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睾酮治疗可能与血栓形成倾向相互作用,导致骨坏死。

Testosterone Therapy Can Interact With Thrombophilia, Leading to Osteonecrosis.

作者信息

Glueck Charles J, Riaz Rashid, Prince Marloe, Freiberg Richard A, Wang Ping

出版信息

Orthopedics. 2015 Dec;38(12):e1073-8. doi: 10.3928/01477447-20151120-03.

Abstract

Although this effect is not widely recognized, testosterone therapy can interact with thrombophilia, causing osteonecrosis. In 12 men and 4 women who had idiopathic osteonecrosis a median of 6 months after the onset of testosterone therapy, the authors examined the interaction between testosterone therapy and previously undiagnosed thrombophilia. The authors hypothesized that patients who had osteonecrosis after starting testosterone therapy were more likely than 110 normal control subjects or 48 patients who had osteonecrosis and were not receiving testosterone therapy to have thrombophilia. Measures of thrombophilia included Factor V Leiden, prothrombin, PAI-1 gene mutations, Factor VIII, Factor XI, anticardiolipin antibody immunoglobulin G or immunoglobulin M, and homocysteine values. In 10 cases, osteonecrosis occurred 6 months or less after the onset of testosterone therapy, and in all 16 cases, it occurred after a median of 6 months of testosterone therapy. Of the 16 cases, 5 (31%) were Factor V Leiden heterozygotes vs 2 of 109 (2%) healthy control subjects (P=.0003) and 4 of 48 patients who had osteonecrosis and were not receiving testosterone therapy (P=.04). Of the 16 cases, 4 (25%) had high (>150%) Factor VIII levels vs 7 of 103 (7%) healthy control subjects (P=.04), and 3 (19%) had high (>150%) Factor XI levels vs 3 of 101 (3%) healthy control subjects (P=.03). Of the 16 patients with osteonecrosis, 14 (88%) had at least 1 abnormal procoagulant value (of the 8 measured) vs 47 of 110 (43%) healthy control subjects (P=.0009). Of the 5 men whose serum estradiol level was measured while they were receiving testosterone therapy, this level was high (≥42.6 pg/mL) in 4. When testosterone therapy is given to patients with thrombophilia, they are at increased risk for osteonecrosis.

摘要

尽管这种效应尚未得到广泛认可,但睾酮治疗可能与血栓形成倾向相互作用,导致骨坏死。在12名男性和4名女性中,他们在开始睾酮治疗后中位6个月出现特发性骨坏死,作者研究了睾酮治疗与先前未诊断出的血栓形成倾向之间的相互作用。作者推测,开始睾酮治疗后发生骨坏死的患者比110名正常对照受试者或48名患有骨坏死但未接受睾酮治疗的患者更有可能患有血栓形成倾向。血栓形成倾向的指标包括因子V莱顿突变、凝血酶原、PAI-1基因突变、因子VIII、因子XI、抗心磷脂抗体免疫球蛋白G或免疫球蛋白M以及同型半胱氨酸值。在10例病例中,骨坏死发生在睾酮治疗开始后6个月或更短时间内,在所有16例病例中,中位发生时间为睾酮治疗6个月后。在这16例病例中,5例(31%)为因子V莱顿杂合子,而109名健康对照受试者中有2例(2%)(P=0.0003),48名患有骨坏死但未接受睾酮治疗的患者中有4例(P=0.04)。在这16例病例中,4例(25%)因子VIII水平高(>150%),而103名健康对照受试者中有7例(7%)(P=0.04),3例(19%)因子XI水平高(>150%),而101名健康对照受试者中有3例(3%)(P=0.03)。在16例骨坏死患者中,14例(88%)至少有1项(共测量8项)促凝血异常值,而110名健康对照受试者中有47例(43%)(P=0.0009)。在接受睾酮治疗时测量血清雌二醇水平的5名男性中,4名该水平较高(≥42.6 pg/mL)。当对患有血栓形成倾向的患者进行睾酮治疗时,他们发生骨坏死的风险会增加。

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