• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
The relationship between uric acid levels and Huntington's disease progression.尿酸水平与亨廷顿病进展之间的关系。
Mov Disord. 2010 Jan 30;25(2):224-8. doi: 10.1002/mds.22907.
2
Rate of functional decline in Huntington's disease. Huntington Study Group.亨廷顿病的功能衰退率。亨廷顿研究小组。
Neurology. 2000 Jan 25;54(2):452-8. doi: 10.1212/wnl.54.2.452.
3
Huntington's Disease Progression: A Population Modeling Approach to Characterization Using Clinical Rating Scales.亨廷顿病进展:使用临床评分量表进行特征描述的人群建模方法。
J Clin Pharmacol. 2020 Aug;60(8):1051-1060. doi: 10.1002/jcph.1598. Epub 2020 May 16.
4
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.鉴定与亨廷顿病进展相关的遗传变异:全基因组关联研究。
Lancet Neurol. 2017 Sep;16(9):701-711. doi: 10.1016/S1474-4422(17)30161-8. Epub 2017 Jun 20.
5
Clinical characterization of dystonia in adult patients with Huntington's disease.亨廷顿病成年患者的肌张力障碍临床特征。
Eur J Neurol. 2017 Sep;24(9):1140-1147. doi: 10.1111/ene.13349. Epub 2017 Jun 29.
6
The relationship between CAG repeat length and clinical progression in Huntington's disease.亨廷顿舞蹈病中CAG重复序列长度与临床进展的关系。
Mov Disord. 2008 Jul 15;23(9):1223-7. doi: 10.1002/mds.21988.
7
Complex movement behaviour and progression of Huntington's disease.亨廷顿舞蹈症的复杂运动行为与病情进展
Neurosci Lett. 2007 Apr 18;416(3):272-4. doi: 10.1016/j.neulet.2007.02.027. Epub 2007 Feb 11.
8
Total functioning capacity scale in Huntington's disease: natural course over time.亨廷顿舞蹈症的总功能能力量表:随时间的自然病程
J Neurol. 2025 Jan 15;272(2):140. doi: 10.1007/s00415-024-12771-w.
9
Serum neurofilament light chain but not serum glial fibrillary acidic protein is a marker of early Huntington's disease.血清神经丝轻链而非血清胶质纤维酸性蛋白是早期亨廷顿病的一个标志物。
J Neurol. 2025 Feb 1;272(2):174. doi: 10.1007/s00415-025-12901-y.
10
The use of quantitative oculometry in the assessment of Huntington's disease.定量眼测量法在亨廷顿舞蹈症评估中的应用。
Exp Brain Res. 2006 Feb;169(2):237-45. doi: 10.1007/s00221-005-0143-6. Epub 2005 Nov 5.

引用本文的文献

1
Metabolomics: a new frontier in neurodegenerative disease biomarker discovery.代谢组学:神经退行性疾病生物标志物发现的新前沿。
Metabolomics. 2025 May 15;21(3):67. doi: 10.1007/s11306-025-02267-7.
2
Xanthine Oxidoreductase: A Double-Edged Sword in Neurological Diseases.黄嘌呤氧化还原酶:神经疾病中的一把双刃剑
Antioxidants (Basel). 2025 Apr 17;14(4):483. doi: 10.3390/antiox14040483.
3
Advances in Huntington's Disease Biomarkers: A 10-Year Bibliometric Analysis and a Comprehensive Review.亨廷顿舞蹈症生物标志物的进展:十年文献计量分析与综合综述
Biology (Basel). 2025 Jan 26;14(2):129. doi: 10.3390/biology14020129.
4
Uric Acid Mitigates Cognitive Deficits via TFEB-Mediated Microglial Autophagy in Mice Models of Alzheimer's Disease.尿酸通过 TFEB 介导的小胶质细胞自噬减轻阿尔茨海默病小鼠模型的认知缺陷。
Mol Neurobiol. 2024 Jun;61(6):3678-3696. doi: 10.1007/s12035-023-03818-6. Epub 2023 Nov 27.
5
The effect of danger-associated molecular patterns on survival in acute graft versus host disease.危险相关分子模式对急性移植物抗宿主病生存的影响。
Bone Marrow Transplant. 2024 Feb;59(2):189-195. doi: 10.1038/s41409-023-02145-7. Epub 2023 Nov 7.
6
Uric acid and glaucoma: a systematic review and meta-analysis.尿酸与青光眼:一项系统评价和荟萃分析
Front Med (Lausanne). 2023 Jul 28;10:1159316. doi: 10.3389/fmed.2023.1159316. eCollection 2023.
7
Investigating the Dietary Intake Using the CyFFQ Semi-Quantitative Food Frequency Questionnaire in Cypriot Huntington's Disease Patients.使用 CyFFQ 半定量食物频率问卷调查塞浦路斯亨廷顿病患者的饮食摄入情况。
Nutrients. 2023 Feb 23;15(5):1136. doi: 10.3390/nu15051136.
8
The updated development of blood-based biomarkers for Huntington's disease.用于亨廷顿病的基于血液的生物标志物的最新进展。
J Neurol. 2023 May;270(5):2483-2503. doi: 10.1007/s00415-023-11572-x. Epub 2023 Jan 24.
9
Uric Acid Enhances Neurogenesis in a Parkinsonian Model by Remodeling Mitochondria.尿酸通过重塑线粒体在帕金森病模型中增强神经发生。
Front Aging Neurosci. 2022 Jun 2;14:851711. doi: 10.3389/fnagi.2022.851711. eCollection 2022.
10
The Influence of Serum Uric Acid on the Brain and Cognitive Dysfunction.血清尿酸对大脑及认知功能障碍的影响
Front Psychiatry. 2022 Apr 22;13:828476. doi: 10.3389/fpsyt.2022.828476. eCollection 2022.

本文引用的文献

1
The relationship between CAG repeat length and clinical progression in Huntington's disease.亨廷顿舞蹈病中CAG重复序列长度与临床进展的关系。
Mov Disord. 2008 Jul 15;23(9):1223-7. doi: 10.1002/mds.21988.
2
Serum urate as a predictor of clinical and radiographic progression in Parkinson disease.血清尿酸作为帕金森病临床和影像学进展的预测指标。
Arch Neurol. 2008 Jun;65(6):716-23. doi: 10.1001/archneur.2008.65.6.nct70003. Epub 2008 Apr 14.
3
Oxidative damage in Huntington's disease pathogenesis.亨廷顿舞蹈病发病机制中的氧化损伤
Antioxid Redox Signal. 2006 Nov-Dec;8(11-12):2061-73. doi: 10.1089/ars.2006.8.2061.
4
Decreased plasma antioxidants in patients with Alzheimer's disease.阿尔茨海默病患者血浆抗氧化剂水平降低。
Int J Geriatr Psychiatry. 2006 Apr;21(4):344-8. doi: 10.1002/gps.1469.
5
Serum uric acid levels and the risk of Parkinson disease.血清尿酸水平与帕金森病风险
Ann Neurol. 2005 Nov;58(5):797-800. doi: 10.1002/ana.20663.
6
Mitochondria take center stage in aging and neurodegeneration.线粒体在衰老和神经退行性变过程中占据核心地位。
Ann Neurol. 2005 Oct;58(4):495-505. doi: 10.1002/ana.20624.
7
A randomized, placebo-controlled trial of coenzyme Q10 and remacemide in Huntington's disease.辅酶Q10与瑞玛西胺治疗亨廷顿舞蹈症的随机安慰剂对照试验。
Neurology. 2001 Aug 14;57(3):397-404. doi: 10.1212/wnl.57.3.397.
8
Construct and concurrent validity of the Hopkins Verbal Learning Test-revised.霍普金斯词语学习测验修订版的结构效度和同时效度。
Clin Neuropsychol. 1999 Aug;13(3):348-58. doi: 10.1076/clin.13.3.348.1749.
9
Uric acid protects neurons against excitotoxic and metabolic insults in cell culture, and against focal ischemic brain injury in vivo.尿酸在细胞培养中可保护神经元免受兴奋性毒性和代谢损伤,在体内可保护神经元免受局灶性缺血性脑损伤。
J Neurosci Res. 1998 Sep 1;53(5):613-25. doi: 10.1002/(SICI)1097-4547(19980901)53:5<613::AID-JNR11>3.0.CO;2-1.
10
Unified Huntington's Disease Rating Scale: reliability and consistency. Huntington Study Group.统一亨廷顿病评定量表:可靠性与一致性。亨廷顿研究小组。
Mov Disord. 1996 Mar;11(2):136-42. doi: 10.1002/mds.870110204.

尿酸水平与亨廷顿病进展之间的关系。

The relationship between uric acid levels and Huntington's disease progression.

机构信息

Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14620, USA.

出版信息

Mov Disord. 2010 Jan 30;25(2):224-8. doi: 10.1002/mds.22907.

DOI:10.1002/mds.22907
PMID:20063429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2831113/
Abstract

Uric acid (UA) may be associated with the progression of Parkinson's disease and related neurodegenerative conditions; however, its association with Huntington's disease (HD) progression has not been explored. A secondary analysis of 347 subjects from the CARE-HD clinical trial was performed to examine the relationship between baseline UA levels and the level of functional decline in HD. Outcomes included change in scores at 30 months for the Unified Huntington's Disease Rating Scale components. There was less worsening of total functional capacity over time with increasing baseline UA levels (adjusted mean worsening in scores: 3.17, 2.99, 2.95, 2.28, 2.21, from lowest to highest UA quintile, P = 0.03). These data suggest a possible association between higher UA levels and slower HD progression, particularly as measured by total functional capacity. If confirmed, UA could be an important predictor and potentially modifiable factor affecting the rate of HD progression.

摘要

尿酸(UA)可能与帕金森病和相关神经退行性疾病的进展有关;然而,其与亨廷顿病(HD)进展的关系尚未得到探索。对 CARE-HD 临床试验的 347 名受试者进行了二次分析,以检查基线 UA 水平与 HD 功能下降水平之间的关系。结果包括在 30 个月时统一亨廷顿病评定量表各组成部分的评分变化。随着基线 UA 水平的升高,总功能能力的恶化程度随着时间的推移而降低(调整后的评分恶化:3.17、2.99、2.95、2.28、2.21,从最低到最高 UA 五分位数,P = 0.03)。这些数据表明,UA 水平较高与 HD 进展较慢之间可能存在关联,特别是用总功能能力来衡量。如果得到证实,UA 可能是影响 HD 进展速度的一个重要预测指标和潜在可改变的因素。