J 2012

Prognostic Utility of Biomarkers in Predicting of One- Year Outcomes in Patients with Aortic Stenosis Treated with Transcatheter or Surgical Aortic Valve Implantation

PAŘENICA, Jiří; Petr NĚMEC; Josef TOMANDL; Jiří ONDRÁŠEK; Monika PÁVKOVÁ GOLDBERGOVÁ et al.

Základní údaje

Originální název

Prognostic Utility of Biomarkers in Predicting of One- Year Outcomes in Patients with Aortic Stenosis Treated with Transcatheter or Surgical Aortic Valve Implantation

Autoři

PAŘENICA, Jiří; Petr NĚMEC; Josef TOMANDL ORCID; Jiří ONDRÁŠEK; Monika PÁVKOVÁ GOLDBERGOVÁ; Martin TŘETINA; Jiří JARKOVSKÝ ORCID; Simona LITTNEROVÁ; Martin POLOCZEK; Petr POKORNÝ; Jindřich ŠPINAR; Zdeňka ČERMÁKOVÁ; Roman MIKLÍK; Petr MALÍK; Ondřej PEŠ; Jolana LIPKOVÁ ORCID; Marie TOMANDLOVÁ a Petr KALA

Vydání

PloS ONE, 2012, 1932-6203

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30201 Cardiac and Cardiovascular systems

Stát vydavatele

Česká republika

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 3.730

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14110/12:00062521

Organizační jednotka

Lékařská fakulta

Klíčová slova anglicky

Aortic Stenosis; Transcatheter; Aortic Valve Implantation; Outcome
Změněno: 22. 4. 2013 18:46, Ing. Mgr. Věra Pospíšilíková

Anotace

V originále

Objectives: The aim of the work was to find biomarkers identifying patients at high risk of adverse clinical outcomes after TAVI and SAVR in addition to currently used predictive model (EuroSCORE). Methods: The multi-biomarker sub-study included 42 consecutive high-risk patients (average age 82.0 years; logistic EuroSCORE 21.0%) allocated to TAVI transfemoral and transapical using the Edwards-Sapien valve (n = 29), or SAVR with the Edwards Perimount bioprosthesis (n = 13). Standardized endpoints were prospectively followed during the 12-month follow-up. Results: The clinical outcomes after both TAVI and SAVR were comparable. Malondialdehyde served as the best predictor of a combined endpoint at 1 year with AUC (ROC analysis) = 0.872 for TAVI group, resp. 0.765 (p,0.05) for both TAVI and SAVR groups. Increased levels of MDA, matrix metalloproteinase 2, tissue inhibitor of metalloproteinase (TIMP1), ferritin-reducing ability of plasma, homocysteine, cysteine and 8-hydroxy-2-deoxyguanosine were all predictors of the occurrence of combined safety endpoints at 30 days (AUC 0.750–0.948; p,0.05 for all). The addition of MDA to a currently used clinical model (EuroSCORE) significantly improved prediction of a combined safety endpoint at 30 days and a combined endpoint (0–365 days) by the net reclassification improvement (NRI) and the integrated discrimination improvement (IDI) (p,0.05). Cystatin C, glutathione, cysteinylglycine, asymmetric dimethylarginine, nitrite/nitrate and MMP9 did not prove to be significant. Total of 14.3% died during 1-year follow-up. Conclusion: We identified malondialdehyde, a marker of oxidative stress, as the most promising predictor of adverse outcomes during the 30-day and 1-year follow-up in high-risk patients with symptomatic, severe aortic stenosis treated with TAVI. The development of a clinical ‘‘TAVIscore’’ would be highly appreciated. Such dedicated scoring system would enable further testing of adjunctive value of various biomarkers.

Návaznosti

MUNI/A/0831/2011, interní kód MU
Název: Příspěvek chemických a biochemických metodik ke studiu molekulární podstaty vybraných patologických stavů a onemocnění
Investor: Masarykova univerzita, Příspěvek chemických a biochemických metodik ke studiu molekulární podstaty vybraných patologických stavů a onemocnění, DO R. 2020_Kategorie A - Specifický výzkum - Studentské výzkumné projekty