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家族性甲状腺素结合球蛋白缺乏症患者血清促甲状腺激素对促甲状腺激素释放激素的反应及游离甲状腺激素指标

Serum thyrotropin response to thyrotropin-releasing hormone and free thyroid hormone indices in patients with familiar thyroxine-binding globulin deficiency.

作者信息

Konno N

出版信息

Endocrinol Jpn. 1976 Aug;23(4):313-7.

PMID:828576
Abstract

The response in serum thyrotropin (TSH) to synthetic thyrotropin-releasing hormone (TRH) as well as serum free thyroxine index (FT4I) and free triiodothyronine index (FT3I) was investigated in six patients with familial thyroxine-binding-globulin (TBG) deficiency. The total serum thyroxine (T4) and triiodothyronine (T3) concentrations were significantly decreased, compared with those of normal subjects (3,4 +/- 0.9 microng/dl, mean +/- S.D. vs. 9.0 +/- 1.5 microng/dl, p less than 0.01 and 87 +/- ng/dl vs. 153 +/- 37 ng/dl, p less than 0.01, respectively). FT4I was lower than the normal range in all but one (5.3 +/- 1.5 vs. 8.9 +/- 1.6, p less than 0.01), whereas FT3I was all in the normal range and of no significant difference from the normal control (132 +/- 22 vs 148 +/- 25). Serum TSH concentrations in TBG deficiency were all in the normal range (1.0-4.2 micronM/ml) and the maximum TSH increments following TRH 500 microng iv were 8.9 +/- 2.0 micronU/ml and of no significant difference from the normal control (10.2 +/- 4.5 micronU/ml). These results indicate that the euthyroid state in familial TBG deficiency is more clearly defined by TRH-test and the normal response to TRH in familial TBG deficiency is presumably under the control of the serum free T3 level rather than the serum free T4 level.

摘要

对6例家族性甲状腺素结合球蛋白(TBG)缺乏症患者,研究了血清促甲状腺激素(TSH)对合成促甲状腺激素释放激素(TRH)的反应,以及血清游离甲状腺素指数(FT4I)和游离三碘甲状腺原氨酸指数(FT3I)。与正常受试者相比,血清总甲状腺素(T4)和三碘甲状腺原氨酸(T3)浓度显著降低(分别为3.4±0.9μg/dl,均值±标准差,正常受试者为9.0±1.5μg/dl,p<0.01;87±ng/dl,正常受试者为153±37ng/dl,p<0.01)。除1例患者外,其余患者的FT4I均低于正常范围(5.3±1.5 vs. 8.9±1.6,p<0.01),而FT3I均在正常范围内,与正常对照组无显著差异(132±22 vs 148±25)。TBG缺乏症患者的血清TSH浓度均在正常范围内(1.0 - 4.2μM/ml),静脉注射500μg TRH后TSH的最大增加值为8.9±2.0μU/ml,与正常对照组无显著差异(10.2±4.5μU/ml)。这些结果表明,家族性TBG缺乏症中的甲状腺功能正常状态通过TRH试验能更清晰地界定,家族性TBG缺乏症中对TRH的正常反应可能受血清游离T3水平而非血清游离T4水平的控制。

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