Under-recognised neurocognitive deficits in adults and adolescents with tuberous sclerosis complex.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Journal of Medical Genetics Pub Date : 2025-01-19 DOI:10.1136/jmg-2024-110388
Mélissa Boisclair, Laury-Anne Blondeau, Florence Bouchard, Rose-Marie Drouin-Engler, Jimmy Li, Samuel Bertrand, Fayçal Zine-Eddine, Laurent Létourneau-Guillon, Catherine Larochelle, Philippe Major, Olivier Boucher, Mark R Keezer
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Abstract

Background: Tuberous sclerosis complex (TSC) is a genetic disease characterised by the growth of benign tumours. The Tuberous sclerosis Associated Neuropsychiatric Disorders (TAND) Checklist is used to identify patient-reported neurocognitive deficits. Patients may, however, under-recognise mild cognitive impairment. We aimed to determine the frequency of abnormal scores on three objective tests of cognitive function in people with and without diagnosed intellectual disability and examine associations between scores on these tests with self-reported TAND Checklist symptoms.

Methods: We conducted a cross-sectional study where people with TSC (PwTSC; n=46) completed the TAND Checklist and three cognitive tests: Symbol Digit Modalities Test (SDMT), Montreal Cognitive Assessment test and Trail Making Test-Parts A and B. We examined associations between cognitive test scores and the TAND Checklist using Pearson's correlations (95% CI). Receiver operating characteristics (ROC) curves were plotted to determine the screening accuracy of each measure in identifying physician-diagnosed neurocognitive disorders.

Results: There were minimal correlations between the cognitive test scores and the TAND Checklist. More than 20% of PwTSC reported no cognitive issues on the TAND Checklist but had abnormal performance on at least one cognitive test. The ROC curves demonstrated similar results, with areas under the curve of 0.93 (95% CI 0.79 to 1.00) for the SDMT but only 0.70 (95% CI 0.45 to 0.95) for the TAND Checklist.

Conclusion: Objective tests of cognitive function are useful in identifying unrecognised neurocognitive deficits in PwTSC. Deficits likely have multifactorial origins, including undiagnosed intellectual disability and the impact of chronic epilepsy.

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成人和青少年结节性硬化症患者未被认识到的神经认知缺陷。
背景:结节性硬化症(TSC)是一种以良性肿瘤生长为特征的遗传性疾病。结节性硬化症相关神经精神障碍(TAND)检查表用于识别患者报告的神经认知缺陷。然而,患者可能对轻度认知障碍认识不足。我们的目的是确定有和没有被诊断为智力残疾的人在三项认知功能客观测试中异常得分的频率,并检查这些测试得分与自我报告的TAND检查表症状之间的关系。方法:我们进行了一项横断面研究,其中患有TSC (PwTSC;n=46)完成了TAND清单和三个认知测试:符号数字模态测试(SDMT),蒙特利尔认知评估测试和轨迹制作测试-部分A和b。我们使用Pearson's相关性(95% CI)检验了认知测试分数与TAND清单之间的关联。绘制受试者工作特征(ROC)曲线,以确定识别医生诊断的神经认知障碍的每项测量的筛查准确性。结果:认知测验成绩与TAND量表之间的相关性很小。超过20%的PwTSC报告在TAND检查表上没有认知问题,但在至少一项认知测试中表现异常。ROC曲线显示了类似的结果,SDMT的曲线下面积为0.93 (95% CI 0.79至1.00),而TAND Checklist的曲线下面积仅为0.70 (95% CI 0.45至0.95)。结论:客观的认知功能测试有助于发现PwTSC未被识别的神经认知缺陷。缺陷可能有多因素的原因,包括未确诊的智力残疾和慢性癫痫的影响。
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来源期刊
Journal of Medical Genetics
Journal of Medical Genetics 医学-遗传学
CiteScore
7.60
自引率
2.50%
发文量
92
审稿时长
4-8 weeks
期刊介绍: Journal of Medical Genetics is a leading international peer-reviewed journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles cover the molecular basis of human disease including germline cancer genetics, clinical manifestations of genetic disorders, applications of molecular genetics to medical practice and the systematic evaluation of such applications worldwide.
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