Key result
Unused donor hearts with dysfunction are linked to ~1.6-fold higher myocardial TNF-α expression versus used hearts.
Why the study?
Myocardial dysfunction is common in donor hearts, but the mechanisms responsible remain unclear.
Observational (n=82)
Elevated expression of inflammatory cytokines TNF-α and IL-6 in the myocardium and serum is associated with myocardial dysfunction in donor hearts, suggesting a potential mechanism and therapeutic target.
Answers are grounded in this paper and cite their sources.
Elevated cytokines should not yet alter donor acceptance; hypothesis-generating for anti-inflammatory strategies to expand the donor pool.
Background —Myocardial dysfunction is a common and important problem in donor hearts. The mechanisms responsible remain unclear. We have studied the cytokines tumor necrosis factor (TNF)-α and interleukin-6 (IL-6) in the myocardium and serum from donors with myocardial dysfunction (unused donors) and compared them with donors with good ventricular function (used donors) and patients with advanced heart failure (HF). Methods and Results —Clinical details and ventricular function were assessed in 46 donors (31 used, 15 unused). Real-time reverse transcription–polymerase chain reaction, Western blotting, and immunocytochemistry were performed on myocardium and immunoassays on serum. TNF-α mRNA was 1.6-fold higher in unused than in used donors ( P <0.005) and 1.74-fold higher than in 36 patients with HF. IL-6 mRNA was 2.4-fold higher in unused than in used donors ( P <0.0001) and 4.67-fold higher than in HF ( P <0.0001). Western blotting showed higher TNF-α in unused (218.3±6.4, n=4 versus 187.3±5.4, n=3 OD units) than used donors ( P <0.05). TNF-α expression was localized to cardiac myocytes. Serum TNF-α was higher in unused (8.72±1.3 pg/mL, n=13) than in used (6.12±0.8 pg/mL, n=25, P <0.05) donors and HF (4.0±0.4 pg/mL, n=17, P <0.005). Serum TNF-α receptors did not differ between unused (4.3±0.8 and 8.6±1.6 ng/mL, n=10) and used (3.5±0.4 and 6.5±1.1 ng/mL, n=24) donors. There was a trend for higher serum IL-6 in unused (16.5±2.9 pg/mL, n=9) compared with used (13.9±1.6 pg/mL, n=26, P =NS) donors. Conclusions —This study documented an increase in the expression of TNF-α and IL-6 in the myocardium of all donor hearts that was more marked in the dysfunctional (unused) donor hearts. This was accompanied by similar changes in the serum. This might have important therapeutic implications.
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Birks et al. (2000) conducted an observational in Myocardial dysfunction in donor hearts (n=82). Myocardial dysfunction (unused donor status) vs. Used donor hearts and advanced heart failure was evaluated on Myocardial TNF-α mRNA expression (1.6-fold higher, p=<0.005). Unused donor hearts with myocardial dysfunction had significantly higher myocardial TNF-α (1.6-fold, P<0.005) and IL-6 (2.4-fold, P<0.0001) mRNA expression compared to used donor hearts.
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