| Literature DB >> 1855673 |
Abstract
Oral contraceptive (OC) use is a risk for thrombogenic events. This paper reviews effects of OC on oxidative status, coagulation, and platelet activity. Complicating effects of cardiovascular risk factors such as smoking, diabetes, hyperpidemia, and hypertension, are discussed. From these data we conclude that: 1. OC use modifies slightly but significantly the oxidative status in women and in animals by decreasing in plasma and blood cells the antioxidant defenses (vitamins and enzymes). 2. The changes in the oxidative status are related to an increase in plasma lipid peroxides apparently responsible for the hyperaggregability and possibly the imbalance in clotting factors associated with the OC-induced prethrombotic state. 3. These effects of OC appear to be increased by a high intake of polyunsaturated fat and counteracted by supplements of vitamin E. 4. The risk factors acting synergistically with OC, have all been shown to increase platelet reactivity. In addition, smoking, diabetes, and, to some extent, dyslipidemia are associated with an increased level of lipid peroxides and concomitant changes in the antioxidant defenses that can be additive to those induced by OC. Thus, free radicals and lipid peroxidation could be the underlying mechanism in the predisposition to thrombosis induced by most risk factors in OC users. 5. Results of epidemiologic and experimental studies in this field will be concordant only when diet and natural antioxidants will be systematically taken into consideration.Entities:
Keywords: Behavior; Biology; Cardiovascular Effects--etiology; Contraception; Contraceptive Methods--contraindications; Contraceptive Methods--pharmacodynamics; Family Planning; Hematological Effects; Hemic System; Lipids; Oral Contraceptives, Combined--contraindications; Oral Contraceptives, Combined--pharmacodynamics; Oral Contraceptives--contraindications; Oral Contraceptives--pharmacodynamics; Physiology; Platelet Aggregation; Risk Factors; Smoking; Vitamins
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Year: 1991 PMID: 1855673 DOI: 10.1016/0891-5849(91)90039-6
Source DB: PubMed Journal: Free Radic Biol Med ISSN: 0891-5849 Impact factor: 7.376