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Prognostic value of free triiodothyronine in patients with dilated cardiomyopathy
Hong-Yan Zhao1, Ling Sun2, Ye-Qian Zhu1
1Section of Pacing and Electrophysiology, Division of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.
Insights
Low free triiodothyronine (FT3) levels are linked to a higher risk of death in patients with dilated cardiomyopathy (DCM). This study highlights FT3 as a potential prognostic marker for DCM patients.
Area of Science:
- Cardiology
- Endocrinology
- Biochemistry
Background:
- Dilated cardiomyopathy (DCM) prognosis is not fully understood.
- The role of free triiodothyronine (FT3) in DCM long-term outcomes remains unevaluated.
Purpose of the Study:
- To investigate the prognostic value of FT3 levels in patients diagnosed with DCM.
- To determine if FT3 can predict long-term mortality in DCM patients.
Main Methods:
- Collected data from 146 DCM patients (October 2009 - December 2014).
- Measured FT3 levels and other biochemical markers.
- Utilized Pearson analysis and Cox hazards model for prognosis assessment over a median follow-up of 79.9 months.
Main Results:
- Lower FT3 levels were observed in non-survivors compared to survivors (P=0.003).
- FT3 correlated positively with red blood cell and hemoglobin, and negatively with age, BUN, and creatinine.
- Patients with FT3 ≤3.49 pmol/L had a significantly higher risk of all-cause mortality (P=0.001).
- Multivariate analysis confirmed FT3's significant association with all-cause mortality (HR: 0.70, P=0.021).
Conclusions:
- Reduced FT3 levels are associated with increased all-cause mortality in DCM patients.
- FT3 may serve as a valuable prognostic biomarker for DCM.
Background:
The association between free triiodothyronine (FT3) and long-term prognosis in dilated cardiomyopathy (DCM) patients has not been evaluated. The purpose of this study was to determine whether the level of FT3 could provide prognostic value in patients with DCM.
Methods:
Data of consecutive patients diagnosed with DCM were collected from October 2009 to December 2014. FT3 was measured by fluoroimmunoassay. Other biochemical markers, such as free thyroxin (FT4), thyroid-stimulating hormone, red blood cell, hemoglobin, blood urea nitrogen, and serum creatinine, were tested at the same time. Follow-up was performed every 3 months. The primary endpoint was all-cause mortality. Pearson analysis was used to evaluate the correlation of FT3 and other lab metrics with DCM patients' prognosis. The association of long-term mortality in DCM and FT3 was compared using Cox hazards model.
Results:
Data of 176 patients diagnosed with DCM were collected. Of them, 24 patients missed FT3 values and six patients were lost to follow-up. Altogether, data of 146 patients were analyzed. During the median follow-up time of 79.9 (53.5-159.6) months, nine patients lost, 61 patients died (non-survival group), and 85 patients survived (survival group). FT3 was significantly lower in non-survival group than that in survival group (3.65 ± 0.83 pmol/L vs. 4.36 ± 1.91 pmol/L; P = 0.003). FT3 also showed a significantly positive correlation with red blood cell and hemoglobin, negatively correlated with age, blood urea nitrogen and serum creatinine (P < 0.05), respectively. Patients in the group of lower FT3 levels (FT3 ≤3.49 pmol/L) suffered from a higher risk of all-cause mortality (P for log-rank = 0.001). In multivariate Cox regression analysis, FT3 level was significantly associated with all-cause mortality (hazard ratio: 0.70, 95% confidence interval 0.52-0.95, P for trend = 0.021).
Conclusion:
Low levels of FT3 were associated with increased all-cause mortality in patients with DCM.
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