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N6-methyladenine-modified DNA was decreased in Alzheimer’s disease patients
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作者 Shuang Lv Xiao Zhou +5 位作者 Yi-Ming Li Tao Yang Shu-Juan Zhang Yu Wang Shu-Hong Jia dan-tao peng 《World Journal of Clinical Cases》 SCIE 2022年第2期448-457,共10页
BACKGROUND In recent years,the prevalence of Alzheimer’s disease(AD)has increased,which places a great burden on society and families and creates considerable challenges for medical services.N6-methyladenine(m6A)deox... BACKGROUND In recent years,the prevalence of Alzheimer’s disease(AD)has increased,which places a great burden on society and families and creates considerable challenges for medical services.N6-methyladenine(m6A)deoxyribonucleic acid(DNA)adenine methylation is a novel biomarker and is abundant in the brain,but less common in AD.We support to analyze the relationship between DNA m6A and cognition in patients with AD and normal controls(NCs)in China.AIM To analyze the relationship between the novel m6A DNA and cognition in patients with AD and NCs in China.METHODS A total of 179 AD patients(mean age 71.60±9.89 years;males:91;females:88)and 147 NCs(mean age 69.59±11.22 years;males:77;females:70)who were age-and sex-matched were included in our study.All subjects underwent neuropsychological scale assessment and magnetic resonance imaging examination.Apolipoprotein E(APOE)genotypes were measured through agarose gel electrophoresis.Global m6A levels were evaluated by a MethylFlash m6A DNA Methylation ELISA Kit(colorimetric).Global m6A levels in total DNA from ten AD patients with 18F-AV-45(florbetapir)positron emission tomography(PET)positivity and ten NCs with PET negativity were analyzed by dot blotting to determine the results.RESULTS Our ELISA results showed that the global m6A DNA levels in peripheral blood were different between patients with AD and NCs(P=0.002;<0.05).And ten AD patients who were PET positive and ten NCs who were PET negative also showed the same results through dot blotting.There were significant differences between the two groups,which indicated that the leukocyte m6A DNA levels were different(P=0.005;<0.05).The m6A level was approximately 8.33%lower in AD patients than in NCs(mean 0.011±0.006 vs 0.012±0.005).A significant correlation was found between the Montreal Cognitive Assessment score and the peripheral blood m6A level in the tested population(r=0.143,P=0.01;<0.05).However,no relationship was found with APOEε4(P=0.633,>0.05).Further studies should be performed to validate these findings.CONCLUSION Our results show that reduced global m6A DNA methylation levels are significantly lower in AD patients than in NCs by approximately 8.33%in China. 展开更多
关键词 Alzheimer disease N6-methyladenine DNA Montreal Cognitive Assessment Apolipoprotein E Cognitive dysfunction
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Clinical and genetic study of ataxia with vitamin E deficiency: A case report
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作者 Lin-Wei Zhang Bing Liu dan-tao peng 《World Journal of Clinical Cases》 SCIE 2022年第23期8271-8276,共6页
BACKGROUND Ataxia with vitamin E deficiency(AVED)is a type of autosomal recessive cerebellar ataxia.Clinical manifestations include progressive cerebellar ataxia and movement disorders.TTPA gene mutations cause the di... BACKGROUND Ataxia with vitamin E deficiency(AVED)is a type of autosomal recessive cerebellar ataxia.Clinical manifestations include progressive cerebellar ataxia and movement disorders.TTPA gene mutations cause the disease.CASE SUMMARY We report the case of a 32-year-old woman who presented with progressive cerebellar ataxia,dysarthria,dystonic tremors and a remarkably decreased serum vitamin E concentration.Brain magnetic resonance images showed that her brainstem and cerebellum were within normal limits.Acquired causes of ataxia were excluded.Whole exome sequencing subsequently identified a novel homozygous variant(c.473T>C,p.F158S)of the TPPA gene.Bioinformatic analysis predicted that F185S is harmful to protein function.After supplementing the patient with vitamin E 400 mg three times per day for 2 years,her symptoms remained stable.CONCLUSION We identified an AVED patient caused by novel mutation in TTPA gene.Our findings widen the known TTPA gene mutation spectrum. 展开更多
关键词 Ataxia with vitamin E deficiency TTPA gene TREMOR Case report
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Amide Proton Transfer Magnetic Resonance Imaging of Alzheimer's Disease at 3.0 Tesla: A Preliminary Study 被引量:23
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作者 Rui Wang Sa-Ying Li +4 位作者 Min Chen Jin-Yuan Zhou dan-tao peng Chen Zhang Yong-Ming Dai 《Chinese Medical Journal》 SCIE CAS CSCD 2015年第5期615-619,共5页
关键词 磁共振成像 阿尔茨海默氏病 特斯拉 酰胺 MMSE 状态检查 分子诊断 APT
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Chinese expert consensus on the diagnosis of cardiogenic stroke(2019) 被引量:3
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作者 Guang-Zhi Liu Rong Hu +2 位作者 dan-tao peng Geriatric Neurology Grop,Geriatric Branch of Chinese Medical Association Writing Group of Chinese expert consensus on diagnosis of cardiogenic stroke 《Chinese Medical Journal》 SCIE CAS CSCD 2021年第5期505-507,共3页
Cardioembolic stroke(CES),also known as cardiogenic stroke,refers to a clinical syndrome caused by a cardiogenic embolus from the heart,leading to cerebral artery embolism through circulation,and it consequently resul... Cardioembolic stroke(CES),also known as cardiogenic stroke,refers to a clinical syndrome caused by a cardiogenic embolus from the heart,leading to cerebral artery embolism through circulation,and it consequently results in corresponding brain dysfunction.CES is associated with greater severity,poor outcomes,and a relatively high recurrence rate,compared with other subtypes of ischemic stroke. 展开更多
关键词 DIAGNOSIS cardio CLINICAL
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Chinese expert consensus statement for diagnosis and treatment of dementia with Lewy bodies 2020
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作者 Yong Ji Yan-Feng Li +2 位作者 dan-tao peng Zhi-Chao Chen Chinese Society of Geriatrics of Chinese Medical Association,Chinese Society of Microcirculation Neurodegenerative Diseases Committee 《Chinese Medical Journal》 SCIE CAS CSCD 2021年第21期2529-2531,共3页
Dementia with Lewy bodies(DLB)is the second most common type of neurodegenerative dementia,and prone to misdiagnosis and missed diagnosis in the clinic.Based on the evidence about DLB.
关键词 DIAGNOSIS STATEMENT TREATMENT
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