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通过放射免疫测定法测得的血清促卵泡激素和促黄体生成素与垂体功能减退患者的性发育相关。

Serum follicular-stimulating hormone and luteinizing hormone as measured by radioimmunoassay correlated with sexual development in hypopituitary subjects.

作者信息

Penny R, Foley T P, Blizzard R M

出版信息

J Clin Invest. 1972 Jan;51(1):74-80. doi: 10.1172/JCI106799.

Abstract

Serum follicular-stimulating hormone (FSH) and luteinizing hormone (LH) as determined by radioimmunoassay, were correlated with sexual development in 29 patients with hypopituitarism (ages 14.2-29.9 yr).16 of 25 idiopathic hypopituitary patients (20 males and 5 females) exhibited some degree of sexual development. Stage III of sexual development or beyond was achieved by 12 of the 16. Of 13 patients with growth hormone (GH), adrenocortical-stimulating hormone (ACTH), and thyroid-stimulating hormone (TSH) deficiency, 8 did not develop beyond stage I. In contrast, five of six patients with GH deficiency without ACTH or TSH deficiency developed to stage III of sexual development or beyond. The mean (+/-sd) serum LH concentration while in stage I (4.3 +/-0.9 mIU/ml) of eight patients (seven males and one female) who developed beyond stage I was significantly (P < 0.005) greater than the mean serum LH concentration (2.3 +/-0.9 mIU/ml) in nine patients (seven males and two females) who had not developed beyond stage I. Mean serum FSH concentrations were not different. Three of four males with organic hypopituitarism did not develop beyond stage I of sexual development. Serum FSH and LH concentrations in the idiopathic and organic hypopituitary patients were more compatible with stage of sexual development than with age. A serum LH concentration below the range of normal for stage I of sexual development in a prepubertal patient suggests that the patient will remain sexually infantile as an adult.

摘要

通过放射免疫测定法测定的血清促卵泡激素(FSH)和促黄体生成素(LH),与29例垂体功能减退患者(年龄14.2 - 29.9岁)的性发育情况相关。25例特发性垂体功能减退患者(20例男性和5例女性)中有16例表现出一定程度的性发育。16例患者中有12例达到了性发育的III期或更高级别。在13例生长激素(GH)、促肾上腺皮质激素(ACTH)和促甲状腺激素(TSH)缺乏的患者中,8例未超过I期发育。相比之下,6例无ACTH或TSH缺乏的GH缺乏患者中有5例发育到了性发育的III期或更高级别。8例(7例男性和1例女性)发育超过I期的患者在I期时的平均(±标准差)血清LH浓度(4.3±0.9 mIU/ml)显著高于(P<0.005)9例(7例男性和2例女性)未超过I期发育患者的平均血清LH浓度(2.3±0.9 mIU/ml)。平均血清FSH浓度无差异。4例器质性垂体功能减退男性患者中有3例未超过性发育的I期。特发性和器质性垂体功能减退患者的血清FSH和LH浓度与性发育阶段的相关性比与年龄的相关性更强。青春期前患者血清LH浓度低于性发育I期的正常范围表明该患者成年后将保持性幼稚状态。

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本文引用的文献

1
Radioimmunoassay for human luteinizing hormone.人促黄体生成素的放射免疫测定法。
Proc Soc Exp Biol Med. 1967 Aug-Sep;125(4):1130-3. doi: 10.3181/00379727-125-32295.
2
Radioimmunoassay for human follicle stimulating hormone.人促卵泡激素放射免疫测定法
J Clin Endocrinol Metab. 1967 Mar;27(3):444-7. doi: 10.1210/jcem-27-3-444.
4
Radioimmunoassay for human follicle-stimulating hormone.人促卵泡激素的放射免疫测定法
J Clin Endocrinol Metab. 1967 Feb;27(2):295-9. doi: 10.1210/jcem-27-2-295.
7
Radioimmunoassay for human luteinizing hormone.人促黄体生成素放射免疫测定法
Metabolism. 1966 Apr;15(4):287-9. doi: 10.1016/0026-0495(66)90142-9.
10
Radioimmunoassay of human follicle stimulating and luteinizing hormones in plasma.
J Clin Endocrinol Metab. 1968 Apr;28(4):519-34. doi: 10.1210/jcem-28-4-519.

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