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1.
Biomed Pharmacother ; 58 Suppl 1: S129-34, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15754851

ABSTRACT

A test of the relative merits of timed melatonin for the treatment of cardiac ischemia as well as hypertension refractory to other drugs is documented against the background of earlier chronobiological studies on blood pressure (BP), disease risks, circadian hyper-amplitude-tension and melatonin effects broadly.


Subject(s)
Blood Pressure/drug effects , Hypertension/drug therapy , Melatonin/therapeutic use , Myocardial Ischemia/drug therapy , Treatment Failure , Animals , Blood Pressure/physiology , Chronotherapy/methods , Follow-Up Studies , Humans , Hypertension/physiopathology , Melatonin/administration & dosage , Meta-Analysis as Topic , Myocardial Ischemia/physiopathology
2.
J Circadian Rhythms ; 1(1): 2, 2003 Oct 29.
Article in English | MEDLINE | ID: mdl-14728726

ABSTRACT

Afew puzzles relating to a small fraction of my endeavors in the 1950s are summarized herein, with answers to a few questions of the Editor-in-Chief, to suggest that the rules of variability in time complement the rules of genetics as a biological variability in space. I advocate to replace truisms such as a relative constancy or homeostasis, that have served bioscience very well for very long. They were never intended, however, to lower a curtain of ignorance over everyday physiology. In raising these curtains, we unveil a range of dynamics, resolvable in the data collection and as-one-goes analysis by computers built into smaller and smaller devices, for a continued self-surveillance of the normal and for an individualized detection of the abnormal. The current medical art based on spotchecks interpreted by reference to a time-unqualified normal range can become a science of time series with tests relating to the individual in inferential statistical terms. This is already doable for the case of blood pressure, but eventually should become possible for many other variables interpreted today only based on the quicksand of clinical trials on groups. These ignore individual differences and hence the individual's needs. Chronomics (mapping time structures) with the major aim of quantifying normalcy by dynamic reference values for detecting earliest risk elevation, also yields the dividend of allowing molecular biology to focus on the normal as well as on the grossly abnormal.

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