Alexander G</creatorcontrib><creatorcontrib>Beyene, Joseph</creatorcontrib><creatorcontrib>Kim, S Joseph</creatorcontrib><title>Immune Sensitization and Mortality in Wait-Listed Kidney Transplant Candidates</title><title>Journal of the American Society of Nephrology</title><addtitle>J Am Soc Nephrol</addtitle><description>Cardiovascular mortality is the leading cause of death in ESRD. Whereas innate and adaptive immunity have established roles in cardiovascular disease, the role of humoral immunity is unknown. We conducted a retrospective cohort study in first-time adult kidney transplant candidates (N=161,308) using data from the Scientific Registry of Transplant Recipients and the Centers for Medicare and Medicaid Services to evaluate whether anti-human leukocyte antigen antibodies, measured as panel reactive antibodies (PRAs), are related to mortality in ESRD. Relationships between time-varying PRAs and all-cause or cardiovascular mortality were assessed using Cox proportional hazards models. The analysis was repeated in subcohorts of candidates at lower risk for significant comorbidities, activated on the waiting list after 2007, or unsensitized at activation. Competing risks analyses were also conducted. Fully adjusted models showed increased hazard ratios (HRs [95% confidence intervals]) for all-cause mortality (HR, 1.02 [95% CI, 0.99 to 1.06]; HR, 1.11 [95% CI,1.07 to 1.16]; and HR,1.21 [95% CI,1.15 to 1.27]) and cardiovascular mortality (HR, 1.05 [95% CI,1.00 to 1.10]; HR,1.11 [95% CI,1.05 to 1.18]; and HR,1.21 [95% CI,1.12 to 1.31]) in PRA 1%-19%, PRA 20%-79%, and PRA 80%-100% categories compared with PRA 0%, respectively. Associations between PRA and the study outcomes were accentuated in competing risks models and in lower-risk patients and persisted in other subcohorts. Our findings suggest that PRA is an independent predictor of mortality in wait-listed kidney transplant candidates. The mechanisms by which PRA confers an incremental mortality risk in sensitized patients, and the role of transplantation in modifying this risk, warrant further study.</description><subject>Cardiovascular Diseases - etiology</subject><subject>Cardiovascular Diseases - mortality</subject><subject>Clinical Epidemiology</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>HLA Antigens - blood</subject><subject>Humans</subject><subject>Kidney Failure, Chronic - blood</subject><subject>Kidney Failure, Chronic - complications</subject><subject>Kidney Failure, Chronic - immunology</subject><subject>Kidney Failure, Chronic - mortality</subject><subject>Kidney Failure, Chronic - surgery</subject><subject>Kidney Transplantation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Predictive Value of Tests</subject><subject>Retrospective Studies</subject><subject>Waiting Lists</subject><issn>1046-6673</issn><issn>1533-3450</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkbtPwzAQxi0EouWxMqKMLCl27Dj2glRVPCpKGVrEaDnJGYwSp8QOUvnrCWopMN1J97vvHh9CZwSPCBfkcryYjxJMGJZYSLaHhiSlNKYsxft9jhmPOc_oAB15_4YxSZMsO0SDhOOUpTQbovm0rjsH0QKct8F-6mAbF2lXRg9NG3RlwzqyLnrWNsQz6wOU0b0tHayjZaudX1XahWjS87bUAfwJOjC68nC6jcfo6eZ6ObmLZ4-308l4FhdU4hCnghpaSgCZp5IJIkGKzIgEjMgTwYpCiIRL4GCMznFhUmoEx5BjXbAcjKbH6Gqju-ryGsoCXGh1pVatrXW7Vo226n_F2Vf10nwollFCcNYLXGwF2ua9Ax9UbX0BVX8PNJ1XJOOEcUkF7dHRBi3axvsWzG4MwerbBNWboH5N6BvO_y63w3--Tr8AT5SEkg</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Sapir-Pichhadze, Ruth</creator><creator>Tinckam, Kathryn J</creator><creator>Laupacis, Andreas</creator><creator>Logan, Alexander G</creator><creator>Beyene, Joseph</creator><creator>Kim, S Joseph</creator><general>American Society of Nephrology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160201</creationdate><title>Immune Sensitization and Mortality in Wait-Listed Kidney Transplant Candidates</title><author>Sapir-Pichhadze, Ruth ; Tinckam, Kathryn J ; Laupacis, Andreas ; Logan, Alexander G ; Beyene, Joseph ; Kim, S Joseph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-583f3d9ee9b594819e987f82ef8b284cc88269e6effab0cf53f860eb0ac4befa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cardiovascular Diseases - etiology</topic><topic>Cardiovascular Diseases - mortality</topic><topic>Clinical Epidemiology</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>HLA Antigens - blood</topic><topic>Humans</topic><topic>Kidney Failure, Chronic - blood</topic><topic>Kidney Failure, Chronic - complications</topic><topic>Kidney Failure, Chronic - immunology</topic><topic>Kidney Failure, Chronic - mortality</topic><topic>Kidney Failure, Chronic - surgery</topic><topic>Kidney Transplantation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Predictive Value of Tests</topic><topic>Retrospective Studies</topic><topic>Waiting Lists</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sapir-Pichhadze, Ruth</creatorcontrib><creatorcontrib>Tinckam, Kathryn J</creatorcontrib><creatorcontrib>Laupacis, Andreas</creatorcontrib><creatorcontrib>Logan, Alexander G</creatorcontrib><creatorcontrib>Beyene, Joseph</creatorcontrib><creatorcontrib>Kim, S Joseph</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Society of Nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sapir-Pichhadze, Ruth</au><au>Tinckam, Kathryn J</au><au>Laupacis, Andreas</au><au>Logan, Alexander G</au><au>Beyene, Joseph</au><au>Kim, S Joseph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune Sensitization and Mortality in Wait-Listed Kidney Transplant Candidates</atitle><jtitle>Journal of the American Society of Nephrology</jtitle><addtitle>J Am Soc Nephrol</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>27</volume><issue>2</issue><spage>570</spage><epage>578</epage><pages>570-578</pages><issn>1046-6673</issn><eissn>1533-3450</eissn><abstract>Cardiovascular mortality is the leading cause of death in ESRD. Whereas innate and adaptive immunity have established roles in cardiovascular disease, the role of humoral immunity is unknown. We conducted a retrospective cohort study in first-time adult kidney transplant candidates (N=161,308) using data from the Scientific Registry of Transplant Recipients and the Centers for Medicare and Medicaid Services to evaluate whether anti-human leukocyte antigen antibodies, measured as panel reactive antibodies (PRAs), are related to mortality in ESRD. Relationships between time-varying PRAs and all-cause or cardiovascular mortality were assessed using Cox proportional hazards models. The analysis was repeated in subcohorts of candidates at lower risk for significant comorbidities, activated on the waiting list after 2007, or unsensitized at activation. Competing risks analyses were also conducted. Fully adjusted models showed increased hazard ratios (HRs [95% confidence intervals]) for all-cause mortality (HR, 1.02 [95% CI, 0.99 to 1.06]; HR, 1.11 [95% CI,1.07 to 1.16]; and HR,1.21 [95% CI,1.15 to 1.27]) and cardiovascular mortality (HR, 1.05 [95% CI,1.00 to 1.10]; HR,1.11 [95% CI,1.05 to 1.18]; and HR,1.21 [95% CI,1.12 to 1.31]) in PRA 1%-19%, PRA 20%-79%, and PRA 80%-100% categories compared with PRA 0%, respectively. Associations between PRA and the study outcomes were accentuated in competing risks models and in lower-risk patients and persisted in other subcohorts. Our findings suggest that PRA is an independent predictor of mortality in wait-listed kidney transplant candidates. The mechanisms by which PRA confers an incremental mortality risk in sensitized patients, and the role of transplantation in modifying this risk, warrant further study.</abstract><cop>United States</cop><pub>American Society of Nephrology</pub><pmid>26054537</pmid><doi>10.1681/ASN.2014090894</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cardiovascular Diseases - etiology Cardiovascular Diseases - mortality Clinical Epidemiology Cohort Studies Female HLA Antigens - blood Humans Kidney Failure, Chronic - blood Kidney Failure, Chronic - complications Kidney Failure, Chronic - immunology Kidney Failure, Chronic - mortality Kidney Failure, Chronic - surgery Kidney Transplantation Male Middle Aged Predictive Value of Tests Retrospective Studies Waiting Lists |
title | Immune Sensitization and Mortality in Wait-Listed Kidney Transplant Candidates |
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