Kamis Danielle, Stratton Lee, Calvó María, Padilla Eduardo, Florenzano Néstor, Guerrero Gonzalo, Molina Rangeon Beatriz, Molina Juan, de Erausquin Gabriel A
Roskamp Laboratory of Brain Development, Modulation and Repair, University of South Florida, United States.
Hospital Neuropsiquiátrico Néstor Sequeiros, Ministerio de Salud, Provincia de Jujuy, Argentina; Fundación de Lucha contra los Trastornos Neurológicos y Psiquiátricos en Minorías (FULTRA), Argentina.
Schizophr Res. 2015 May;164(1-3):250-5. doi: 10.1016/j.schres.2015.01.035. Epub 2015 Feb 27.
We tested the hypothesis that loss of substantia nigra neurons in subjects at risk of schizophrenia (1), as reflected by midbrain hyperechogenicity (2) and parkinsonian motor impairment (3), is asymmetric and influenced by sex. We evaluated 62 subjects with never-treated chronic schizophrenia, 80 of their adult, unaffected first degree relatives and 62 healthy controls (matched by sex and age to the cases), part of an Andean population of Northern Argentina. Parkinsonism was scored blindly using UPDRS-3 (Unified Parkinson's Disease Rating Scale) on videotaped exams by 2 independent raters. Transcranial ultrasound was performed by an expert sonographist blind to subject condition with a 2.5 MHz transducer through a temporal bone window. Quantification of echogenic area was carried out on saved images by a different evaluator. We found a significant difference in parkinsonian motor impairment between patients, their relatives as well as controls. All three groups showed worse parkinsonism on the left side than the right, corresponding with increased echogenicity on the right substantia nigra compared with the left. Females had significantly more right echogenicity than males, and patients and unaffected relatives were significantly more echogenic than controls on that side. On the left, only female patients had significant echogenicity. Our data supports the notion that unaffected relatives of schizophrenic subjects have increased parkinsonism and concomitant brainstem abnormalities which may represent a vulnerability to the disease. Both motor and brainstem abnormalities are asymmetric and influenced by sex.
在有精神分裂症风险的受试者中,黑质神经元的丧失(1),如通过中脑高回声(2)和帕金森氏运动障碍(3)所反映的,是不对称的且受性别影响。我们评估了62例未经治疗的慢性精神分裂症患者、他们80名未患病的成年一级亲属以及62名健康对照者(按性别和年龄与病例匹配),这些人来自阿根廷北部安第斯人群。帕金森症通过统一帕金森病评定量表(UPDRS - 3)由2名独立评估者在录像检查中进行盲法评分。经颅超声由一名对受试者情况不知情的专业超声医师通过颞骨窗使用2.5兆赫探头进行。回声区域的量化由另一名评估者在保存的图像上进行。我们发现患者、他们的亲属以及对照者在帕金森氏运动障碍方面存在显著差异。所有三组在左侧的帕金森症都比右侧更严重,这与右侧黑质比左侧回声增强相对应。女性右侧的回声显著多于男性,并且在该侧患者和未患病亲属的回声显著多于对照者。在左侧,只有女性患者有显著的回声。我们的数据支持这样一种观点,即精神分裂症患者的未患病亲属帕金森症增加且伴有脑干异常,这可能代表了对该疾病的易感性。运动和脑干异常都是不对称的且受性别影响。