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Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course

机译:土耳其短暂性先天性甲状腺功能减退症:频率和自然过程的分析

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摘要

>Objective: Prevalence of congenital hypothyroidism (CH) in Turkey at birth was reported to be as high as 1:650 in 2008-2010. Incidence rates of permanent and transient CH separately are unknown due to lack of follow-up data. We aimed to evaluate the impact of transient hypothyroidism on increasing incidence of CH and to determine the natural course and the clinical, biochemical, and imaging characteristics of transient CH.>Methods: Baseline and follow-up data of the infants with CH detected at screening in six provinces in the Black Sea Region were analyzed retrospectively during a time period covering the years 2008-2010.>Results: Among 138 cases (48% female), 16 (12%) showed transient hyperthyrotropinemia which resolved without intervention. Of the treated 122 cases, 63 (52%) had transient CH. While its frequency was 35% in 2008, it increased to 56% in 2009-2010, following a lowering of the thyroid stimulating hormone cutoff value. The frequency was higher in inland provinces than in coast (67% vs. 43%; p=0.01).Clinical characteristics of permanent and transient cases were similar except female-to-male sex ratios (1.5:1 vs. 0.6:1; p=0.02). L-thyroxine was discontinued in 70% of transient cases before 3 years of age at a median age of 19 (2-36) months. The only indication for early discontinuation of treatment was a low L-thyroxine dose, which was 1.25±0.27 µg/kg/day at withdrawal time.>Conclusion: Our regional follow-up data showed that more than half of newborns with primary CH had transient thyroid dysfunction. In the majority of cases, discrimination between transient and permanent CH can be made before age 3 years, as indicated by cessation of L-thyroxine treatment.
机译:>目的:据报道,在土耳其出生时,先天性甲状腺功能低下症(CH)的患病率在2008-2010年高达1:650。由于缺乏随访数据,永久性和短暂性CH的发生率分别未知。我们旨在评估短暂性甲状腺功能减退症对CH发病率增加的影响,并确定其自然病程以及瞬时CH的临床,生化和影像学特征。>方法:回顾性分析了2008-2010年期间在黑海地区六个省进行筛查时发现的CH婴儿。>结果:在138例(女性48%)中,有16例(12%) )显示短暂性甲状腺素过高症,无需干预即可解决。在治疗的122例病例中,有63例(52%)患有短暂性CH。虽然其频率在2008年为35%,但由于降低了甲状腺刺激激素的临界值,在2009-2010年增加到56%。内陆省份的发病率高于沿海省份(67%比43%; p = 0.01)。永久和短暂病例的临床特征相似,除了男女比例(1.5:1 vs. 0.6:1; p = 0.02)。 70%的短暂性病例在3岁之前停用L-甲状腺素,中位年龄为19(2-36)个月。早期停止治疗的唯一迹象是低的L-甲状腺素剂量,停药时为1.25±0.27 µg / kg /天。>结论:我们的区域随访数据显示,一半以上的原发性CH新生儿有短暂的甲状腺功能障碍。在大多数情况下,如停止使用L-甲状腺素表明,可以在3岁​​之前对暂时性和永久性CH进行区分。

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