Department of Medicine
Faculty Profiles by Division

Department of Medicine

Faculty Profiles

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photo Erin E. Kershaw, MD

Endocrinology and Metabolism

Chief, Division of Endocrinology and Metabolism

Associate Professor of Medicine

Endowed Chair for Obesity and Diabetes Research

Email: endoadm@pitt.edu

Contact
Office: W1055 Biomedical Science Tower
200 Lothrop Street
Pittsburgh, PA 15213
 
E-mail: endoadm@pitt.edu
Education and Training
Education
BA, Cornell University College of Arts and Sciences, 1991
MD, Weill Cornell Medical College of Cornell University, 1997
Training
Intern, Department of Medicine, New York Presbyterian Hospital- Cornell Campus, 1998
Resident, Department of Medicine, New York Presbyterian Hospital- Cornell Campus, 2000
Fellow, Division of Endocrinology, Department of Medicine, Beth Israel Deaconess, 2003
Instructor, Division of Endocrinology, Department of Medicine, Beth Israel Deaconess, 2008
Research Interest
Dr. Kershaw's academic mission is to forward the understanding and treatment of obesity and related metabolic disorders by combining basic and translational research with clinical expertise. Obesity is a global public health threat that is frequently associated with additional metabolic abnormalities including insulin resistance, glucose intolerance, dyslipidemia, and hypertension (the metabolic syndrome). Together these abnormalities contribute to diseases affecting virtually every organ system. Dr. Kershaw's laboratory focuses on defining the mechanisms by which intracellular lipid metabolism (synthesis, storage, hydrolysis, and oxidation) contributes to obesity and associated metabolic disorders. Most recently, Dr. Kershaw's research efforts have focused on pathways of triacylglycerol hydrolysis (lipolysis) – arguably one of the most fundamental processes in metabolism. Dr. Kershaw is working to define how tissue-specific triacylglycerol hydrolysis contributes to metabolic phenotypes, not only in the metabolic syndrome, but also in variety of other diseases ranging from infertility to cancer. Another major focus of her laboratory is to identify and characterize additional proteins and pathways that contribute to metabolic disease. These efforts fall into two main areas: 1) characterizing novel adipocyte-secreted factors (adipokines) and their relationship to metabolic disease in humans, and 2) characterizing novel genes/loci linked to metabolic disease in humans. Dr. Kershaw's laboratory uses a combination of molecular, cellular, physiological, and translational approaches. The ultimate goal is to develop more effective strategies for prevention and treatment of obesity and associated metabolic disorders.
Clinical Interest
Dr. Kershaw's clinical interests focus on disorders of "fat," including the following core areas: 1) obesity, insulin resistance, diabetes, and metabolic syndrome, 2) pre- and post-operative care for bariatric surgery patients, 3) lipodystrophies, lipomatoses, and rare adipose tissue disorders, and 4) lipid metabolism and dyslipidemias. Dr. Kershaw is board certified in 1) Endocrinology, Diabetes, and Metabolism by the American Board of Internal Medicine (ABIM), 2) Obesity Medicine by the American Board of Obesity medicine (ABOM), and Clinical Lipidology by the American Board of Clinical Lipidology (ABCL).
Educational Interest
Dr. Kershaw's educational mission is to facilitate the career development of trainees in the field of Endocrinology and Metabolism with an emphasis on obesity and its complications. She accomplishes this mission through a combination of didactic coursework, hands-on training, and mentoring. In this way, Dr. Kershaw, has contributed to the scientific and academic development of several trainees ranging from undergraduate students to trainees at the T32 and K level. Several of her prior trainees have subsequently secured independent tenure-track research positions, academic positions, and/or positions in pharmaceutical companies. Dr. Kershaw has held several research training leadership positions including serving as the Associated Program Director for Research for the Clinical Adult Endocrine Fellowship Program, as an oversight committee member for the T32 Training Program in Endocrinology, and as a member of the Physician Scientist Training Program Steering Committee at t he University of Pittsburgh.
Publications
For my complete bibliography, Click Here.
Selected Publications:
Harmon, D. B., Wu, C., Dedousis, N., Sipula, I. J., Stefanovic-Racic, M., Schoiswohl, G., O'Donnell, C. P., Alonso, L. C., Kershaw, E. E., Kelley, E. E., O'Doherty, R. M. Adipose Tissue Derived Free Fatty Acids Initiate Myeloid Cell Accumulation in Mouse Liver in States of Lipid Oversupply. Am J Physiol Endocrinol Metab. 2018; Epub ahead of print.
Parajuli, N., Takahara, S., Matsumura, N., Kim, T. T., Feraoussi, M., Migglautsch, A. K., Zechner, R., Breinbauer, R., Kershaw, E. E., Dyck, J. R. B. Atglistatin Ameliorates Functional Decline in Heart Failure via Adipocyte-specific Inhibition of Adipose Triglyceride Lipase. Am J Physiol Heart Circ Physiol. 2018; Epub ahead of print.
Babaei, R., Schuster, M., Meln, I., Lerch, S., Ghandour, R. A., Pisani, D. F., Bayindir-Buchhalter, I., Marx, J., Wu, S., Schoiswohl, G., Billeter, A. T., Krunic, D., Mauer, J., Lee, Y. H., Granneman, J. G., Fischer, L., Muller-Stitch, B. P., Amri, E. Z., Kershaw, E. E., Heikenwalkder, M. Jak-TGFß cross-talk links transient adipose tissue inflammation to beige adipogenesis. Sci Signal. 2018; 11(527).
Kotzbeck, P., Giordano, A., Mondini, E., Murano, I., Severi, I., Venema, W., Cecchini, M. P., Kershaw, E. E., Barbatelli, G., Haemmerle, G., Zechner, R., Cinti, S. Brown adipose tissue whitening leads to brown adipocyte death and adipose tissue inflammation. J Lipid Res. 2018; 59(5): 784-794.
Salatzki, J., Foryst-Ludwig, A., Bentele, K., Blumrich, A., Smeir, E., Ban, Z., Brix, S., Grune, J., Beyhoff, N., Klopfleisch, R., Dunst, S., Surma, M. A., Klose, C., Rothe, M., Heinzel, F. R., Krannich, A., Kershaw, E. E., Beule, D., Schulze, P.C., Marx, N. Adipose tissue ATGL modifies the cardiac lipidome in pressure-overload-induced left ventricular failure. PLoS Genet. 2018; 14(1): e1007171.
Schreiber, R., Diwoky, C., Schoiswohl, G., Feiler, U., Wongsiriroj, N., Abdellatif, M., Kolb, D., Hoeks, J., Kershaw, E. E., Sedej, S., Schrauwen, P., Haemmerle, G., Zechner, R. Cold-Induced Thermogenesis Depends on ATGL-Mediated Lipolysis in Cardiac Muscle, but Not Brown Adipose Tissue. Cell Metab. 2017; 26(5): 753-763.e7.
Simcox, J., Geoghegan, G., Maschek, J. A., Bensard, C. L., Pasquali, M., Miao, R., Lee, S., Jiang, L., Huck, I., Kershaw, E. E., Donato, A. J., Apte, U., Longo, N., Rutter, J., Schreiber, R., Zechner, R., Cox, J., Villanueva, C. J. Global Analysis of Plasma Lipids Identifies Liver-Derived Acylcarnitines as a Fuel Source for Brown Fat Thermogenesis. Cell Metab. 2017; 26(3): 509-522.
Falabella, M., Sun, L., Barr, J., Pena, A. Z., Kershaw, E. E., Gingras, S., Goncharova, E. A., Kaufman, B. A. Single-Step qPCR and dPCR detection of diverse CRISPR-Cas9 gene editing events in vivo. G3 (Bethesda). 2017; 7(10): 3533-3542.
Kim, S. P., Li, Z., Zoch, M. L., Frey, M. L., Bowman, C. E., Kushwaha, P., Ryan, K. A., Goh, B. C., Scafidi, S., Pickett, J. E., Faugere, M. C., Kershaw, E. E., Thoreck, D. L. J., Clemens, T. L., Wolfgang, M. H., Riddle, R. C. Fatty acid oxidation by the osteoblast is required for normal bone acquisition in a sex- and diet-dependent manner. JCI Insight. 2017; 2(16).
Rachakonda, V., Wills, R., DeLany, J. P., Kershaw, E. E., Behari, J. Differential impact of weight loss on nonalcoholic fatty liver resolution in a North American cohort with obesity. Obesity (Silver Spring). 2017; Epub ahead of print.
Sponsored Research/Activities
Title: Investigating the role of adipose tissue in mobility and aging (SOMMA-AT)
Role: Principal Investigator
Funding Agency: AdventHealth / National Institute of Health
Grant Number: R56 AG066474
Start Year: 2020
End Year: 2025
Title: Overcoming Insulin Deficiency and Resistance to Reduce Diabetes Risk
Role: Principal Investigator
Funding Agency: Pittsburgh Foundation
Grant Number: RES
Start Year: 2020
End Year: 2021
Title: Molecular Transducers of Physical Activity Clinical Centers
Role: Co-Investigator
Funding Agency: National Institute of Arthristis, Muscoskel, & Skin Disease
Grant Number: U01 AR071130
Start Year: 2016
End Year: 2021
Title: Integrated Cellular, Mouse and Human Research on a Missense Variant Influencing Adiposity in Samoans
Role: Co-Investigator
Funding Agency: Brown University/ National Institute of Diabetes, Digestive, & Kidney Disease
Grant Number: R01 DK090166
Start Year: 2016
End Year: 2020
Title: Human Microphysiology Systems Disease Model of Type 2 Diabetes Starting with Liver and pancreatic Islets
Role: Collaborator
Funding Agency: National Institute of Diabetes, Digestive, & Kidney Disease
Grant Number: UG3 DK119973
Start Year: 2018
End Year: 2020
Notable Achievements
Howard Hughes Medical Institute (HHMI), Physician-Scientist Early Career Award, 2009
Endocrine Fellows Foundation, Endocrine Fellow Research Award, 2002
The Endocrine Society, Honorary Membership Award for Endocrine Research and Education, 1997
Cornell University Medical College, Janet M. Glasgow Memorial Achievement Award, 1997
Cornell University Medical College, Medical Doctorate with Honors in Research, 1997
Cornell University Medical College, Alpha Omega Alpha Medical Honor Society, 1996
Howard Hughes Medical Institute (HHMI), Award for Continuation of Medical Studies (year 2), 1996
Howard Hughes Medical Institute (HHMI), Award for Continuation of Medical Studies (Year 1), 1995
Cornell University Medical College, Dean's Research Award, 1995
Cornell University Medical College, Dr. Harold Lamport Biomedical Research Award, 1994