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For full versions of posted research articles readers are encouraged to email requests for "electronic reprints" (text file, PDF files, FAX copies) to the corresponding or lead author, who is highlighted in the posting.

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Friday, September 19, 2008

NIH News release - Li to Step Down as Director of the National Institute on Alcohol Abuse and Alcoholism

Bethesda, Maryland — Ting-Kai Li, M.D., director of the National Institute on Alcohol Abuse and Alcoholism (NIAAA) since November 2002, announced today that he will step down from his post and retire from Federal service, effective October 31, 2008. Kenneth R. Warren, Ph.D., the NIAAA Deputy Director since February 2008, will serve as Acting Director of the Institute while a search for a new Director is initiated.


“I leave NIAAA/NIH feeling that my tenure has resulted in greater transparency, accountability, trust, and stability of funding for alcohol research. Research supported by NIAAA in the past 5 years has reframed our understanding of alcohol dependence in several ways by demonstrating that it is a developmental disorder that has its roots in childhood and adolescence. While initiation of drinking is largely influenced by peer and family environmental factors, the transition to habitual and dependent drinking is strongly influenced by genetic factors. This has important prevention and treatment implications.”


During Dr. Li’s tenure, NIAAA issued a rolling 5-year strategic plan for NIAAA; provided administrative leadership to achieve stability in NIAAA’s success rate for research grants; increased support for new investigators; engaged the NIAAA in the NIH Roadmap for Medical Research; emphasized a multi- and transdisciplinary approach to alcohol research and the study of gene-environment interactions. Finally, he guided the analysis of data showing that measures of an individual’s pattern of drinking are the best indicators of alcohol problems, in much the same way that numerical measurements of blood pressure, cholesterol and triglycerides relate to relative risk for cardiovascular disease.

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