Gregory T. Macaskill
University of Melbourne
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Featured researches published by Gregory T. Macaskill.
Acta geneticae medicae et gemellologiae: twin research | 1992
John L. Hopper; Victoria White; Gregory T. Macaskill; David J. Hill; Clifford Ca
In 1988, questionnaires were received from 1,400 twin pairs (17% MZM, 23% MZF, 17% DZM, 19% DZF, 24% DZO) aged 11 to 18, registered with the Australian NHMRC Twin Registry. Twins reported independently on themselves and on the perceived behaviour of their parents, siblings and friends. For smoking and for drinking in the previous month, the prevalence was modelled as a logistic function of age, sex, perceived smoking or drinking behaviour of family and friends, and the Adult Eysenck Personality Questionnaire (AEPQ) scales. Strengths of association were: family behaviour, odds ratio (OR) Language: en
Journal of Hypertension | 1990
Trefor Morgan; Adrianne Anderson; Peter McDonald; John L. Hopper; Gregory T. Macaskill
Mortality from coronary artery disease is a common problem in treated hypertensive patients, and these people have a high prevalence of elevated cholesterol levels. A study was undertaken to determine whether cholesterol could be lowered effectively without major side effects in patients with treated hypertension. Forty-nine patients (mean age 67.6 years) with cholesterol>5.5 mmol/l were placed on a reduced-fat (< 30% of calories from fat with a ratio of polyunsaturated to saturated fats of<1) diet for 3 months. If the cholesterol was between 5.5 and 7.5 mmol/l and total cholesterol divided by high-density lipoprotein cholesterol was >4.5, the patients were randomly allocated either to the simvastatin (24 patients) or the placebo group (25 patients). Diet and placebo caused minor and insignificant falls in cholesterol and no change in triglycerides or lipids. Treatment with simvastatin reduced cholesterol levels from 6.85 to 4.75 mmol/l (P<0.001), triglycerides from 2.7 to 2.1 mmol/l (P<0.01), low-density lipoproteins from 4.6 to 2.6 mmol/l (P<0.001) and high-density lipoproteins rose from 1.09 to 1.18 mmol/l (P<0.01). Total cholesterol divided by high-density lipoprotein cholesterol fell from 6.3 to 4.0 (P<0.001) The drug was well tolerated and the side-effect profile did not differ from the placebo in clinical or biochemical events. The active drug was stopped in one patient (abdominal pain, dizziness, headache, tiredness) and in two patients taking the placebo (elevated creatine phosphokinase, cardiovascular collapse) Simvastatin effectively lowered total cholesterol and improved the lipoprotein profile. The dose required in most patients was 40 mg/day. Simvastatin may be an acceptable drug to improve the lipoprotein profile in order to determine whether this improves the prognosis in patients treated for hypertension
The Journal of Clinical Endocrinology and Metabolism | 1991
Paul J. Kelly; John L. Hopper; Gregory T. Macaskill; Nicholas Pocock; Philip N. Sambrook; John A. Eisman
Genetic Epidemiology | 1990
John L. Hopper; Murray C. Hannah; Gregory T. Macaskill; John D. Mathews; D. C. Rao
Journal of Applied Physiology | 1991
John L. Hopper; M. E. Hibbert; Gregory T. Macaskill; P. D. Phelan; L. I. Landau
Journal of Studies on Alcohol and Drugs | 1991
John Powles; Gregory T. Macaskill; John L. Hopper; Ktenas D
Acta geneticae medicae et gemellologiae | 1992
John L. Hopper; Victoria White; Gregory T. Macaskill; David J. Hill; Clifford Ca
Journal of Human Hypertension | 1993
John Powles; John L. Hopper; Gregory T. Macaskill; Ktenas D
Acta geneticae medicae et gemellologiae: twin research | 1990
John L. Hopper; John B. Carlin; Gregory T. Macaskill; Peter L. Derrick; Louisa Flander; Graham G. Giles
Acta geneticae medicae et gemellologiae | 1993
John L. Hopper; Victoria White; Gregory T. Macaskill; David J. Hill; Clifford Ca