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Prognostic value of plasma big endothelin-1 in patients with light chain cardiac amyloidosis
Zhongli Chen1, Anteng Shi1, Zhiyan Wang2
1State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Insights
High big endothelin-1 (ET-1) levels predict mortality in light chain cardiac amyloidosis (AL-CA). This biomarker may aid risk stratification for patients with moderate to severe AL-CA.
Area of Science:
- Cardiology
- Biomarkers
- Amyloidosis Research
Background:
- Light chain cardiac amyloidosis (AL-CA) has a high mortality rate.
- Big endothelin-1 (ET-1) is linked to bioactive ET-1 levels.
- The prognostic significance of big ET-1 in AL-CA was previously undocumented.
Purpose of the Study:
- To assess the prognostic value of big endothelin-1 (ET-1) for adverse outcomes in moderate to severe AL-CA.
- To investigate big ET-1 as a predictor of mortality in AL-CA patients.
Main Methods:
- Retrospective study of 141 patients with newly diagnosed AL-CA (modified Mayo 2004 stage II or III).
- Big ET-1 levels measured on admission.
- Primary outcome: all-cause mortality; secondary outcomes: cardiac death and heart failure hospitalizations.
Main Results:
- Higher big ET-1 levels (>0.88 pmol/L) were associated with significantly shorter survival (15.3 months vs. 34.1 months).
- Big ET-1 was an independent predictor of all-cause mortality (HR 1.91, p=0.035).
- Big ET-1 improved prognostic accuracy beyond the modified Mayo 2004 stage (C-index increase, p=0.025).
Conclusions:
- Big endothelin-1 is a potent and independent predictor of mortality in moderate to severe AL-CA.
- Big ET-1 may play a role in risk stratification for AL-CA patients.
Background:
Light chain cardiac amyloidosis (AL-CA) is associated with a high incidence of mortality. Big endothelin-1 (ET-1), the precursor of endothelial-vasoconstrictive ET-1, is closely related to the concentration of bioactive ET-1. Association between big ET-1 and prognosis of AL-CA has not yet been documented. The purpose of this study was to evaluate the prognostic value of big ET-1 for poor outcomes in moderate to severe AL-CA.
Methods:
Big ET-1 levels were determined on admission in patients with newly diagnosed AL-CA with modified Mayo 2004 stage II or III. Primary outcome was all-cause mortality. The secondary outcomes included death from cardiac cause and the composite of the primary outcome or hospitalisations due to worsening heart failure.
Results:
Overall, 141 patients were retrospectively included (57 stage II, 34 stage IIIa, 50 stage IIIb). During a median follow-up time of 25.7 months, 84 (59.6%) patients died. Patients with big ET-1 levels of ≤0.88 pmol/L had longer survival than those with >0.88 pmol/L (median survival time: 34.1 months vs 15.3 months, log-rank p<0.001), which was also observed in the validation cohort (log-rank p=0.026). Higher big ET-1 levels were predictive for all-cause mortality after multivariable adjustment (HR 1.91, 95% CI 1.05 to 3.49, p=0.035). Big ET-1 levels added an incremental prognostic value over modified Mayo 2004 stage (C-index: from 0.671 to 0.696, p=0.025; integrated discrimination improvement 0.168, p=0.047).
Conclusions:
Big ET-1 is a strong and independent predictor of mortality in patients with moderate to severe AL-CA, which may indicate a possible role for risk stratification in patients with this disease.
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