corpus callosum

Callosum Corpus Callosum
  • 文章类型: Journal Article
    可以观察到各种疾病继发的RESLES(可逆性脾病变综合征),淀粉样蛋白内水肿可能在SCC(call体脾)的发病机理中起关键作用。一些研究表明,缺氧缺血性脑病可能是SCC病变的危险因素。然而,高海拔环境对SCC的潜在影响,尤其是在慢性暴露期间,保持模糊。
    我们的研究包括19名在高海拔地区符合RESLES诊断标准的患者。包括十名患有RESLES的低海拔患者作为对照。所有参与者都接受了两次MRI(磁共振成像)扫描。常规血液检查,肝脏,肾脏和甲状腺功能,凝血功能,在住院期间和出院前检测电解质和维生素.此外,患者于2023年5月获得随访.
    高海拔的低氧环境可能会增加RESLES的风险。两组均表现出不同的临床症状。高海拔患者的CRP水平明显高于低海拔患者。高海拔患者的病变大小与SaO2水平呈正相关。然而,低海拔的患者病变大小与几种炎症标志物呈正相关趋势(WBC,NEU和CRP)。所有患者的预后良好,可能不受醋酸泼尼松的影响。
    高海拔地区的低氧环境可能在RESLES的病因中起作用。此外,RESLES是一种可逆的疾病,糖皮质激素的给药对于其治疗可能是不必要的。
    UNASSIGNED: RESLES (Reversible splenial lesion syndrome) can be observed secondary to various diseases, and intramyelinic edema may play a crucial role in the pathogenesis of SCC (Splenium of the corpus callosum). Some studies have suggested that hypoxic-ischaemic encephalopathy may constitute a risk factor for SCC lesions. However, the potential impact of high-altitude environments on SCC, especially during chronic exposure, remain obscure.
    UNASSIGNED: Our study included 19 patients who satisfied the diagnostic criteria of RESLES at high altitudes. Ten low-altitude patients with RESLES were included as controls. All participants received MRI (Magnetic resonance imaging) scans twice. Routine blood tests, liver, kidney and thyroid function, coagulation function, electrolytes and vitamins were detected during hospitalization and before discharge. In addition, the patients were followed up in May 2023.
    UNASSIGNED: Hypoxic environments at high altitudes may increase the risk of RESLES. The two groups showed different clinical symptoms. High-altitude patients had significantly higher CRP levels than low-altitude patients. The lesion size in high-altitude patients showed a positive correlation with SaO2 levels. However, the patients at low altitudes had positive correlation trends between lesion size and several inflammatory markers (WBC, NEU and CRP). All patients had a benign prognosis that may not be affected by the use of prednisone acetate.
    UNASSIGNED: Hypoxic environments at high altitudes may play a role in the aetiology of RESLES. Additionally, RESLES is a reversible disease and the administration of glucocorticoids may be dispensable for its treatment.
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  • 文章类型: Journal Article
    多发性硬化症(MS)是一种使人衰弱的脱髓鞘疾病,其特征是由于少突胶质细胞前体细胞(OPCs)分化不足和异常星形胶质细胞增生而导致的髓鞘再生失败。临床标本的全面细胞图谱重新分析揭示了特定星形胶质细胞亚型中聚集蛋白(CLU)的表达与MS患者的活动性病变有关。我们的调查显示,患者组织的活跃病变和雌性鼠MS模型中星形胶质细胞CLU水平均升高。CLU给药刺激原发性星形胶质细胞增殖,同时阻碍星形胶质细胞介导的髓磷脂碎片清除。有趣的是,CLU过载直接阻碍OPC分化并诱导OPC和OLs凋亡。机械上,CLU通过极低密度脂蛋白受体抑制原发性OPCs中的PI3K-AKT信号传导.AKT的药理激活挽救了过量CLU对OPCs造成的损害,并改善了call体的脱髓鞘。此外,CLU的有条件敲除成为一种有希望的干预措施,在小鼠MS模型中展示了改善的髓鞘再生过程和降低的严重程度。
    Multiple sclerosis (MS) is a debilitating demyelinating disease characterized by remyelination failure attributed to inadequate oligodendrocyte precursor cells (OPCs) differentiation and aberrant astrogliosis. A comprehensive cell atlas reanalysis of clinical specimens brings to light heightened clusterin (CLU) expression in a specific astrocyte subtype links to active lesions in MS patients. Our investigation reveals elevated astrocytic CLU levels in both active lesions of patient tissues and female murine MS models. CLU administration stimulates primary astrocyte proliferation while concurrently impeding astrocyte-mediated clearance of myelin debris. Intriguingly, CLU overload directly impedes OPC differentiation and induces OPCs and OLs apoptosis. Mechanistically, CLU suppresses PI3K-AKT signaling in primary OPCs via very low-density lipoprotein receptor. Pharmacological activation of AKT rescues the damage inflicted by excess CLU on OPCs and ameliorates demyelination in the corpus callosum. Furthermore, conditional knockout of CLU emerges as a promising intervention, showcasing improved remyelination processes and reduced severity in murine MS models.
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  • 文章类型: Journal Article
    背景:镜像运动(MM)通常是由多发性硬化症(MS)也受影响的半球间通路缺陷引起的,尤其是call体。我们通过经颅磁刺激(TMS)研究了MM在MS中的患病率与功能和形态call骨纤维完整性的关系,磁共振成像(MRI),以及疲劳。
    方法:在21例复发缓解型MS患者和19例健康对照中,使用床边测试对MM进行评估和分级(Woods和Teuber量表:MM1-4)。使用运动和认知功能疲劳量表(FSMC)问卷评估疲劳。TMS测量同侧沉默期潜伏期和持续时间。MRI通过测量归一化的call体面积(nCCA)评估call骨萎缩,call体指数(CCI),和病变体积。
    结果:在MRI研究中,与健康对照组相比,MS患者的MM明显更频繁且明显(p=0.0002),nCCA明显更低(p=0.045)。MM评分较高的患者(MM>1vs.MM0/1)显示出明显更多的疲劳(更高的FSMC总和评分,p=0.04,运动评分,p=0.01)。在TMS和MRI研究中,在MM0/1和MM>1的患者之间没有发现显着差异(同侧沉默期测量,CCA,CCI和病变体积)。
    结论:MM在MS中很常见,可以通过床边测试轻松检测。由于MM与疲劳有关,它们可能表明MS的疲劳。可能是其他大脑结构,除了call体,可能有助于MM在MS中的起源。
    BACKGROUND: Mirror movements (MM) are commonly caused by a defect of interhemispheric pathways also affected in multiple sclerosis (MS), particularly the corpus callosum. We investigated the prevalence of MM in MS in relation to functional and morphological callosal fiber integrity by transcranial magnetic stimulation (TMS), magnetic resonance imaging (MRI), as well as fatigue.
    METHODS: In 21 patients with relapsing-remitting MS and 19 healthy controls, MM were assessed and graded (Woods and Teuber scale: MM 1-4) using a bedside test. Fatigue was evaluated using the Fatigue Scale for Motor and Cognitive Functions (FSMC) questionnaire. TMS measured ipsilateral silent period latency and duration. MRI assessed callosal atrophy by measuring the normalized corpus callosum area (nCCA), corpus callosum index (CCI), and lesion volume.
    RESULTS: MS patients had significantly more often and pronounced MM compared to healthy controls (p = 0.0002) and nCCA was significantly lower (p = 0.045) in MRI studies. Patients with higher MM scores (MM > 1 vs. MM 0/1) showed significantly more fatigue (higher FSMC sum score, p = 0.04, motor score, p = 0.01). In TMS and MRI studies, no significant differences were found between patients with MM 0/1 and those with MM > 1 (ipsilateral silent period measurements, CCA, CCI and lesion volume).
    CONCLUSIONS: MM are common in MS and can easily be detected through bedside testing. As MM are associated with fatigue, they might indicate fatigue in MS. It is possible that other cerebral structures, in addition to the corpus callosum, may contribute to the origin of MM in MS.
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  • 文章类型: Journal Article
    众所周知,灵长类杏仁核在同侧皮质的许多区域形成突起,但是它与对侧视觉皮层形成联系的程度仍然知之甚少。基于对the猴的逆行示踪剂注射,我们报告说,杏仁核形成广泛的投影到同侧的皮质外,包括V1和两个背侧的区域(MT,V4T,V3a,19M,和PG/PFG)和腹侧(VLP和TEO)流。此外,对侧投影被发现瞄准每个跨种族区域,但不是V1。在两个半球,示踪剂标记的神经元仅位于基底外侧核复合体中。相对于同侧连接,对侧杏仁核中标记的神经元数量较少(1.2%至5.8%)。对侧连接的百分比随着等级水平的增加而逐渐增加。在call体的注射表明,至少一些杏仁核-皮质连接穿过该纤维束,除了先前记录的通过前连合的路径。我们的结果将杏仁核投射的知识扩展到了跨皮质皮质,同时还揭示了传达情感内容的视觉刺激可以直接影响对侧视野中神经处理的早期阶段的途径。
    It is known that the primate amygdala forms projections to many areas of the ipsilateral cortex, but the extent to which it forms connections with the contralateral visual cortex remains less understood. Based on retrograde tracer injections in marmoset monkeys, we report that the amygdala forms widespread projections to the ipsilateral extrastriate cortex, including V1 and areas in both the dorsal (MT, V4T, V3a, 19M, and PG/PFG) and the ventral (VLP and TEO) streams. In addition, contralateral projections were found to target each of the extrastriate areas, but not V1. In both hemispheres, the tracer-labeled neurons were exclusively located in the basolateral nuclear complex. The number of labeled neurons in the contralateral amygdala was small relative to the ipsilateral connection (1.2% to 5.8%). The percentage of contralateral connections increased progressively with hierarchical level. An injection in the corpus callosum demonstrated that at least some of the amygdalo-cortical connections cross through this fiber tract, in addition to the previously documented path through the anterior commissure. Our results expand knowledge of the amygdalofugal projections to the extrastriate cortex, while also revealing pathways through which visual stimuli conveying affective content can directly influence early stages of neural processing in the contralateral visual field.
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  • 文章类型: Case Reports
    进行性多灶性白质脑病(PML)是一种罕见的中枢神经系统(CNS)脱髓鞘疾病,原因是约翰·坎宁安(JC)病毒在免疫功能低下的患者中最常见。脑干和前call体是白质病变的罕见位置。我们介绍了一名40岁女性的PML病例,该女性因急症室的强直性癫痫发作和短暂的后意识错乱而出现。住院患者检查显示分化细胞计数(CD3和CD4)低,转胺炎,阳性药物筛选,和异常脑电图(EEG)。头部的计算机断层扫描(CT)和大脑的磁共振图像(MRI或MR)显示,右半球的皮质下和脑室周围白质病变延伸到脑干和左额叶。医院课程包括支持性措施,癫痫发作治疗和预防,和人类免疫缺陷病毒(HIV)的管理以及预防性抗生素。患者在接受适当药物治疗和门诊转诊后出院。总的来说,这个案例描述了一些关键点。它突出了PML在HIV治疗不足的情况下的特殊成像特征。例如,白质病变穿过前call体而不是脾,如“杠铃”标志。此外,病变沿同侧皮质脊髓束向下延伸至中脑和脑桥。这可能是捕获这两个特征的首批案例之一,因为它们同时发生的情况很少。
    Progressive multifocal leukoencephalopathy (PML) is a rare demyelinating disease of the central nervous system (CNS) due to John Cunningham (JC) virus reactivation most often in immunocompromised patients. The brainstem and the anterior corpus callosum are uncommon locations for white matter lesions. We present a case of PML in a 40-year-old female presenting to the emergency department for a tonic seizure with transient postictal confusion. The inpatient workup revealed low cluster of differentiation cell counts (CD3 and CD4), transaminitis, positive drug screen, and abnormal electroencephalogram (EEG). The computed tomogram (CT) of the head and magnetic resonance image (MRI or MR) of the brain showed evidence of subcortical and periventricular white matter lesions in the right hemisphere extending into the brainstem and the left frontal lobe. The hospital course consisted of supportive measures, seizure treatment along with prophylaxis, and human immunodeficiency virus (HIV) management along with prophylactic antibiotics. The patient was discharged with appropriate medications and outpatient referrals. Overall, this case describes some key points. It highlights particular imaging characteristics of PML in the setting of inadequately treated HIV. For example, white matter lesions cross the anterior corpus callosum rather than the splenium, as in the \"barbell\" sign. In addition, the lesions extend inferiorly along the ipsilateral corticospinal tract into the midbrain and pons. This could be one of the first cases to capture both of these features given the rarity of their concomitant occurrence.
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  • 文章类型: Journal Article
    大脑不对称是人类大脑的一个决定性特征,但是关于大脑结构不对称和call体尺寸之间的关系存在一些争议,大脑的主要半球间连合。一方面,更不对称的大脑可能容纳比例较小的call体(负链接),可能是由于半球内连接在半球间连接上占主导地位。另一方面,不对称的大脑可能含有成比例较大的call体(正链接),为了促进可能增加的半球间交流需求,通过兴奋性或抑制性通道。关于这个主题的科学文献相对稀疏,但是我们已经确定了13项直接评估结构不对称性与call体形态之间关系的研究。这些研究表明,对全球有多种影响,区域,和地方层面,发现范围从负面联系,积极的联系,没有任何联系。对这些联系进行了系统的总结,detailed,并在本综述中讨论。研究结果之间的差异可能来自不同形态计量学方法的应用,对可能混淆的区别对待,以及研究样本的大小和特征。
    Cerebral asymmetry is a defining feature of the human brain, but some controversy exists with respect to the relationship between structural brain asymmetry and the dimensions of the corpus callosum, the brain\'s major inter-hemispheric commissure. On the one hand, more asymmetric brains might house a proportionally smaller corpus callosum (negative link), potentially due to intra-hemispheric connections dominating over inter-hemispheric connections. On the other hand, asymmetric brains may contain a proportionately larger corpus callosum (positive link), to facilitate a possibly enhanced demand of interhemispheric communication, either through excitatory or inhibitory channels. The scientific literature on this topic is relatively sparse, but we have identified 13 studies that directly assess the relationship between structural asymmetries and callosal morphology. The studies suggest a multitude of effects on the global, regional, and local levels, where findings range from negative links, to positive links, to no links whatsoever. These links are systematically summarized, detailed, and discussed in the present review. Discrepancies between study outcomes might arise from the application of different morphometric approaches, the differential treatment of possible confounds, as well as the size and characteristics of the study sample.
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  • 文章类型: Journal Article
    远端大脑前动脉(DACA)的动脉瘤很少见,但手术具有挑战性。尽管已知DACA领土上的动脉瘤位置具有治疗意义,关于其临床和预后意义的文献尚不清楚.我们在过去5年的手术经验进行了回顾,以比较临床,Operative,以及位于call体genu中部以下的动脉瘤(称为近端动脉瘤)与该点远端的动脉瘤(称为远端动脉瘤)之间的结果特征。使用单变量和多变量分析进行预后因素分析。总共治疗了34例患者(M:F=1:2.3)。与(n=2,13.3%)近端动脉瘤(p=0.039)相比,远端组的不良临床分级频率更高(n=9,47.4%)。尽管这些患者总体上有延迟功能改善的趋势,结果主要归因于近端组的有利结局(出院时和最后一次随访时的有利功能结局分别为80%和86.7%).在多变量分析中,在演示(OR=13.75;95CI=1.2-157.7)(p=0.035)和应用临时剪辑(AOR=34.32;95CI=2.59-454.1)(p=0.007)时,只有WFNS等级(>2),两者在远端组中都更多,独立预测长期功能结局不佳。因此,动脉瘤位置影响术前临床分级,术中动脉瘤破裂风险率以及临时夹闭要求。这些因素的组合导致远端DACA动脉瘤的短期和长期功能结果更差。
    Aneurysms of the distal anterior cerebral artery (DACA) are rare but surgically challenging. Despite a known therapeutic implication of the aneurysm location on the DACA territory, the literature is unclear about its clinical and prognostic significance. Our surgical experience over the last 5 years was reviewed to compare the clinical, operative, and outcome characteristics between aneurysms located below the mid portion of the genu of the corpus callosum (called proximal aneurysms) to those distal to this point (called distal aneurysms). A prognostic factor analysis was done using uni and multivariable analysis. A total of 34 patients were treated (M: F = 1:2.3). The distal group had a higher frequency of poor clinical grade at presentation (n = 9, 47.4%) in contrast to (n = 2, 13.3%) proximal aneurysms (p = 0.039). Despite an overall tendency for a delayed functional improvement in these patients, the results were mainly due to favorable outcomes in the proximal group (favourable functional outcomes at discharge and at last follow-up being 80% and 86.7% respectively). On the multivariable analysis, only WFNS grade (> 2) at presentation (OR = 13.75; 95CI = 1.2-157.7) (p = 0.035) and application of temporary clips (AOR = 34.32; 95CI = 2.59-454.1) (p = 0.007), both of which were more in the distal group, independently predicted a poor long term functional outcome. Thus, the aneurysm location impacts the preoperative clinical grade, the intraoperative aneurysm rupture risk rate as well as the temporary clipping requirement. A combination of these factors leads to worse short and long-term functional outcomes in the distal DACA aneurysms.
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  • 文章类型: Journal Article
    脑小血管病(cSVD)是血管性混合性认知障碍(CI)的主要病因之一,它是相关联的,特别是,大脑老化了解cSVD中完整脑白质的结构组织变化可能会使人们开发出敏感的生物标志物,以进行早期诊断和监测疾病进展。
    目的:使用扩散MRI(D-MRI)方法评估不同程度CI的cSVD患者call体(CC)的微观结构变化,并揭示扩散指标与CI的最敏感相关性。
    方法:该研究包括166名cSVD患者(51.8%女性;60.4±7.6岁)和44名健康志愿者(65.9%女性;59.6±6.8岁)。所有受试者均接受D-MRI(3T)信号(弥散张量和峰度)和生物物理(神经突方向弥散和密度成像,NODDI,白质道完整性,WMTI,多室球形平均技术,MC-SMT)在三个CC部分进行建模以及神经心理学评估。
    结果:在cSVD患者中,在已经处于主观CI阶段的所有CC段中发现了微观结构变化,被发现恶化为mildCI和痴呆症。在小镊子中观察到更明显的变化。在信号模型FA中,MD,MK,RD,还有RK,以及在生物物理模型中,MC-SMT(EMD,ETR)和WMTI(AWF)指标表现出最大的曲线下面积(>0.85),表征微结构完整性的损失,潜在脱髓鞘的严重程度,以及轴突内水的比例,分别。结论:该研究揭示了先进的D-MRI方法对评估cSVD脑组织变化的相关性。鉴定的扩散生物标志物可用于CI进展的澄清和观察。
    The cerebral small vessel disease (cSVD) is one of the main causes of vascular and mixed cognitive impairment (CI), and it is associated, in particular, with brain ageing. An understanding of structural tissue changes in an intact cerebral white matter in cSVD might allow one to develop the sensitive biomarkers for early diagnosis and monitoring of disease progression.
    OBJECTIVE: to evaluate microstructural changes in the corpus callosum (CC) using diffusion MRI (D-MRI) approaches in cSVD patients with different severity of CI and reveal the most sensitive correlations of diffusion metrics with CI.
    METHODS: the study included 166 cSVD patients (51.8% women; 60.4 ± 7.6 years) and 44 healthy volunteers (65.9% women; 59.6 ± 6.8 years). All subjects underwent D-MRI (3T) with signal (diffusion tensor and kurtosis) and biophysical (neurite orientation dispersion and density imaging, NODDI, white matter tract integrity, WMTI, multicompartment spherical mean technique, MC-SMT) modeling in three CC segments as well as a neuropsychological assessment.
    RESULTS: in cSVD patients, microstructural changes were found in all CC segments already at the subjective CI stage, which was found to worsen into mild CI and dementia. More pronounced changes were observed in the forceps minor. Among the signal models FA, MD, MK, RD, and RK, as well as among the biophysical models, MC-SMT (EMD, ETR) and WMTI (AWF) metrics exhibited the largest area under the curve (>0.85), characterizing the loss of microstructural integrity, the severity of potential demyelination, and the proportion of intra-axonal water, respectively. Conclusion: the study reveals the relevance of advanced D-MRI approaches for the assessment of brain tissue changes in cSVD. The identified diffusion biomarkers could be used for the clarification and observation of CI progression.
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  • 文章类型: Journal Article
    脊椎动物神经系统中形成髓磷脂的少突胶质细胞共表达转录因子Sox10及其同源物Sox8。虽然Sox10在少突胶质细胞发育的所有阶段都起着至关重要的作用,包括终末分化,Sox8的丢失仅导致轻度和瞬态扰动。这里,我们旨在阐明这些转录因子在成人完全分化少突胶质细胞和髓鞘维持中的作用和相互关系.为此,我们在两个月大的小鼠的大脑中进行了Sox10,Sox8或两者的靶向缺失。删除后三周,所得到的小鼠突变体均未表现出少突胶质细胞数量的显著改变,髓鞘计数,髓鞘超微结构,或者call体的髓磷脂蛋白水平,尽管有效的基因失活。然而,在Sox10或Sox8/Sox10联合缺失的小鼠中观察到髓磷脂基因表达的差异。对解剖的call体进行的RNA测序分析证实,在合并缺失的小鼠中,少突胶质细胞表达谱发生了实质性变化,而在仅Sox10缺失的小鼠中,少突胶质细胞表达谱发生了更微妙的变化。值得注意的是,Sox8缺失不影响与少突胶质细胞的分化状态或髓磷脂完整性相关的表达谱的任何方面。这些发现扩展了我们对Sox8和Sox10在成年少突胶质细胞中的作用的理解,并对旁系同源物之间的功能关系和潜在的分子机制具有重要意义。
    Myelin-forming oligodendrocytes in the vertebrate nervous system co-express the transcription factor Sox10 and its paralog Sox8. While Sox10 plays crucial roles throughout all stages of oligodendrocyte development, including terminal differentiation, the loss of Sox8 results in only mild and transient perturbations. Here, we aimed to elucidate the roles and interrelationships of these transcription factors in fully differentiated oligodendrocytes and myelin maintenance in adults. For that purpose, we conducted targeted deletions of Sox10, Sox8, or both in the brains of two-month-old mice. Three weeks post-deletion, none of the resulting mouse mutants exhibited significant alterations in oligodendrocyte numbers, myelin sheath counts, myelin ultrastructure, or myelin protein levels in the corpus callosum, despite efficient gene inactivation. However, differences were observed in the myelin gene expression in mice with Sox10 or combined Sox8/Sox10 deletion. RNA-sequencing analysis on dissected corpus callosum confirmed substantial alterations in the oligodendrocyte expression profile in mice with combined deletion and more subtle changes in mice with Sox10 deletion alone. Notably, Sox8 deletion did not affect any aspects of the expression profile related to the differentiated state of oligodendrocytes or myelin integrity. These findings extend our understanding of the roles of Sox8 and Sox10 in oligodendrocytes into adulthood and have important implications for the functional relationship between the paralogs and the underlying molecular mechanisms.
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  • 文章类型: Journal Article
    先前的几项研究报告说,与有视力的人群相比,盲人参与者的样本向左偏侧化减少。这种差异的起源仍然未知。这里,我们测试了功能偏侧化是否与白质束的结构特征有关[call体(CC),钩肌束(UF),和上纵束(SLF)],正如以前在典型视力人群中进行的研究所表明的那样。在功能磁共振成像期间对23名盲人和21名有视力的成人参与者进行了测试,语义决策范式在听觉上和适合阅读的方式(实际上是盲人,视觉上是盲人)。侧化指数(LI)基于激活量计算。从感兴趣的白质束提取分数各向异性(FA)量度。进行了相关分析,测试了FA和LI之间的关系。复制了语音处理和与阅读相关的激活的减少的向左偏侧化。然而,CC和LI的结构完整性以及半球内束和LI的不对称性之间的关系未得到证实,可能是由于缺乏力量。在缺乏感觉的人群中,语言网络偏侧化减少的来源仍然未知。进一步的研究应考虑环境变量(例如,与书面语言接触的频率)以及可能影响人脑功能偏侧化的因素的复杂性。
    Several previous studies reported reduced leftward lateralization in blind participants\' samples compared to the sighted population. The origins of this difference remain unknown. Here, we tested whether functional lateralization is connected with the structural characteristics of white matter tracts [corpus callosum (CC), uncinate fasciculus (UF), and superior longitudinal fasciculus (SLF)], as suggested by previous studies conducted in the typical sighted population. Twenty-three blind and 21 sighted adult participants were tested during fMRI with a semantic decision paradigm presented both auditorily and in the modality appropriate for reading (tactually for the blind and visually for the sighted). Lateralization indices (LI) were calculated based on the activations. The fractional anisotropy (FA) measure was extracted from the white matter tracts of interest. Correlation analyses testing the relationship between FA and LI were conducted. The reduced leftward lateralization of both speech processing and reading-related activations was replicated. Nevertheless, the relationship between the structural integrity of the CC and LI and between the asymmetry of the intrahemispheric tracts and LI was not confirmed, possibly due to the lack of power. The sources of the reduced lateralization of the language network in the sensory-deprived population remain unknown. Further studies should account for environmental variables (e.g., the frequency of contact with written language) and the complexity of the factors that may influence the functional lateralization of the human brain.
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