Key result
Respiratory pathology is linked to ~30% more nerve cell bodies in the left stellate ganglion.
Observational (n=32)
No
Absolute Event Rate: 33.3% vs 25.7%
p-value: p=0.023
Sympathetic hyperinnervation due to nerve sprouting generated by the left stellate ganglion has been noted following cardiopulmonary disease processes. Sympathetic hyperinnervation seems to be limited to cardiopulmonary diseases in the experimental and clinical settings. However, histological changes of the left stellate ganglion following cardiopulmonary diseases in humans have vet to be observed. This study intends to investigate the histological changes of cadaveric sympathetic nervous tissue of left stellate ganglia (n = 32) and their relationship to noted pathology. Our study found fibrotic changes of the left stellate ganglion are not significantly dependent upon pathological processes, however, changes in the number of nerve cell bodies seems to be pathology dependent. A relationship between respiratory (mean = 33.3; P = 0.023) and cardiovascular pathologies (mean = 29.6; P = 0.199) and an increase in nerve cell bodies of the left stellate ganglion was noted when compared to other pathologies (mean = 25.7). The link between cardiopulmonary disease and sympathetic hyperinnervation may be the increase in the number of nerve cell bodies of the left stellate ganglion. Our results are clinically significant considering sympathetic hyperinnervation is associated with arrythmogenesis and an increase in morbidity and mortality in patients with pulmonary disease. Such findings may warrant investigation into the use of ganglion blockade in cardiopulmonary diseases.
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Docimo et al. (2008) conducted an observational in Cardiopulmonary disease (n=32). Respiratory disease pathology vs. Other pathological processes excluding the cardiopulmonary system was evaluated on Mean nerve cell bodies per high-powered field (p=0.023). Respiratory disease pathology was associated with a statistically significant increase in the mean number of nerve cell bodies in the left stellate ganglion compared to non-cardiopulmonary pathologies.
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