Diagnosis of von Willebrand's disease: A comparative study of diagnostic tests on nine families with von Willebrand's disease and its differential diagnosis from hemophilia and thrombocytopathy

• Published in: The American journal of medicine Vol. 60; no. 3; pp. 344 - 356
• Main Authors: Lian, Eric Chun-Yet, Deykin, Daniel
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.1976
• Subjects: Antigens - analysis; Blood Coagulation Tests; Blood Platelet Disorders - diagnosis; Diagnosis, Differential; Factor VIII - analysis; Female; Hemophilia A - diagnosis; Heterozygote; Humans; Male; Pedigree; Platelet Adhesiveness; Platelet Aggregation; Ristocetin; von Willebrand Diseases - blood; von Willebrand Diseases - diagnosis; von Willebrand Diseases - genetics
• ISSN: 0002-9343; 1555-7162
• DOI: 10.1016/0002-9343(76)90750-6

Nine probands with von Willebrand's disease, and their family members, totalling 43 people, were examined. Twenty-seven had a history of bleeding; 29 had an increased factor VIII activity:factor VIII related antigen ratio; 24 had a decreased factor VIII related antigen; 23 had a prolonged bleeding time; 19 had a reduced platelet adhesiveness; 16 had a decreased factor VIII activity; and 14 had an abnormal ristocetin-induced platelet aggregation. Eight members with both normal bleeding time and normal factor VIII activity were found to have other abnormal tests: elevated ratio of factor VIII activity to factor VIII related antigen in seven; decreased factor VIII related antigen in four; and reduced platelet adhesiveness in one. Therefore, ratio of factor VIII activity to factor VIII related antigen and factor VIII related antigen are more sensitive and may be used for the detection of heterozygous carriers of von Willebrand's disease. Although patients with thrombocytopathy may have a prolonged bleeding time, decreased platelet adhesiveness and reduced platelet aggregation by ristocetin, their factor VIII activity, factor VIII related antigen and ratio of factor VIII activity to factor VIII related antigen are normal and their abnormal ristocetin test cannot be corrected by the addition of factor VIII concentrate. Hemophilic subjects and hemophilic carriers, who are deficient in factor VIII activity, usually have a normal bleeding time, normal platelet adhesiveness, and normal ristocetin test. In contrast to patients with von Willebrand's disease, their factor VIII related antigen is normal or slightly increased and their ratio of factor VIII activity to factor VIII related antigen is significantly reduced. We conclude that ratio of factor VIII activity to factor VIII related antigen and factor VIII related antigen are not only more sensitive but also more specific for the diagnosis of von Willebrand's disease.