Monitoring the Efficacy of Tafamidis in ATTR Cardiac Amyloidosis by MRI-ECV: A Systematic Review and Meta-Analysis
- PMID: 39195732
- PMCID: PMC11360159
- DOI: 10.3390/tomography10080097
Monitoring the Efficacy of Tafamidis in ATTR Cardiac Amyloidosis by MRI-ECV: A Systematic Review and Meta-Analysis
Abstract
Background: The usefulness of monitoring treatment effect of tafamidis using magnetic resonance imaging (MRI) extracellular volume fraction (ECV) has been reported.
Objective: we conducted a meta-analysis to evaluate the usefulness of this method.
Methods: Data from 246 ATTR-CMs from six studies were extracted and included in the analysis. An inverse variance meta-analysis using a random effects model was performed to evaluate the change in MRI-ECV before and after tafamidis treatment. The analysis was also performed by classifying the patients into ATTR-CM types (wild-type or hereditary).
Results: ECV change before and after tafamidis treatment was 0.33% (95% CI: -1.83-2.49, I2 = 0%, p = 0.76 for heterogeneity) in the treatment group and 4.23% (95% CI: 0.44-8.02, I2 = 0%, p = 0.18 for heterogeneity) in the non-treatment group. The change in ECV before and after treatment was not significant in the treated group (p = 0.76), but there was a significant increase in the non-treated group (p = 0.03). There was no difference in the change in ECV between wild-type (95% CI: -2.65-3.40) and hereditary-type (95% CI: -9.28-4.28) (p = 0.45).
Conclusions: The results of this meta-analysis suggest that MRI-ECV measurement is a useful imaging method for noninvasively evaluating the efficacy of tafamidis treatment for ATTR-CM.
Keywords: cardiac MRI; cardiac amyloidosis; extracellular volume fraction; meta-analysis; tafamidis.
Conflict of interest statement
The authors declare no conflict of interest.
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References
-
- Lane T., Fontana M., Martinez-Naharro A., Quarta C.C., Whelan C.J., Petrie A., Rowczenio D.M., Gilbertson J.A., Hutt D.F., Rezk T., et al. Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis. Circulation. 2019;140:16–26. doi: 10.1161/CIRCULATIONAHA.118.038169. - DOI - PubMed
-
- Gilstrap L.G., Dominici F., Wang Y., El-Sady M.S., Singh A., Di Carli M.F., Falk R.H., Dorbala S. Epidemiology of Cardiac Amyloidosis-Associated Heart Failure Hospitalizations Among Fee-for-Service Medicare Beneficiaries in the United States. Circ. Heart Fail. 2019;12:e005407. doi: 10.1161/CIRCHEARTFAILURE.118.005407. - DOI - PMC - PubMed
-
- Hahn V.S., Yanek L.R., Vaishnav J., Ying W., Vaidya D., Lee Y.Z.J., Riley S.J., Subramanya V., Brown E.E., Hopkins C.D., et al. Endomyocardial Biopsy Characterization of Heart Failure with Preserved Ejection Fraction and Prevalence of Cardiac Amyloidosis. JACC Heart Fail. 2020;8:712–724. doi: 10.1016/j.jchf.2020.04.007. - DOI - PMC - PubMed
-
- Castaño A., Narotsky D.L., Hamid N., Khalique O.K., Morgenstern R., DeLuca A., Rubin J., Chiuzan C., Nazif T., Vahl T., et al. Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement. Eur. Heart J. 2017;38:2879–2887. doi: 10.1093/eurheartj/ehx350. - DOI - PMC - PubMed
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