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- Publisher Website: 10.1373/clinchem.2006.078378
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- PMID: 17395709
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Article: Prognostic value of cardiac troponin T is independent of inflammation, residual renal function, and cardiac hypertrophy and dysfunction in peritoneal dialysis patients
Title | Prognostic value of cardiac troponin T is independent of inflammation, residual renal function, and cardiac hypertrophy and dysfunction in peritoneal dialysis patients |
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Authors | |
Issue Date | 2007 |
Publisher | American Association for Clinical Chemistry, Inc. The Journal's web site is located at http://www.clinchem.org |
Citation | Clinical Chemistry, 2007, v. 53 n. 5, p. 882-889 How to Cite? |
Abstract | Background: We investigated whether cardiac troponin T (cTnT) independently predicted outcome and added prognostic value over other clinical risk predictors in chronic peritoneal dialysis (PD) with end-stage renal disease. Methods: Baseline cTnT, echocardiography, indices of dialysis adequacy, and biochemical characteristics were assessed in 238 chronic PD patients who were followed prospectively for 3 years or until death. Results: Using multivariable Cox regression analysis, cTnT remained predictive of all-cause mortality [hazard ratio 4.43, 95% CI 1.87-10.45, P = 0.001], cardiovascular death (4.12, 1.29-13.17, P = 0.017), noncardiovascular death (8.06, 1.86-35.03, P = 0.005), and fatal and nonfatal cardiovascular events (CVEs) (3.59,1.48-8.70, P = 0.005) independent of background coronary artery disease, inflammation, residual renal function, left ventricular hypertrophy, and systolic dysfunction. cTnT alone had better predictive value than C-reactive protein (CRP) alone for mortality [area under the ROC curve (AUC) 0.774 vs 0.691; P = 0.089] and first CVE (AUC 0.711 vs 0.593; P = 0.009) at 3 years. Survival models including age, sex, and clinical, biochemical, and echocardiography characteristics yielded AUCs of 0.813 (95% CI, 0.748-0.877), 0.800 (95% CI, 0.726-0.874), and 0.769 (95% CI, 0.708-0.830), respectively, in relation to all-cause mortality, cardiovascular death, and fatal and nonfatal cardiovascular events. After addition of cTnT, AUCs of the above models increased significantly to 0.832 (95% CI, 0.669-0.894; P = 0.0037), 0.810 (95% CI, 0.739-0.883; P = 0.0036), and 0.780 (95% CI, 0.720-0.840; P = 0.0002), respectively; no AUCs increased when CRP was added. Conclusions: cTnT is an independent predictor of longterm mortality, cardiovascular death and events, and noncardiovascular death in PD patients. © 2007 American Association for Clinical Chemistry. |
Persistent Identifier | http://hdl.handle.net/10722/163079 |
ISSN | 2023 Impact Factor: 7.1 2023 SCImago Journal Rankings: 1.460 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wang, AYM | en_US |
dc.contributor.author | Lam, CWK | en_US |
dc.contributor.author | Wang, M | en_US |
dc.contributor.author | Chan, IHS | en_US |
dc.contributor.author | Goggins, WB | en_US |
dc.contributor.author | Yu, CM | en_US |
dc.contributor.author | Lui, SF | en_US |
dc.contributor.author | Sanderson, JE | en_US |
dc.date.accessioned | 2012-09-05T05:27:19Z | - |
dc.date.available | 2012-09-05T05:27:19Z | - |
dc.date.issued | 2007 | en_US |
dc.identifier.citation | Clinical Chemistry, 2007, v. 53 n. 5, p. 882-889 | en_US |
dc.identifier.issn | 0009-9147 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/163079 | - |
dc.description.abstract | Background: We investigated whether cardiac troponin T (cTnT) independently predicted outcome and added prognostic value over other clinical risk predictors in chronic peritoneal dialysis (PD) with end-stage renal disease. Methods: Baseline cTnT, echocardiography, indices of dialysis adequacy, and biochemical characteristics were assessed in 238 chronic PD patients who were followed prospectively for 3 years or until death. Results: Using multivariable Cox regression analysis, cTnT remained predictive of all-cause mortality [hazard ratio 4.43, 95% CI 1.87-10.45, P = 0.001], cardiovascular death (4.12, 1.29-13.17, P = 0.017), noncardiovascular death (8.06, 1.86-35.03, P = 0.005), and fatal and nonfatal cardiovascular events (CVEs) (3.59,1.48-8.70, P = 0.005) independent of background coronary artery disease, inflammation, residual renal function, left ventricular hypertrophy, and systolic dysfunction. cTnT alone had better predictive value than C-reactive protein (CRP) alone for mortality [area under the ROC curve (AUC) 0.774 vs 0.691; P = 0.089] and first CVE (AUC 0.711 vs 0.593; P = 0.009) at 3 years. Survival models including age, sex, and clinical, biochemical, and echocardiography characteristics yielded AUCs of 0.813 (95% CI, 0.748-0.877), 0.800 (95% CI, 0.726-0.874), and 0.769 (95% CI, 0.708-0.830), respectively, in relation to all-cause mortality, cardiovascular death, and fatal and nonfatal cardiovascular events. After addition of cTnT, AUCs of the above models increased significantly to 0.832 (95% CI, 0.669-0.894; P = 0.0037), 0.810 (95% CI, 0.739-0.883; P = 0.0036), and 0.780 (95% CI, 0.720-0.840; P = 0.0002), respectively; no AUCs increased when CRP was added. Conclusions: cTnT is an independent predictor of longterm mortality, cardiovascular death and events, and noncardiovascular death in PD patients. © 2007 American Association for Clinical Chemistry. | en_US |
dc.language | eng | en_US |
dc.publisher | American Association for Clinical Chemistry, Inc. The Journal's web site is located at http://www.clinchem.org | en_US |
dc.relation.ispartof | Clinical Chemistry | en_US |
dc.subject.mesh | Biological Markers - Analysis | en_US |
dc.subject.mesh | C-Reactive Protein - Analysis | en_US |
dc.subject.mesh | Cardiomegaly - Diagnosis - Mortality - Physiopathology | en_US |
dc.subject.mesh | Cardiovascular Diseases - Diagnosis - Mortality - Physiopathology | en_US |
dc.subject.mesh | Echocardiography | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Inflammation - Diagnosis | en_US |
dc.subject.mesh | Kidney Failure, Chronic - Diagnosis - Mortality - Therapy | en_US |
dc.subject.mesh | Kidney Function Tests | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Peritoneal Dialysis | en_US |
dc.subject.mesh | Predictive Value Of Tests | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Prospective Studies | en_US |
dc.subject.mesh | Risk | en_US |
dc.subject.mesh | Survival Rate | en_US |
dc.subject.mesh | Troponin T - Blood | en_US |
dc.title | Prognostic value of cardiac troponin T is independent of inflammation, residual renal function, and cardiac hypertrophy and dysfunction in peritoneal dialysis patients | en_US |
dc.type | Article | en_US |
dc.identifier.email | Wang, M:meiwang@hkucc.hku.hk | en_US |
dc.identifier.authority | Wang, M=rp00281 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1373/clinchem.2006.078378 | en_US |
dc.identifier.pmid | 17395709 | - |
dc.identifier.scopus | eid_2-s2.0-34248339058 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34248339058&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 53 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.spage | 882 | en_US |
dc.identifier.epage | 889 | en_US |
dc.identifier.isi | WOS:000246248100012 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Wang, AYM=13606226000 | en_US |
dc.identifier.scopusauthorid | Lam, CWK=8531362100 | en_US |
dc.identifier.scopusauthorid | Wang, M=7406690398 | en_US |
dc.identifier.scopusauthorid | Chan, IHS=8298775100 | en_US |
dc.identifier.scopusauthorid | Goggins, WB=6701315434 | en_US |
dc.identifier.scopusauthorid | Yu, CM=7404976646 | en_US |
dc.identifier.scopusauthorid | Lui, SF=7102379144 | en_US |
dc.identifier.scopusauthorid | Sanderson, JE=7202371250 | en_US |
dc.identifier.citeulike | 7634157 | - |
dc.identifier.issnl | 0009-9147 | - |