Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, 1060 William Moore Dr., Raleigh, NC, 27607, USA.
Department of Medicine, Duke University Medical Center, Durham, NC, 27710, USA.
Mol Neurobiol. 2020 Jul;57(7):3143-3149. doi: 10.1007/s12035-020-01951-0. Epub 2020 May 30.
Age is a primary risk factor for multiple comorbidities including neurodegenerative diseases. Pet dogs and humans represent two populations that have experienced a significant increase in average life expectancy over the last century. A higher prevalence of age-related neurodegenerative diseases has been observed across both species, and human diseases, such as Alzheimer's disease (AD) and amyotrophic lateral sclerosis (ALS), have canine analogs, canine cognitive dysfunction (CCD), and degenerative myelopathy (DM) respectively. In humans, protein biomarkers have proved useful in the prediction and diagnosis of neurodegeneration. Molecular signatures of many proteins are highly conserved across species. In this study, we explored the potential of the neuronal cytoskeletal protein neurofilament light chain (NfL) as a biomarker of neuro-aging in dogs using an ultrasensitive single-molecule array assay to measure plasma concentrations. Healthy dogs of different ages and dogs affected with CCD and DM were evaluated. The mean plasma NfL concentrations in the different age groups of the healthy population were as follows: 4.55 ± 1.70 pg/mL in puppy/junior group (0.43-2 years), 13.51 ± 6.8 pg/mL in adult/mature group (2.1-9 years), and 47.1 ± 12.68 pg/mL in geriatric/senior group (9.3-14.5 years). Concentrations in dogs with DM (7.5-12.6 years) and CCD (11.0-15.6 years) were 84.17 ± 53.57 pg/mL and 100.73 ± 83.72 pg/mL, respectively. Plasma NfL increases in an age-dependent manner and is significantly elevated in dogs diagnosed with neurodegenerative disease. This work identified plasma NfL as a key clinical index of neuro-aging and neurodegeneration in pet dogs. Our findings mirror recent reports from human neurodegenerative diseases.
年龄是多种合并症的主要危险因素,包括神经退行性疾病。宠物狗和人类是过去一个世纪中平均预期寿命显著延长的两个群体。这两个物种都观察到了与年龄相关的神经退行性疾病的患病率更高,人类疾病,如阿尔茨海默病(AD)和肌萎缩侧索硬化症(ALS),分别有犬类对应疾病,即犬认知功能障碍(CCD)和退行性脊髓病(DM)。在人类中,蛋白质生物标志物已被证明可用于预测和诊断神经退行性变。许多蛋白质的分子特征在物种间高度保守。在这项研究中,我们使用超灵敏的单分子阵列分析来测量血浆浓度,探索神经元细胞骨架蛋白神经丝轻链(NfL)作为犬神经老化生物标志物的潜力。评估了不同年龄的健康犬、患有 CCD 和 DM 的犬。健康人群不同年龄组的平均血浆 NfL 浓度如下:幼犬/青少年组(0.43-2 岁)为 4.55±1.70 pg/mL,成年/成熟组(2.1-9 岁)为 13.51±6.8 pg/mL,老年/老年组(9.3-14.5 岁)为 47.1±12.68 pg/mL。DM(7.5-12.6 岁)和 CCD(11.0-15.6 岁)犬的浓度分别为 84.17±53.57 pg/mL 和 100.73±83.72 pg/mL。血浆 NfL 随年龄呈依赖性增加,并在诊断为神经退行性疾病的犬中显著升高。这项工作确定了血浆 NfL 是宠物犬神经老化和神经退行性变的关键临床指标。我们的发现与最近人类神经退行性疾病的报告相吻合。