Study: Spinal cord injury causes acute and systemic muscle wasting

Acute spinal cord injury (SCI) patients lose body weight and muscle mass, despite being on a high-calorie diet while in the intensive care unit. Their muscle wasting is substantial and extends beyond what can explained by inactivity or denervation (loss of nerve supply) alone.

Research led by The Ohio State University Wexner Medical Center and College of Medicine published in the journal Science Translational Medicine sheds new light and decodes early muscle loss after SCI to provide an unprecedent first understanding that muscle wasting.

Researchers found that the severity of this SCI-induced systemic muscle wasting depends on location of the spinal cord injury (lesion level). More precisely, it depends on whether the adrenal gland becomes denervated after high thoracic injury (above T5), or not (after low thoracic injury).

They also found that systemic muscle loss is worsened when the adrenal glands become deprived of central nervous system control resulting in a skewed hormonal (endocrine) tone. When this happens, hypercortisolism (excess cortisol release) often develops after the spinal cord injury.

“This hypercortisolism then acts on specific receptors in the muscle of the entire body to cause muscle loss. Interfering with this pathway could rescue muscle tissue and improve the response to rehabilitation,” said first author Markus Harrigan, a member of Schwab’s research lab and Ohio State’s dual-degree MD-PhD Medical Scientist Training Program as well as a Ruth L. Kirschstein Individual NIH-Research Fellow.

This research also provides new insights on how to maintain muscle integrity while reducing the risk to develop higher degree pressure ulcers that often plague these patients, Harrigan said. The study builds on previous Ohio State research into the effects of SCI on the immune system that undermine immune system function, enhance infection susceptibility and contribute to infectious complications.

Reference: Study: Spinal cord injury causes acute and systemic muscle wasting; Science Translational Medicine, DOI: 10.1126/scitranslmed.adh2156