Snijders G, de Witte L, Mesman E, Kemner S, Vonk R, Brouwer R, Nolen W A, Drexhage H A, Hillegers M H J
Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, P.O. Box 85500, Heidelberglaan 100, 3508 GA, Utrecht, The Netherlands.
Department of Psychiatry, Reinier van Arkel, Den Bosch, The Netherlands.
Int J Bipolar Disord. 2017 Dec;5(1):1. doi: 10.1186/s40345-017-0070-z. Epub 2017 Jan 20.
Previous studies of our group among bipolar offspring and bipolar twins showed significant higher prevalence's and levels of antithyroid peroxidase antibodies (TPO-Abs) in offspring and co-twins (without a mood disorder) compared to controls, suggesting that TPO-Abs might be considered as vulnerability factor (trait marker) for BD development.
Here we elucidate, in the same cohorts, but now after 12- and 6-year follow-up, whether TPO-abs should be considered as a 'trait' marker for BD. The present study aims to investigate whether TPO-Abs (1) are stable over time, (2) are associated with lithium-exposure, (3) share a common genetic background with BD and are related to psychopathology.
In bipolar offspring and twins, the prevalence of TPO-Abs is stable over time (r = .72 p < .001 resp. r = .82, p < .001) and not associated with lithium use. At follow-up, an increased prevalence of TPO-abs was again observed in bipolar offspring (10,4% versus 4%) and higher TPO-abs titers were still present in co-twins of bipolar cases compared to control twins [mean 1.06 IU/ml (SD .82) versus mean .82 IU/ml (SD .67)], although statistical significance was lost.
Although our results show a trend toward an increased inherited risk of the co-occurrence of BD and thyroid autoimmunity, large-scale studies can only draw final conclusions. Nationwide epidemiological and GWAS studies reach such numbers and support the view of a possible common (autoimmune) etiology of severe mood disorders and chronic recurrent infections and autoimmunity, including thyroid autoimmunity.
我们团队之前对双相情感障碍患者的后代及双生子进行的研究表明,与对照组相比,后代及双生子(无心境障碍)中抗甲状腺过氧化物酶抗体(TPO-Abs)的患病率及水平显著更高,这表明TPO-Abs可能被视为双相情感障碍发病的易患因素(特质标记)。
在此,我们在同一队列中,但在12年和6年随访之后,阐明TPO-Abs是否应被视为双相情感障碍的“特质”标记。本研究旨在调查TPO-Abs:(1)随时间是否稳定;(2)是否与锂暴露相关;(3)是否与双相情感障碍共享共同的遗传背景并与精神病理学相关。
在双相情感障碍后代及双生子中,TPO-Abs的患病率随时间稳定(分别为r = 0.72,p < 0.001;r = 0.82,p < 0.001),且与锂的使用无关。随访时,双相情感障碍后代中TPO-Abs的患病率再次升高(10.4%对4%),与对照双生子相比,双相情感障碍患者的双生子中TPO-Abs滴度仍更高[平均1.06 IU/ml(标准差0.82)对平均0.82 IU/ml(标准差0.67)],尽管失去了统计学意义。
尽管我们的结果显示双相情感障碍与甲状腺自身免疫共病的遗传风险增加有一定趋势,但大规模研究才能得出最终结论。全国性的流行病学和全基因组关联研究达到了这样的样本量,并支持了严重心境障碍与慢性复发性感染及自身免疫(包括甲状腺自身免疫)可能存在共同(自身免疫性)病因的观点。