Edan G, Massart C, Hody B, Poirier J Y, Lé Reun M, Hespel J P, Leclech G, Simon M
Clinique Médicale B, Hôpital Sud, Rennes, France.
BMJ. 1989 Feb 11;298(6670):359-61. doi: 10.1136/bmj.298.6670.359.
To determine the optimal duration of antithyroid drug treatment by monitoring serum thyroid stimulating antibody values in patients with Graves' disease.
Prospective longitudinal trial of patients with Graves' disease followed up for 24 months after withdrawal of treatment.
Tertiary referral centre.
A total of 64 consecutive patients with untreated Graves' disease, eight of whom were subsequently excluded. Fifty six patients completed the study.
All patients were treated initially with carbimazole 40 mg, then with decreasing doses that maintained a euthyroid state. Treatment was scheduled to continue for 18 months but was withdrawn earlier if serum thyroid stimulating antibody became undetectable.
Serum values of thyroid stimulating antibody (assayed by stimulation of human thyroid cells in vitro) and thyroid hormones and thyroid state every three months during treatment and afterwards every six months for 24 months.
In 44 patients serum thyroid stimulating antibody became undetectable during treatment and treatment was withdrawn (median duration of treatment nine months, range 3-18 months). In 12 patients the antibody could be detected during 18 months of treatment. Among the first group of 44 patients initial values of the antibody before treatment were significantly lower than in the second group of 12 patients (median 225% (range 138-1236%) v 570% (250-1480%), p less than 0.001); the incidence of relapse was also lower (41% v 92%, p less than 0.001); and among those who did relapse the disease free interval after treatment was longer (median 12 months v 1 month, p less than 0.001). Moreover, the initial median serum values of thyroid stimulating antibodies were not related to the occurrence of relapse or remission as these did not differ between patients who did and did not have a relapse (median 267% (range 139-1480%) v 220% (range 138-1236%).
Monitoring of serum thyroid stimulating antibody was a good guide to the duration of treatment as it allowed the treatment period to be considerably shortened in a large group of patients with no loss of efficiency.
通过监测格雷夫斯病患者血清促甲状腺素抗体值来确定抗甲状腺药物治疗的最佳疗程。
对格雷夫斯病患者进行前瞻性纵向试验,治疗停药后随访24个月。
三级转诊中心。
共有64例未经治疗的格雷夫斯病患者,其中8例随后被排除。56例患者完成了研究。
所有患者最初均接受40毫克卡比马唑治疗,然后逐渐减量以维持甲状腺功能正常状态。治疗计划持续18个月,但如果血清促甲状腺素抗体检测不到则提前停药。
治疗期间每三个月以及之后24个月每六个月检测血清促甲状腺素抗体(通过体外刺激人甲状腺细胞测定)、甲状腺激素及甲状腺状态的值。
44例患者在治疗期间血清促甲状腺素抗体检测不到,治疗停药(治疗中位疗程9个月,范围3 - 18个月)。12例患者在18个月治疗期间抗体仍可检测到。在第一组44例患者中,治疗前抗体初始值显著低于第二组12例患者(中位值225%(范围138 - 1236%)对570%(250 - 1480%),p<0.001);复发率也较低(41%对92%,p<0.001);在复发患者中,治疗后无病间期更长(中位值12个月对1个月,p<0.001)。此外,促甲状腺素抗体的初始血清中位值与复发或缓解的发生无关,因为复发患者和未复发患者之间并无差异(中位值267%(范围139 - 1480%)对220%(范围138 - 1236%))。
监测血清促甲状腺素抗体对治疗疗程是一个很好的指导,因为它能在不降低疗效的情况下,使一大组患者的治疗期大幅缩短。