Rees D Aled, Udiawar Maneesh, Berlot Rok, Jones Derek K, O'Sullivan Michael J
Institute of Molecular and Experimental Medicine (D.A.R., M.U.), School of Medicine and Cardiff University Brain Research Imaging Centre (M.U., D.K.J., M.J.O.), School of Psychology, Cardiff University, Cardiff CF24 4HQ, United Kingdom; Department of Basic and Clinical Neuroscience (R.B., M.J.O.), Institute of Psychiatry Psychology and Neuroscience, King's College London, London SE5 9RX, United Kingdom; and Department of Neurology (R.B.), University Medical Centre Ljubljana, Zaloska cesta 2, 1000 Ljubljana, Slovenia.
J Clin Endocrinol Metab. 2016 Jan;101(1):314-23. doi: 10.1210/jc.2015-2318. Epub 2015 Nov 17.
Polycystic ovary syndrome (PCOS) is a disorder characterized by insulin resistance and hyperandrogenism, which leads to an increased risk of type 2 diabetes in later life. Androgens and insulin signaling affect brain function but little is known about brain structure and function in younger adults with PCOS.
To establish whether young women with PCOS display altered white matter microstructure and cognitive function. PATIENTS, INTERVENTIONS, AND MAIN OUTCOME MEASURES: Eighteen individuals with PCOS (age, 31 ± 6 y; body mass index [BMI] 30 ± 6 kg/m(2)) and 18 control subjects (age, 31 ± 7 y; BMI, 29 ± 6 kg/m(2)), matched for age, IQ, and BMI, underwent anthropometric and metabolic evaluation, diffusion tensor MRI, a technique especially sensitive to brain white matter structure, and cognitive assessment. Cognitive scores and white matter diffusion metrics were compared between groups. White matter microstructure was evaluated across the whole white matter skeleton using tract-based spatial statistics. Associations with metabolic indices were also evaluated.
PCOS was associated with a widespread reduction in axial diffusivity (diffusion along the main axis of white matter fibers) and increased tissue volume fraction (the proportion of volume filled by white or grey matter rather than cerebrospinal fluid) in the corpus callosum. Cognitive performance was reduced compared with controls (first principal component, t = 2.9, P = .007), reflecting subtle decrements across a broad range of cognitive tests, despite similar education and premorbid intelligence. In PCOS, there was a reversal of the relationship seen in controls between brain microstructure and both androgens and insulin resistance.
White matter microstructure is altered, and cognitive performance is compromised, in young adults with PCOS. These alterations in brain structure and function are independent of age, education and BMI. If reversible, these changes represent a potential target for treatment.
多囊卵巢综合征(PCOS)是一种以胰岛素抵抗和高雄激素血症为特征的疾病,这会导致日后患2型糖尿病的风险增加。雄激素和胰岛素信号传导会影响脑功能,但对于患有PCOS的年轻成年人的脑结构和功能了解甚少。
确定患有PCOS的年轻女性是否存在白质微观结构和认知功能的改变。患者、干预措施及主要观察指标:18例PCOS患者(年龄31±6岁;体重指数[BMI] 30±6kg/m²)和18例对照者(年龄31±7岁;BMI 29±6kg/m²),年龄、智商和BMI相匹配,接受人体测量和代谢评估、扩散张量磁共振成像(一种对脑白质结构特别敏感的技术)以及认知评估。比较两组之间的认知得分和白质扩散指标。使用基于纤维束的空间统计学方法在整个白质骨架上评估白质微观结构。还评估了与代谢指标的相关性。
PCOS与胼胝体中轴向扩散率(沿白质纤维主轴的扩散)广泛降低以及组织体积分数增加(白质或灰质而非脑脊液填充的体积比例)有关。与对照组相比,认知表现降低(第一主成分,t = 2.9,P = 0.007),尽管教育程度和病前智力相似,但反映出在广泛的认知测试中存在细微下降。在PCOS患者中,脑微观结构与雄激素和胰岛素抵抗之间的关系与对照组相反。
患有PCOS的年轻成年人白质微观结构发生改变,认知表现受损。这些脑结构和功能的改变与年龄、教育程度和BMI无关。如果这些变化是可逆的,那么它们代表了一个潜在的治疗靶点。