首页> 外文期刊>European journal of human genetics: EJHG >Preliminary evidence of a noncausal association between the X-chromosome inactivation pattern and thyroid autoimmunity: a twin study.
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Preliminary evidence of a noncausal association between the X-chromosome inactivation pattern and thyroid autoimmunity: a twin study.

机译:X染色体灭活模式与甲状腺自身免疫性之间无因果关系的初步证据:一项孪生研究。

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An increased frequency of skewed X-chromosome inactivation (XCI) is found in clinically overt autoimmune thyroid disease (AITD) compared with controls. Whether skewed XCI is involved in the pathogenesis of autoantibodies to thyroid peroxidase (TPOAb) in euthyroid subjects is unknown. To examine the impact of XCI on the serum concentration of TPOAb, we studied whether within-cohort and within-twin-pair differences in XCI are associated with differences in serum concentrations of TPOAb. A total of 318 euthyroid female twin individuals distributed in 159 pairs were investigated. XCI was determined by PCR analysis of a polymorphic CAG repeat in the first exon of the androgen receptor gene. TPOAb concentrations were measured using a solid-phase time-resolved fluoroimmunometric assay. Overall (within cohort), there was a significant association between XCI and serum concentrations of TPOAb; regression coefficient (beta)=1.45 (95% confidence interval, 0.52-2.38), P=0.003. The association remained significant in the within-pair analysis; beta=1.74 (0.79-2.69), P<0.001. The relationship was nonsignificant within the 82 monozygotic pairs (beta=0.57 (-0.78-1.92), P=0.405), whereas the association was significant in the 77 dizygotic pairs (beta=2.17 (0.81-3.53), P=0.002). This preliminary finding of a significant association between TPOAb concentrations and XCI within cohort and within dizygotic but not within monozygotic twin pairs may indicate that XCI per se does not have a major role in the pathogenesis of TPOAb. More likely, XCI and TPOAb are influenced by shared genetic determinants.
机译:与对照组相比,临床上明显的自身免疫性甲状腺疾病(AITD)发现偏斜X染色体失活(XCI)的频率增加。偏向XCI是否参与正常甲状腺疾病患者甲状腺过氧化物酶(TPOAb)自身抗体的发病机制。为了检查XCI对TPOAb血清浓度的影响,我们研究了XCI的队列内和双胞胎对差异是否与TPOAb血清浓度差异相关。共调查了318对甲状腺雌性双胎个体,分布在159对中。通过对雄激素受体基因的第一个外显子中的多态性CAG重复进行PCR分析来确定XCI。使用固相时间分辨荧光免疫测定法测量TPOAb浓度。总体而言(在队列内),XCI与血清TPOAb浓度之间存在显着相关性。回归系数β= 1.45(95%置信区间,0.52-2.38),P = 0.003。该关联在配对内分析中仍然很重要; β= 1.74(0.79-2.69),P <0.001。该关系在82个单合子对中无显着性(β= 0.57(-0.78-1.92),P = 0.405),而在77个双合子对中相关性显着(β= 2.17(0.81-3.53),P = 0.002)。队列中和同卵双生子对内而不是同卵双生子对内TPOAb浓度与XCI之间存在显着关联的初步发现可能表明XCI本身在TPOAb的发病机理中没有主要作用。 XCI和TPOAb更有可能受到共享遗传决定因素的影响。

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