Warin A P, Greaves M W, Gatecliff M, Williamson D M, Warin R P
Br J Dermatol. 1980 Oct;103(4):405-9. doi: 10.1111/j.1365-2133.1980.tb07263.x.
Nine patients with hereditary angio-oedema (H.A.E.) with a deficiency of C1 esterase inhibitor (C1 INH), have been treated with low dose attenuated androgenic drugs, with complete control of their disease. The C1 esterase inhibitor and C4 levels became normal in only one patient. It is concluded that H.A.E. can be controlled in the absence of correction of the reduced levels of C1 INH and C4. The mode of action of these drugs appears to be more complex than is generally realized.
9名患有遗传性血管性水肿(H.A.E.)且C1酯酶抑制剂(C1 INH)缺乏的患者,接受了低剂量减毒雄激素药物治疗,其病情得到了完全控制。只有1名患者的C1酯酶抑制剂和C4水平恢复正常。得出的结论是,在未纠正C1 INH和C4水平降低的情况下,遗传性血管性水肿也可以得到控制。这些药物的作用方式似乎比一般认为的更为复杂。