Peter J. Schwartz - Bio


Professor and Chairman, Department of Cardiology, Policlinico San Matteo IRCCS, Pavia, Italy

Dr Peter J. Schwartz, MD, graduated in Medicine in 1967 at the University of Milan (Italy).
He is Professor and Chairman of Cardiology at the University of Pavia, Chief of the Coronary Care Unit at Policlinico San Matteo, Pavia (Italy), Professor of Physiology andBiophysics at the University of Oklahoma (OK, USA), Extraordinary Professor in Internal Medicine at the University of Stellenbosch, South Africa, and Honorary Professor in Internal Medicine at the University of Capetown, South Africa. From January 1999 to December 2000 he was the President of the Italian Society of Cardiology and from 1988
to 1992 the Chairman of the Working Group on Arrhythmias of the European Society of Cardiology.

Dr Schwartz's main area of research has always been Sudden Cardiac Death, from different angles including pathophysiology, risk stratification, therapeutic approaches,
and genetic mechanisms.

Dr Schwartz has extensively investigated the relationship between the autonomic nervous system and life-threatening arrhythmias. Beginning with his first article in 1969 he has
contributed to the study of cardiac reflexes, has developed the concept of sympathetic imbalance and has extensively studied the pathophysiologic effects and the therapeutic
efficacy of left cardiac sympathetic denervation, which he has proved to be a powerful tool for the prevention of ventricular fibrillation triggered by sympathetic activation.

Dr Schwartz has pioneered the study of autonomic markers (especially baroreflex sensitivity) for the identification of individuals at high risk for sudden death.
His experimental findings of the early eighties have evolved in a landmark prospective clinical trial (ATRAMI) involving 1,300 patients. This study has provided the first evidence
that autonomic reflexes can indeed contribute to post myocardial infarction risk stratification. His concepts and findings have paved the way for the now innumerable studies on the prognostic value of autonomic markers.

For 35 years he has relentlessly investigated in detail the congenital long QT syndrome (LQTS), of which he is regarded by many as the leading expert. In 1979, in partnership with Dr Arthur Moss, he initiated the International Registry for LQTS which - over 25 years of continued efforts - has contributed to define the multiple clinical characteristics of the disease and its natural history, and has made possible the identification of the major disease genes by providing the molecular biologists with clearly defined clinical phenotypes of affected and unaffected individuals from large families. In 1980 he advanced the unorthodox hypothesis that some patients affected by LQTS might have had a normal QT interval, thus stretching to the limits the concept of phenotypic heterogeneity; almost 20 years later molecular studies by his own group proved the existence of "low penetrance" in LQTS and confirmed his original hypothesis.

Dr Schwartz has recently contributed to the understanding of the relation between genotype and phenotype in LQTS, providing the basis for the development of gene-specific therapy and, with his partners, has just identified the first genetic modifier for the clinical severity of LQTS. He remains entirely committed to the elucidation of this unique disease
and continues to manage personally the patients affected by LQTS.

In 1976 he hypothesized that one of the causes of the Sudden Infant Death Syndrome (SIDS) could be a life-threatening arrhythmia due to mechanisms similar to those present
in the long QT syndrome. To test the hypothetical correlation between prolonged QT interval and SIDS he designed and initiated a prospective study based on ECG recordings
in newborns, which was carried out without funding and lasted 18 years.
This study demonstrated that a QT interval prolongation in the first week of life constitutes a major risk factor for SIDS. Subsequently, Dr Schwartz and his research group provided
the first demonstration of the molecular link between LQTS and SIDS, which represented the "proof of concept" for this relation. His most recent data on 200 SIDS victims suggest
that LQTS mutations are present in approximately 10-12% of SIDS victims.
As these deaths could be prevented by therapy with beta-blockers, if early diagnosis is made, the findings support the idea - championed by Dr Schwartz for many years - of widespread neonatal ECG screening, another controversial concept.

Over the years Dr Schwartz has received a large number of major recognitions. In 1993 he gave the "Grüntzig lecture", traditionally offered to a member of the European Society of Cardiology who has made special contributions to Cardiology. In 1994 the American
Heart Association invited him to give the "Paul Dudley White International Lecture",41 which is regarded as the greatest sign of recognition given to non-American investigators.
In 1995 he became the 4th Fourth Gordon K. Moe Visiting Professor at the Masonic Medical Research Laboratory, Utica, NY in recognition of his "outstanding contributions to science and medicine in the fields of clinical and basic cardiology". On May 1999 he gave the keynote talk at the opening plenary session of the 20th Annual Scientific Sessions of NASPE. In 2001 he received the "Michel Mirowski Award" for his work on sudden cardiac death, and on May 5 during NASPE's 22nd Annual Scientific Session in
Boston he received the "Distinguished Scientist Award 2001" for his "contribution to the advancement of scientific knowledge in the field of cardiac electrophysiology".

Dr Schwartz is the only European investigator with uninterrupted funding for his research activity from the National Institutes of Health (NIH); his first grant was funded in 1974 and the last goes through 2006.

Dr Schwartz serves the leading cardiology journals as a member of the Editorial Board or as a reviewer. He is the author of more than 1100 publications including 346 original
articles, 12 books, and 141 chapters. His Impact Factor in the last seven years was 734.