Neuropsychiatric Institute, Euroa Centre, Prince of Wales Hospital, Randwick, NSW, Australia.
Centre for Healthy Brain Ageing, (CHeBA), School of Psychiatry, University of New South Wales (UNSW Sydney), Sydney, NSW, Australia.
Brain Imaging Behav. 2018 Jun;12(3):860-869. doi: 10.1007/s11682-017-9747-2.
Incidental findings on structural cerebral magnetic resonance imaging (MRI) are common in healthy subjects, and the prevalence increases with age. There is a paucity of data regarding incidental cerebral findings in twins. We examined brain MRI data acquired from community-dwelling older twins to determine the prevalence and concordance of incidental cerebral findings, as well as the associated clinical implications. Participants (n = 400) were drawn from the Older Australian Twins Study. T1-weighted and T2-weighted fluid-attenuated inversion recovery (FLAIR) cerebral MRI scans were systematically reviewed by a trained, blinded clinician. Incidental findings were recorded according to pre-determined categories, and the diagnosis confirmed by an experienced neuroradiologist. Periventricular and deep white matter hyperintensities (WMH) were scored visually. WMH heritability was calculated for those with the twin pair included in the study (n = 320 individuals; monozygotic (MZ) = 92 twin pairs, dizygotic (DZ) = 68 twin pairs). Excluding infarcts and WMH, a total of 47 (11.75%) incidental abnormalities were detected. The most common findings were hyperostosis frontalis interna (8 participants; 2%), meningiomas, (6 participants; 1.5%), and intracranial lipomas (5 participants; 1.25%). Only 3% of participants were referred for follow-up. Four twin pairs, all monozygotic, had lesions concordant with their twin. Periventricular WMH was moderately heritable (0.61, CI 0.43-0.75, p = 7.21E-08) and deep WMH highly heritable (0.80, CI 0.66-0.88, p = 1.76E-13). As in the general population, incidental findings on cerebral MRI in older twins are common, although concordance rates are low. Such findings can alter the clinical outcome of participants, and should be anticipated by researchers when designing trials involving cerebral imaging.
结构磁共振成像(MRI)的偶然发现常见于健康受试者,且其发生率随年龄增长而增加。双胞胎的脑部偶然发现的数据很少。我们检查了从社区居住的老年双胞胎中获取的脑 MRI 数据,以确定偶然脑部发现的发生率和一致性,以及相关的临床意义。参与者(n=400)取自老年澳大利亚双胞胎研究。由经过培训的、盲法临床医生系统地审查 T1 加权和 T2 加权液体衰减反转恢复(FLAIR)脑 MRI 扫描。根据预先确定的类别记录偶然发现,并由经验丰富的神经放射学家确认诊断。脑室周围和深部白质高信号(WMH)通过视觉评分。对于包括在研究中的双胞胎对(n=320 人;同卵(MZ)=92 对双胞胎,异卵(DZ)=68 对双胞胎),计算 WMH 的遗传性。排除梗死和 WMH 后,共发现 47 例(11.75%)偶然异常。最常见的发现是额骨内骨肥厚(8 例;2%)、脑膜瘤(6 例;1.5%)和颅内脂肪瘤(5 例;1.25%)。只有 3%的参与者被转介进行随访。有 4 对双胞胎,均为同卵,其病变与其双胞胎一致。脑室周围 WMH 具有中度遗传性(0.61,CI 0.43-0.75,p=7.21E-08),深部 WMH 具有高度遗传性(0.80,CI 0.66-0.88,p=1.76E-13)。与一般人群一样,老年双胞胎脑 MRI 的偶然发现很常见,尽管一致性率较低。这些发现可能改变参与者的临床结果,研究人员在设计涉及脑部成像的试验时应有所预期。