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日本辅助生殖技术后的先天性甲状腺功能减退症:2005 - 2009年多胎与单胎的比较

Congenital hypothyroidism after assisted reproductive technology in Japan: comparison between multiples and singletons, 2005-2009.

作者信息

Ooki Syuichi

机构信息

Department of Health Science, Ishikawa Prefectural Nursing University, 1-1, Gakuendai, Kahoku, Ishikawa, 929-1210, Japan.

出版信息

Int J Pediatr Endocrinol. 2013 Feb 12;2013(1):5. doi: 10.1186/1687-9856-2013-5.

Abstract

BACKGROUND

The relationship between congenital hypothyroidism (CH) and multiple pregnancy has not been fully studied in Japan.

METHODS

Complete nationwide data of assisted reproductive technology (ART) in Japan from 2005 to 2009 presented by the Japan Society of Obstetrics and Gynecology, which include information on CH and birth defects were used for analyses. Diseases were reclassified according to the International Classification of Diseases, tenth edition (ICD-10, 2003 version). The relative risk (RR) and 95% confidence interval (CI) of the incidence rate for CH was calculated with singletons as the reference group. Additional birth defects with CH were examined. The probandwise concordance rate of multiples and recurrence risk ratio were calculated.

RESULTS

There were 18 patients with CH, consisting of 12 singletons and 6 multiples. The incidence rates of CH per 1,000 live births in singletons and multiples are 0.14 (=12/87,145) and 0.31 (=6/19,533), respectively. The incidence rate was more than twofold higher in multiple births than in singleton births, but the difference was not statistically significant (RR=2.2, 95% CI 0.8-5.9). Additional birth defects were present in three patients with CH (17%=3/18). The multiples were affected by other birth defects more frequently (33%=2/6) than the singletons (8%=1/12). The six multiple-births patients were derived from one concordant twin pair, which consisted of two twin patients; three discordant twin pairs, which consisted of three twin patients; and one discordant triplets set, which consisted of one triplet patient. Thus, the probandwise concordance rate was 33.3% (=2/(2+4)). The estimated recurrence risk ratio was 1976 (for the total ART population) or 609 (for the Japanese general population).

CONCLUSIONS

CH was more frequent in multiples compared to singletons. A higher percentage of additional birth defects was also observed in multiples compared to singletons. The familial aggregation of CH was suggested.

摘要

背景

在日本,先天性甲状腺功能减退症(CH)与多胎妊娠之间的关系尚未得到充分研究。

方法

使用日本妇产科学会提供的2005年至2009年日本全国辅助生殖技术(ART)的完整数据进行分析,这些数据包括CH和出生缺陷的信息。疾病根据国际疾病分类第十版(ICD - 10,2003年版)重新分类。以单胎妊娠作为参照组,计算CH发病率的相对风险(RR)和95%置信区间(CI)。对伴有CH的其他出生缺陷进行检查。计算多胎妊娠的先证者一致率和复发风险比。

结果

有18例CH患者,其中单胎12例,多胎6例。单胎和多胎中每1000例活产儿的CH发病率分别为0.14(=12/87,145)和0.31(=6/19,533)。多胎妊娠的发病率比单胎妊娠高出两倍多,但差异无统计学意义(RR = 2.2,95% CI 0.8 - 5.9)。18例CH患者中有3例存在其他出生缺陷(17% = 3/18)。多胎妊娠受其他出生缺陷影响的频率(33% = 2/6)高于单胎妊娠(8% = 1/12)。6例多胎妊娠患者来自1对一致的双胞胎(由2名双胞胎患者组成)、3对不一致的双胞胎(由3名双胞胎患者组成)和1组不一致的三胞胎(由1名三胞胎患者组成)。因此,先证者一致率为33.3%(=2/(2 + 4))。估计的复发风险比为1976(针对整个ART人群)或609(针对日本普通人群)。

结论

与单胎妊娠相比,多胎妊娠中CH更为常见。与单胎妊娠相比,多胎妊娠中其他出生缺陷的比例也更高。提示CH存在家族聚集性。

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