{"title":"血管内皮生长因子是血管性痴呆症而非阿尔茨海默病的有效生物标志物:荟萃分析","authors":"Ling-Zhi Xu, Fang-Yu Li, Jin Xu, Bing-Qiu Li, Ying Li, Jian-Ping Jia","doi":"10.1002/dad2.12612","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Vascular pathology is known to contribute to dementia and vascular endothelial growth factor (VEGF) is a well-established biomarker associated with vascular alterations. Nonetheless, research findings on VEGF in Alzheimer's disease (AD) and vascular dementia (VaD) are inconsistent across various studies.</p><p><strong>Methods: </strong>We conducted a meta-analysis to elucidate relationships between VEGF and AD/VaD.</p><p><strong>Results: </strong>Twenty-four studies were included. Pooled data showed that both blood and cerebrospinal fluid (CSF) VEGF levels were higher in VaD patients, whereas no significant difference was found between AD patients and healthy controls. However, the correlation between blood VEGF and AD was found among studies with AD pathology verification. And blood VEGF levels were higher in AD patients than controls in \"age difference < 5 years\" subgroup and CSF samples for European cohorts.</p><p><strong>Discussion: </strong>This study highlights that VEGF is more effective for the diagnosis of VaD and vascular factors are also an important contributor in AD.</p><p><strong>Highlights: </strong>Vascular endothelial growth factor (VEGF) levels were higher in the vascular dementia group, but not in the overall Alzheimer's disease (AD) group.Correlation between VEGF and AD was found among studies with clear AD pathological verification.Elevated VEGF in the cerebrospinal fluid might be a diagnostic marker for AD in European populations.</p>","PeriodicalId":53226,"journal":{"name":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","volume":"16 2","pages":"e12612"},"PeriodicalIF":4.0000,"publicationDate":"2024-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11193096/pdf/","citationCount":"0","resultStr":"{\"title\":\"Vascular endothelial growth factor is an effective biomarker for vascular dementia, not for Alzheimer's disease: A meta-analysis.\",\"authors\":\"Ling-Zhi Xu, Fang-Yu Li, Jin Xu, Bing-Qiu Li, Ying Li, Jian-Ping Jia\",\"doi\":\"10.1002/dad2.12612\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Vascular pathology is known to contribute to dementia and vascular endothelial growth factor (VEGF) is a well-established biomarker associated with vascular alterations. Nonetheless, research findings on VEGF in Alzheimer's disease (AD) and vascular dementia (VaD) are inconsistent across various studies.</p><p><strong>Methods: </strong>We conducted a meta-analysis to elucidate relationships between VEGF and AD/VaD.</p><p><strong>Results: </strong>Twenty-four studies were included. Pooled data showed that both blood and cerebrospinal fluid (CSF) VEGF levels were higher in VaD patients, whereas no significant difference was found between AD patients and healthy controls. However, the correlation between blood VEGF and AD was found among studies with AD pathology verification. And blood VEGF levels were higher in AD patients than controls in \\\"age difference < 5 years\\\" subgroup and CSF samples for European cohorts.</p><p><strong>Discussion: </strong>This study highlights that VEGF is more effective for the diagnosis of VaD and vascular factors are also an important contributor in AD.</p><p><strong>Highlights: </strong>Vascular endothelial growth factor (VEGF) levels were higher in the vascular dementia group, but not in the overall Alzheimer's disease (AD) group.Correlation between VEGF and AD was found among studies with clear AD pathological verification.Elevated VEGF in the cerebrospinal fluid might be a diagnostic marker for AD in European populations.</p>\",\"PeriodicalId\":53226,\"journal\":{\"name\":\"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring\",\"volume\":\"16 2\",\"pages\":\"e12612\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-06-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11193096/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/dad2.12612\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/4/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/dad2.12612","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/4/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
简介众所周知,血管病理学是导致痴呆症的原因之一,而血管内皮生长因子(VEGF)是一种与血管改变相关的公认生物标志物。然而,不同研究对阿尔茨海默病(AD)和血管性痴呆(VaD)中血管内皮生长因子的研究结果并不一致:我们进行了一项荟萃分析,以阐明 VEGF 与 AD/VaD 之间的关系:结果:共纳入 24 项研究。汇总数据显示,VaD 患者血液和脑脊液(CSF)中的 VEGF 水平均较高,而 AD 患者与健康对照组之间无明显差异。然而,在进行 AD 病理学验证的研究中发现,血液 VEGF 与 AD 之间存在相关性。在 "年龄差异讨论 "中,AD 患者的血液 VEGF 水平高于对照组:本研究强调血管内皮生长因子对 VaD 的诊断更有效,血管因子也是导致 AD 的重要因素:血管内皮生长因子(VEGF)水平在血管性痴呆组中较高,但在整个阿尔茨海默病(AD)组中并不高.在有明确AD病理验证的研究中发现了VEGF与AD之间的相关性.在欧洲人群中,脑脊液中升高的VEGF可能是AD的诊断标志物.
Vascular endothelial growth factor is an effective biomarker for vascular dementia, not for Alzheimer's disease: A meta-analysis.
Introduction: Vascular pathology is known to contribute to dementia and vascular endothelial growth factor (VEGF) is a well-established biomarker associated with vascular alterations. Nonetheless, research findings on VEGF in Alzheimer's disease (AD) and vascular dementia (VaD) are inconsistent across various studies.
Methods: We conducted a meta-analysis to elucidate relationships between VEGF and AD/VaD.
Results: Twenty-four studies were included. Pooled data showed that both blood and cerebrospinal fluid (CSF) VEGF levels were higher in VaD patients, whereas no significant difference was found between AD patients and healthy controls. However, the correlation between blood VEGF and AD was found among studies with AD pathology verification. And blood VEGF levels were higher in AD patients than controls in "age difference < 5 years" subgroup and CSF samples for European cohorts.
Discussion: This study highlights that VEGF is more effective for the diagnosis of VaD and vascular factors are also an important contributor in AD.
Highlights: Vascular endothelial growth factor (VEGF) levels were higher in the vascular dementia group, but not in the overall Alzheimer's disease (AD) group.Correlation between VEGF and AD was found among studies with clear AD pathological verification.Elevated VEGF in the cerebrospinal fluid might be a diagnostic marker for AD in European populations.
期刊介绍:
Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.