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左旋甲状腺素替代剂量与中枢性甲状腺功能减退症与原发性甲状腺功能减退症治疗评估的关系。

EVALUATION OF TREATMENT OF CENTRAL HYPOTHYROIDISM VERSUS PRIMARY HYPOTHYROIDISM IN RELATION TO LEVOTHYROXINE REPLACEMENT DOSE.

出版信息

Endocr Pract. 2019 Jul;25(7):663-668. doi: 10.4158/EP-2018-0533. Epub 2019 Mar 13.

DOI:10.4158/EP-2018-0533
PMID:30865544
Abstract

The aim of this study was to evaluate levothyroxine (LT4) replacement daily doses in patients with central hypothyroidism (CeH) and compare them with those adequate for patients with primary hypothyroidism (P-HYPO). We included 53 patients with CeH and 57 with P-HYPO, matched by sex, age, weight, and body mass index, in the period of 1 year. At the time of inclusion, all presented a stable and adequate dose of LT4 for at least 3 months, considering as adequate the dose associated with normal thyroid-stimulating hormone (TSH) levels and free thyroxine (T4) in P-HYPO patients, and free T4 levels in CeH patients. The absolute daily dose of LT4 differed significantly between the two groups, 103.0 ± 27.1 μg (CeH) and 89.3 ± 32.0 μg (P-HYPO) ( = .017), even after adjustment for age, gender, and free T4 ( = .04). The LT4 dose adjusted to weight was also higher after adjustment for age, gender and free T4 ( = .04), with an average of 1.3 ± 0.4 μg/kg (CeH) and 1.2 ± 0.4 μg/kg (P-HYPO). Sheehan syndrome patients had a lower absolute daily dose of LT4 ( = .001), and patients who underwent pituitary radiotherapy required higher doses ( = .008). There was no difference in the daily dose of LT4 according to other pituitary hormone deficiencies. The results reinforce the relevance of a careful individualization of LT4 replacement in CeH management and the need for new markers for proper LT4 replacement therapy in such cases. = body mass index; = central hypothyroidism; = growth hormone; = levothyroxine; = primary hypothyroidism; = triiodothyronine; = thyroxine; = thyroid-stimulating hormone.

摘要

本研究旨在评估中枢性甲状腺功能减退症(CeH)患者的左甲状腺素(LT4)替代剂量,并与原发性甲状腺功能减退症(P-HYPO)患者的替代剂量进行比较。我们纳入了 53 例 CeH 患者和 57 例 P-HYPO 患者,按照性别、年龄、体重和体重指数进行匹配,随访时间为 1 年。纳入时,所有患者均接受了至少 3 个月的稳定且剂量合适的 LT4 治疗,对于 P-HYPO 患者,合适剂量定义为与正常促甲状腺激素(TSH)水平和游离甲状腺素(T4)相关的剂量,而对于 CeH 患者,合适剂量定义为游离 T4 水平。两组患者的 LT4 日绝对剂量差异有统计学意义,分别为 103.0±27.1μg(CeH)和 89.3±32.0μg(P-HYPO)(=0.017),即使在校正年龄、性别和游离 T4 后差异仍有统计学意义(=0.04)。在校正年龄、性别和游离 T4 后,按体重调整的 LT4 剂量也较高(=0.04),平均为 1.3±0.4μg/kg(CeH)和 1.2±0.4μg/kg(P-HYPO)。席汉综合征患者的 LT4 日绝对剂量较低(=0.001),接受垂体放疗的患者需要更高的剂量(=0.008)。其他垂体激素缺乏与 LT4 日剂量无关。这些结果强调了在 CeH 管理中仔细个体化 LT4 替代治疗的重要性,以及在这种情况下需要新的标志物来正确进行 LT4 替代治疗。

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