M. L. O. Shea
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
M. L. O. Shea has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
B. H. Mulsant
Centre for Addiction and Mental Health, Toronto, ON
1 shared publicationC. F. Reynolds
Department of Psychiatry and Department of Behavioral and Community Health Sciences, University of Pittsburgh School of Medicine and Graduate School of Public Health, Pittsburgh, PA
1 shared publicationD. Dixon
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO
1 shared publicationE. J. Lenze
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO
1 shared publicationL. D. Garfield
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO
1 shared publicationP. Doré
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO
1 shared publication
Latest Publications
- 29 January 2013
- Published by Springer Nature in Osteoporosis International
- Vol. 24 (5) , 1741-1749
Serotonin–norepinephrine reuptake inhibitor therapy in late-life depression is associated with increased marker of bone resorption
Antidepressants are associated with bone loss and fractures in older adults. We treated depressed older adults with an antidepressant and examined its effects on bone turnover by comparing blood samples before and after treatment. Bone resorption increased after antidepressant treatment, which may increase fracture risk.
- 29 January 2013
- Published by Springer Nature in Osteoporosis International
- Vol. 24 (5) , 1741-1749
Serotonin–norepinephrine reuptake inhibitor therapy in late-life depression is associated with increased marker of bone resorption
Antidepressants are associated with bone loss and fractures in older adults. We treated depressed older adults with an antidepressant and examined its effects on bone turnover by comparing blood samples before and after treatment. Bone resorption increased after antidepressant treatment, which may increase fracture risk.