John David Spence

John David Spence
Born (1944-11-10) November 10, 1944
Peru, Talara
Known for Father of carotid plaque measurement

John David Spence (born November 10, 1944) is a Canadian medical doctor, medical researcher and professor at the University of Western Ontario. Along with his affiliation with the University of Western Ontario (where he teaches Clinical Neurological Science) he is affiliated with the London Health Sciences Centre’s University Hospital (where he has set up and runs stroke prevention clinics) and the Robarts Research Institute, one of Canada’s leading medical research organizations. He is a recognized expert in stroke prevention and stroke prevention research and has over 400 peer-reviewed publications since 1970. He has delivered more than 500 lectures in 37 countries to physicians around the world. Recently, he has received the Research Excellence Award from the Canadian Society for Atherosclerosis, Thrombosis and Vascular Biology.

Dr. Spence is the director of the Stroke Prevention & Atherosclerosis Research Centre (SPARC) located at the Robarts Research Institute. With Maria Dicicco, RVT, he pioneered the measurement of total plaque area (TPA) in a patient’s carotid artery using ultrasound technology. The ability to measure TPA gives doctors the ability to treat, and measure the change in, the amount of plaque in a patient’s arteries and has given researchers the ability to measure the effectiveness of new drug treatment therapies for stroke prevention.[1] Dr. Spence is recognized as “The Father of Total Plaque Area Measurement” and the importance of TPA measurement is, in Dr Spence’s words, “We can now treat arteries instead of just treating risk factors”.

Spence - Key Research Discoveries

Cerebral consequences of hypertension: treating high blood pressure prevents only arteriolar strokes. (.[2]) This research led to the understanding that the effects of therapies, designed to reduce hypertension, on blood pressure need to be distinguished from other effects on atherosclerosis.

Effects of antihypertensive drugs on blood velocity and arterial flow disturbances 1976, 1980, 1995: these studies showed that antihypertensive drugs have different effects on blood velocity and arterial flow disturbances, which have implications for how effective they are at fighting the buildup of arterial plaque. (.[3])

Effects of grapefruit juice on drug metabolism: The discovery with Drs. David Bailey and Malcolm Arnold, that grapefruit juice markedly increases blood levels of a number of drugs that have low bioavailability because of gut wall first-pass metabolism by CYP3A4 made a major contribution to the understanding of pharmacokinetics, and has opened up a new field of pharmacology. ([4]).

Ultrasound measurement of plaque: Beginning in 1990, Dr. Spence pioneered the use of carotid plaque measurement (as opposed to intima-media thickness) for research and for management of patients with carotid artery disease. (.[5]). This has evolved to the use of 3-D plaque volume measurements for evaluation of new therapies. The effect of drug therapies on carotid plaque volume can now be evaluated in a very cost-effective way.

Development of quantitative traits for human atherosclerosis: Spence developed a number of quantitative traits that will advance the search for new genetic causes of atherosclerosis, and thus new therapeutic targets and new therapies for atherosclerosis. These are unexplained atherosclerosis and its progression, unexplained protection from atherosclerosis and unexplained regression of atherosclerosis. (;.[6][7][8])

Appropriate carotid endarterectomy: Showed in 2005 ([9]) that with intensive medical therapy most patients with asymptomatic carotid stenosis cannot benefit from endarterectomy or stenting, and that the very small proportion (10%) who may benefit can be identified by microembolus detection on transcranial Doppler. Showed in 2010 ([10]) that the proportion who could benefit had declined with more intensive therapy to less than 5%. SPARC’s work has recently been confirmed by an international multicenter study. Dr. Spence is now leading a study in the Canadian Atherosclerosis Imaging Network, on histological validation of imaging features of vulnerable plaque and it will also serve to identify high-risk carotid plaques.

Special Projects

  1. Member of the “Joint Stroke Working Group” set up by the Ministry of Health and the Heart and Stroke Foundation.
  2. Member of the Shape Task Force II which is recognized in the U.S. Centers of Excellence program in their work for heart attack prevention and eradication.
  3. National stroke prevention program of the Argentina health organization training Argentinean physicians in vascular prevention.

Education and Training

  1. Ridley College.
  2. M.D. University of Western Ontario.
  3. Clinical Pharmacology training at the Cardiovascular Research Institute of the University of California at San Francisco.
  4. M.B.A. from the University of Toronto.
  5. Trained with Henry J. M. Barnett at University Hospital in London Ontario. Dr. Barnett is a leading stroke researcher who pioneered the use of aspirin in stroke prevention therapy.

See also

Spence is the great-grandson of David Spence (Canadian Politician) and trained with Henry J. M. Barnett

References

  1. ↑ Spence JD, et al. Carotid Plaque Area: A Tool for Targeting and Evaluating Vascular Preventive Therapy Stroke. 2002;33:2916-2922
  2. ↑ Stroke 1986; 17(5):808-10
  3. ↑ Magn Reson Med Jan 2002;47:149-159
  4. ↑ Lancet 1991; 337(8736):268-9
  5. ↑ Spence JD, et al. Carotid Plaque Area: A Tool for Targeting and Evaluating Vascular Preventive Therapy Stroke. 2002;33:2916-2922
  6. ↑ Stroke 1999;30:969-73; Atherosclerosis 1999;144:429-340
  7. ↑ Stroke 2003;34:1178-1182, Nature Clinical Practice Neurology 2006;2: 611-619
  8. ↑ Lanktree MB, Hegele RA, Schork NJ, Spence JD. Extremes of unexplained variation as a phenotype: an efficient approach for genome-wide association studies of cardiovascular disease. Circ Cardiovasc Genet Apr 2010; 3: 215 – 221
  9. ↑ Stroke 2005;36:2373-2378
  10. ↑ Arch Neurol. 2010 Feb; 67(2):180-6
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