Key result
Immunoadsorption plus IgG replacement improves LVEF by ~8% versus controls in dilated cardiomyopathy.
Why the study?
Although IA/IG has shown potential in dilated cardiomyopathy, only small-scale clinical trials have been reported, and its efficacy and safety characteristics required systematic evaluation.
Does immunoadsorption and subsequent immunoglobulin G replacement (IA/IG) improve left ventricular ejection fraction in patients with dilated cardiomyopathy?
Meta-Analysis (n=809)
Does immunoadsorption and subsequent immunoglobulin G replacement (IA/IG) improve left ventricular ejection fraction in patients with dilated cardiomyopathy?
Mean Difference: 8.31 (95% CI 6.45–10.18)
p-value: p=<0.00001
IA/IG therapy added to standard medical treatment significantly improves left ventricular ejection fraction and functional capacity in patients with dilated cardiomyopathy.
Background Dilated cardiomyopathy (DCM) is a refractory cardiac disease with significant morbidity and mortality. Although immune adsorption combined with immunoglobulin G replacement therapy (IA/IG) has shown potential in treating DCM, only small-scale clinical trials have been reported. Its efficacy and safety characteristics still need to be further systematically evaluated. Methods We conducted a systematic review and meta-analysis in accordance with PRISMA 2020 guidelines. A comprehensive search of PubMed, Embase, Web of Science, and the Cochrane Library was performed up to July 1, 2025. Clinical studies on IA/IG treatment for DCM were included. The primary outcome was the left ventricular ejection fraction (LVEF) change. Secondary outcomes included left ventricular end-diastolic dimension (LVEDD), NYHA functional class, N-terminal pro-brain natriuretic peptide (NT-proBNP), and VO2 peak. Study quality and risk of bias were assessed using the Cochrane ROB 2.0 and ROBINS-I tools. Sensitivity analysis was taken into consideration to determine the stability of the results. This review was registered with PROSPERO (CRD420251104796). Results Eighteen studies (2 RCTs and 16 non-RCTs) involving 809 participants were included. IA/IG therapy significantly improved LVEF [mean difference (MD) = 7.71%, 95% CI: 6.18–9.24, p < 0.00001] and reduced LVEDD (MD = −3.22 mm, 95% CI: −4.16 to −2.28, p < 0.00001) from baseline. Significant improvements were also observed in NYHA functional class (MD = −0.76, 95% CI: −0.91 to −0.60, p < 0.00001) and peak VO₂ (MD = 2.66 mL/kg/min, 95% CI: 1.26–4.06, p = 0.0002). Compared to controls, the IA/IG group demonstrated greater improvement in LVEF (MD = 8.31%, 95% CI: 6.45–10.18, p < 0.00001) and NYHA class (MD = –0.62, 95% CI: −1.00 to −0.25, p = 0.001). A sensitivity analysis of the results suggested that they were stable. Conclusion Systematic reviews and meta-analyses suggest that IA/IG therapy may improve cardiac function and quality of life in patients with DCM. However, the number of RCTs included in the study is limited, so these results should be interpreted with caution. Further high-quality, large-scale trials are warranted to establish standardized treatment protocols and confirm the long-term benefits of IA/IG therapy. Systematic Review Registration https://www.crd.york.ac.uk/PROSPERO/recorddashboard , PROSPERO CRD420251104796.
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Xia et al. (2026) conducted a meta-analysis in Dilated cardiomyopathy (DCM) (n=809). Immunoadsorption and subsequent immunoglobulin G replacement (IA/IG) vs. Optimal medical treatments alone was evaluated on Left ventricular ejection fraction (LVEF) change (MD 8.31%, 95% CI 6.45-10.18, p=<0.00001). Immunoadsorption and subsequent immunoglobulin G replacement therapy significantly improved left ventricular ejection fraction by a mean difference of 8.31% compared to controls in patients with dilated cardiomyopathy.
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