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October 07, 2013
Study Shows How Binge Drinking Impairs Healing of Broken Bones
MAYWOOD, Ill. – Physicians have long observed that binge drinking can significantly impair the healing process following a bone fracture.
Now a study by Loyola University Medical Center researchers is providing insights into how alcohol slows healing on the cellular and molecular levels. The findings could lead to treatments to improve bone healing in alcohol abusers, and possibly non-drinkers as well.
Roman Natoli, MD, PhD, presented these findings Sunday, Oct. 6, during the American Society for Bone and Mineral Research 2013 Annual Meeting in Baltimore. Senior author is John Callaci, PhD. The study was funded by the Orthopaedic Research and Education Foundation.
“Many bone fractures are alcohol-related, due to car accidents, falls, shootings, etc.,” Natoli said. “In addition to contributing to bone fractures, alcohol also impairs the healing process. So add this to the list of reasons why you should not abuse alcohol."
Researchers studied the effects that alcohol consumption had on bone healing in mice. One group of mice was exposed to alcohol levels roughly equivalent to three times the legal limit for driving. A control group was exposed to equal amounts of saline (salt water).
The study found three ways in which alcohol impaired bone healing after a fracture:
There were differences between the control group and the alcohol-exposed group in the callus, the hard bony tissue that forms around the ends of fractured bones. In the alcohol-exposed group, the callus was less mineralized, meaning not as much bone was forming. Moreover, the bone that did form was not as strong.
Mice exposed to alcohol showed signs of oxidative stress, a process that impairs normal cellular functions. The alcohol-exposed mice had significantly higher levels of malondialdehyde, a molecule that serves as a marker for oxidative stress. Additionally, levels of an enzyme that decreases oxidative stress, superoxide dismutase, were higher in the alcohol-exposed mice (but not quite high enough to be considered statistically significant).
During the healing process, the body sends immature stem cells to a fracture site. After arriving at the site, the stem cells mature into bone cells. Two proteins, known as SDF-1 and OPN, are involved in recruiting stem cells to the injury site. In the alcohol-exposed group, OPN levels were significantly lower.
As a follow-up to this study, Natoli is planning an animal-model study on two potential treatments to counter the negative effects of alcohol on bone healing. One treatment would be to inject mice with stem cells to improve healing. The other treatment would be the administration of NAc, an antioxidant that combats oxidative stress.
If such treatments were shown to be effective in alcohol abusers, it’s possible the treatments also might speed healing in non-drinkers as well, Natoli said.
Natoli is a resident physician in the Department of Orthopaedic Surgery and Rehabilitation at Loyola University Chicago Stritch School of Medicine. Callaci is an assistant professor in the Department of Orthopaedic Surgery and Rehabilitation. The third author is Rachel Mauer, BS, a research technician.
The Loyola University Chicago Health Sciences Division (HSD) advances interprofessional, multidisciplinary, and transformative education and research while promoting service to others through stewardship of scientific knowledge and preparation of tomorrow's leaders. The HSD is located on the Health Sciences Campus in Maywood, Illinois. It includes the Marcella Niehoff School of Nursing, the Stritch School of Medicine, the biomedical research programs of the Graduate School, and several other institutes and centers encouraging new research and interprofessional education opportunities across all of Loyola University Chicago. The faculty and staff of the HSD bring a wealth of knowledge, experience, and a strong commitment to seeing that Loyola's health sciences continue to excel and exceed the standard for academic and research excellence. For more on the HSD, visit LUC.edu/hsd.