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儿童和青少年期的内分泌紊乱。儿童和青少年亚临床甲状腺功能减退症的自然病程和替代治疗的潜在影响:综述。

Endocrine disorders in childhood and adolescence. Natural history of subclinical hypothyroidism in children and adolescents and potential effects of replacement therapy: a review.

机构信息

Department of Health Sciences, Università del Piemonte Orientale, Novara, Italy.

出版信息

Eur J Endocrinol. 2012 Dec 10;168(1):R1-R11. doi: 10.1530/EJE-12-0656. Print 2013 Jan.

Abstract

OBJECTIVE

Subclinical hypothyroidism (SH) is quite common in children and adolescents. The natural history of this condition and the potential effects of replacement therapy need to be known to properly manage SH. The aim of this review is to analyze: i) the spontaneous evolution of SH, in terms of the rate of reversion to euthyroidism, the persistence of SH, or the progression to over hypothyroidism; and ii) the effects of replacement therapy, with respect to auxological data, thyroid volume, and neuropsychological functions.

METHODS

We systematically searched PubMed, Cochrane, and EMBASE (1990-2012) and identified 39 potentially relevant articles of which only 15 articles were suitable to be included.

RESULTS AND CONCLUSIONS

SH in children is a remitting process with a low risk of evolution toward overt hypothyroidism. Most of the subjects reverted to euthyroidism or remained SH, with a rate of evolution toward overt hypothyroidism ranging between 0 and 28.8%, being 50% in only one study (nine articles). The initial presence of goiter and elevated thyroglobulin antibodies, the presence of celiac disease, and a progressive increase in thyroperoxidase antibodies and TSH value predict a progression toward overt hypothyroidism. Replacement therapy is not justified in children with SH but with TSH 5-10 mIU/l, no goiter, and negative antithyroid antibodies. An increased growth velocity was observed in children treated with levothyroxine (l-T(4); two articles). l-T(4) reduced thyroid volume in 25-100% of children with SH and autoimmune thyroiditis (two studies). No effects on neuropsychological functions (one study) and posttreatment evolution of SH (one study) were reported.

摘要

目的

亚临床甲状腺功能减退症(SH)在儿童和青少年中较为常见。为了正确管理 SH,需要了解这种疾病的自然病史和替代治疗的潜在影响。本综述的目的是分析:i)SH 的自发演变,包括恢复正常甲状腺功能的比率、SH 的持续存在或发展为过度甲状腺功能减退的情况;ii)替代治疗的效果,包括生长数据、甲状腺体积和神经心理学功能。

方法

我们系统地检索了 PubMed、Cochrane 和 EMBASE(1990-2012 年),并确定了 39 篇可能相关的文章,其中只有 15 篇适合纳入。

结果和结论

儿童 SH 是一个缓解过程,向显性甲状腺功能减退症发展的风险较低。大多数患者恢复到正常甲状腺功能或仍处于 SH 状态,向显性甲状腺功能减退症发展的比率在 0 到 28.8%之间,只有一项研究(9 篇文章)中为 50%。初始存在甲状腺肿和升高的甲状腺球蛋白抗体、乳糜泻的存在以及甲状腺过氧化物酶抗体和 TSH 值的逐渐增加,预测向显性甲状腺功能减退症的进展。SH 患儿 TSH 为 5-10mIU/L、无甲状腺肿和阴性抗甲状腺抗体时,无需进行替代治疗。在接受左甲状腺素(l-T4)治疗的儿童中观察到生长速度加快(两项研究)。l-T4 可使 25-100%的 SH 和自身免疫性甲状腺炎患儿的甲状腺体积缩小(两项研究)。替代治疗对神经心理学功能(一项研究)和治疗后 SH 的演变(一项研究)无影响。

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