Gould Paul A, Kong Grace, Kalff Victor, Duffy Stephen J, Taylor Andrew J, Kelly Michael J, Kaye David M
Wynn Department of Metabolic Cardiology, Baker Heart Research Institute, Central, Melbourne VIC, Australia.
Europace. 2007 Sep;9(9):751-6. doi: 10.1093/europace/eum081. Epub 2007 May 21.
We investigated whether biventricular (BiV) pacing favourably affects cardiac sympathetic activity in heart failure (HF).
In 10 HF patients treated with BiV pacing, we assessed cardiac sympathetic activity by metaiodobenzylguanidine ((123)I-MIBG) imaging. Patients were randomized in a double-blinded crossover fashion, for two weeks of either inactivation of BiV pacing or BiV pacing, with crossover to the alternate group for a further two weeks. After randomization blocks, cardiac (123)I-MIBG imaging and a 6 min walk test were performed. BiV pacing was associated with significant improvements in cardiac (123)I-MIBG uptake reflected by increases in early (BiV 1.71 +/- 0.09 vs. non-BiV 1.63 +/- 0.06, P = 0.03) and late (at 4 h) heart to mediastinal ratio of uptake (BiV 1.54 +/- 0.08 vs. non-BiV 1.45 +/- 0.06, P = 0.03). Additionally, pulmonary (123)I-MIBG uptake, measured as lung to mediastinal ratio, significantly improved (P = 0.009). Six-minute walk and systolic blood pressure tended to improve with BiV vs. non-BiV pacing (P = 0.09).
In patients with stable HF, BiV pacing is associated with long-term improvements in cardiac sympathetic nerve activity, as reflected by improvements in cardiac (123)I-MIBG uptake. This is a potential mechanism for morbidity and mortality benefits observed in larger studies.
我们研究了双心室(BiV)起搏是否对心力衰竭(HF)患者的心脏交感神经活动产生有利影响。
在10例接受BiV起搏治疗的HF患者中,我们通过间碘苄胍((123)I-MIBG)显像评估心脏交感神经活动。患者以双盲交叉方式随机分组,进行为期两周的BiV起搏失活或BiV起搏,然后交叉至另一组再进行两周。在随机分组后,进行心脏(123)I-MIBG显像和6分钟步行试验。BiV起搏与心脏(123)I-MIBG摄取的显著改善相关,表现为早期(BiV组1.71±0.09 vs.非BiV组1.63±0.06,P = 0.03)和晚期(4小时)心脏与纵隔摄取比值增加(BiV组1.54±0.08 vs.非BiV组1.45±0.06,P = 0.03)。此外,以肺与纵隔比值测量的肺部(123)I-MIBG摄取也显著改善(P = 0.009)。与非BiV起搏相比,BiV起搏时6分钟步行距离和收缩压有改善趋势(P = 0.09)。
在稳定HF患者中,BiV起搏与心脏交感神经活动长期改善相关,表现为心脏(123)I-MIBG摄取增加。这是在更大规模研究中观察到发病率和死亡率获益的潜在机制。