Long-term oral anticoagulation reduces bone mass in patients with previous hemispheric infarction and nonrheumatic atrial fibrillation

Abstract

Background and Purpose: Vitamin K is an essential factor for synthesis of plasma clotting proteins and for site-specific carboxylation of bone Gla protein and other bone matrix proteins. Low vitamin K has been associated with reduced bone mineral density. Warfarin therapy, which inhibits vitamin K-dependent blood-clotting, has been demonstrated to reduce the risk of stroke in nonrheumatic atrial fibrillation. We evaluated vitamin K and bone mineral density in nonrheumatic atrial fibrillation patients who had long- term warfarin therapy after an ischemic stroke. Methods: Sera were collected from 64 patients with non-rheumatic atrial fibrillation and ischemic stroke who had been treated with warfarin, 63 stroke patients without warfarin, and 39 control subjects. All stroke patients in both groups had hemiplegia. Sera were assayed for vitamins K1 and K2, bone Gla protein, and 25- hydroxyvitamin D. Bone mineral density was determined in both second metacarpals. Results: Serum vitamin K1 concentrations (ng/mL) were lower in treated patients (.234±.177 ng/mL) than in untreated patients (.329±.284) or controls (.553±.164). Bone Gla protein was lower in treated patients' sera (1.241±.799 ng/mL) than in untreated patients (4.476±3.226). Concentrations of 25-hydroxyvitamin D were lower in both patient groups. Bone mineral density was lower on both sides in treated patients than in untreated patients (P