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Vitamin B12 measurements across neurodegenerative disorders

机译:维生素B12横跨神经变性障碍的测量

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Vitamin B12 deficiency causes a number of neurological features including cognitive and psychiatric disturbances, gait instability, neuropathy, and autonomic dysfunction. Clinical recognition of B12 deficiency in neurodegenerative disorders is more challenging because it causes defects that overlap with expected disease progression. We sought to determine whether B12 levels at the time of diagnosis in patients with Parkinson’s disease (PD) differed from those in patients with other neurodegenerative disorders. We performed a cross-sectional analysis of B12 levels obtained around the time of diagnosis in patients with PD, Multiple System Atrophy (MSA), Dementia with Lewy Bodies (DLB), Alzheimer’s disease (AD), Progressive Supranuclear Palsy (PSP), Frontotemporal Dementia (FTD), or Mild Cognitive Impairment (MCI). We also evaluated the rate of B12 decline in PD, AD, and MCI. In multivariable analysis adjusted for age, sex, and B12 supplementation, we found that B12 levels were significantly lower at time of diagnosis in patients with PD than in patients with PSP, FTD, and DLB. In PD, AD, and MCI, the rate of B12 decline ranged from ??17 to ??47?pg/ml/year, much greater than that reported for the elderly population. Further studies are needed to determine whether comorbid B12 deficiency affects progression of these disorders.
机译:维生素B12缺陷导致许多神经功能特征,包括认知和精神病障碍,步态不稳定,神经病和自主功能障碍。 N12缺乏神经变性障碍的临床识别更具挑战性,因为它导致与预期疾病进展重叠的缺陷。我们试图确定帕金森病(PD)诊断时的B12水平是否与其他神经变性障碍患者的患者不同。我们对PD患者诊断时的B12水平进行了横截面分析,多系统萎缩(MSA),痴呆症,具有石油体(DLB),Alzheimer疾病(AD),进步性激素麻痹(PSP),额颞扑痴呆症(FTD),或轻度认知障碍(MCI)。我们还评估了PD,AD和MCI中的B12下降率。在适应年龄,性别和B12补充的多变量分析中,我们发现,PD患者的诊断时间比PSP,FTD和DLB患者在诊断时明显较低。在PD,AD和MCI中,B12的速度范围为17到?? 47?pg / ml /年,远远大于老年人的报告。需要进一步的研究来确定合并B12缺乏是否会影响这些疾病的进展。

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