{"title":"ARTS作为一种心脏代谢生物标志物,填补痴呆诊断和治疗方面的空白。","authors":"Timothy Daly, Bruno P. Imbimbo","doi":"10.1002/alz.70811","DOIUrl":null,"url":null,"abstract":"<p>Cerebral arteriolosclerosis is a form of small vessel disease characterized by the hardening and thickening of deep arterioles of the brain, and is commonly observed in conditions such as hypertension, diabetes, and dementia. In a diverse community sample, Fleischman et al. found that an in vivo magnetic resonance imaging-based classifier of arteriolosclerosis (shortened to ARTS), based on demographic data, white matter hyperintensity burden, and measures of diffusion tensor imaging fractional anisotropy, was a reliable marker for risk of mild cognitive impairment, dementia, and stroke.<span><sup>1</sup></span> Arteriolosclerosis is a pathogenic mechanism that serves not just as a marker, but also provides an upstream explanation of reductions in brain blood flow, infarcts, and downstream impacts on cognitive impairment.<span><sup>2</sup></span> In dementia research and clinical practice, ARTS could thus provide a polyvalent biomarker of cardiometabolic contributions to cognitive impairment due to underlying conditions such as hypertension and diabetes,<span><sup>3</sup></span> for example, alongside neurodegenerative biomarkers of amyloid beta (Aβ) and tau of Alzheimer's disease (AD) in both diagnostics and therapeutics.</p><p>Concerning diagnostics, in the absence of neurodegenerative pathologies such as AD, ARTS could be used to confirm the diagnosis of vascular dementia in cognitively impaired persons, which currently relies on gross measures of infarcts, white matter damage, and atrophy.<span><sup>4</sup></span> In the presence of AD neuropathology, ARTS could provide a quantifiable measure of cardiometabolic comorbidities that independently contribute to cognitive decline.<span><sup>5</sup></span> Indeed, Section 7.2 of the Alzheimer's Association 2024 revised criteria for the diagnosis of AD<span><sup>6</sup></span> discusses “Biomarkers of common non-AD copathologies” and recognizes that while there are multiple neuroimaging markers of cerebrovascular disease, none of them are specific, and there is no unified summary measure for vascular brain injury, creating diagnostic ambiguity. ARTS is a promising alternative to current imaging-based markers of cerebrovascular disease that provides a quantifiable measure that is also specific, mechanistic, and clinically relevant.</p><p>As a therapeutic example of ARTS’ application, take the example of autosomal dominant AD, for which Müller et al. found that World Health Organization–defined high levels of physical activity were associated with up to 15 years longer cognitive function, but not due to reduced global Aβ burden.<span><sup>7</sup></span> Cardiometabolic biomarkers such as ARTS could thus be used complementarily alongside neurodegenerative biomarkers to provide a mechanistic explanation of the positive impacts of physical activity on cognitive function. In clinical trials, such as those testing the therapeutic value of cardioprotective glucose-lowering drugs such as metformin<span><sup>8</sup></span> and semaglutide<span><sup>9</sup></span> in AD, a similar logic could be used: Cummings’ criterion of correlation between clinical efficacy and a biomarker in the same trial<span><sup>10</sup></span> could be used to establish that putative treatments are either disease modifying when ARTS is specific (e.g., ARTS in vascular dementia)—or meaningfully reduce comorbidities when ARTS is an independent contributor to worsened cognition (e.g., ARTS in AD).</p><p>To qualify as a reliable biomarker for detecting cardiometabolic contributions to cognitive decline, ARTS should be further developed to meet the core US Food and Drug Administration criteria for approval of a diagnostic test: analytical performance, clinical validation, and clinical utility. This would require demonstrating robust and reproducible measurement methods for ARTS, confirming its accuracy to detect <i>post mortem</i> arteriolosclerosis in well-characterized cohorts as suggested by the authors (p. 12,<span><sup>1</sup></span>), and building the evidence base that its use would inform clinical decision making and/or improve patient outcomes.</p><p>Dr. Timothy Daly has no conflicts of interest to declare. Dr. Bruno P. Imbimbo is an employee at Chiesi Farmaceutici. He is listed as an inventor in a number of Chiesi Farmaceutici's patents for anti-Alzheimer's disease drugs. All author disclosures are in the supporting information.</p>","PeriodicalId":7471,"journal":{"name":"Alzheimer's & Dementia","volume":"21 10","pages":""},"PeriodicalIF":11.1000,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12538623/pdf/","citationCount":"0","resultStr":"{\"title\":\"ARTS as a cardiometabolic biomarker to bridge gaps in dementia diagnostics and therapeutics\",\"authors\":\"Timothy Daly, Bruno P. Imbimbo\",\"doi\":\"10.1002/alz.70811\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Cerebral arteriolosclerosis is a form of small vessel disease characterized by the hardening and thickening of deep arterioles of the brain, and is commonly observed in conditions such as hypertension, diabetes, and dementia. In a diverse community sample, Fleischman et al. found that an in vivo magnetic resonance imaging-based classifier of arteriolosclerosis (shortened to ARTS), based on demographic data, white matter hyperintensity burden, and measures of diffusion tensor imaging fractional anisotropy, was a reliable marker for risk of mild cognitive impairment, dementia, and stroke.<span><sup>1</sup></span> Arteriolosclerosis is a pathogenic mechanism that serves not just as a marker, but also provides an upstream explanation of reductions in brain blood flow, infarcts, and downstream impacts on cognitive impairment.<span><sup>2</sup></span> In dementia research and clinical practice, ARTS could thus provide a polyvalent biomarker of cardiometabolic contributions to cognitive impairment due to underlying conditions such as hypertension and diabetes,<span><sup>3</sup></span> for example, alongside neurodegenerative biomarkers of amyloid beta (Aβ) and tau of Alzheimer's disease (AD) in both diagnostics and therapeutics.</p><p>Concerning diagnostics, in the absence of neurodegenerative pathologies such as AD, ARTS could be used to confirm the diagnosis of vascular dementia in cognitively impaired persons, which currently relies on gross measures of infarcts, white matter damage, and atrophy.<span><sup>4</sup></span> In the presence of AD neuropathology, ARTS could provide a quantifiable measure of cardiometabolic comorbidities that independently contribute to cognitive decline.<span><sup>5</sup></span> Indeed, Section 7.2 of the Alzheimer's Association 2024 revised criteria for the diagnosis of AD<span><sup>6</sup></span> discusses “Biomarkers of common non-AD copathologies” and recognizes that while there are multiple neuroimaging markers of cerebrovascular disease, none of them are specific, and there is no unified summary measure for vascular brain injury, creating diagnostic ambiguity. ARTS is a promising alternative to current imaging-based markers of cerebrovascular disease that provides a quantifiable measure that is also specific, mechanistic, and clinically relevant.</p><p>As a therapeutic example of ARTS’ application, take the example of autosomal dominant AD, for which Müller et al. found that World Health Organization–defined high levels of physical activity were associated with up to 15 years longer cognitive function, but not due to reduced global Aβ burden.<span><sup>7</sup></span> Cardiometabolic biomarkers such as ARTS could thus be used complementarily alongside neurodegenerative biomarkers to provide a mechanistic explanation of the positive impacts of physical activity on cognitive function. In clinical trials, such as those testing the therapeutic value of cardioprotective glucose-lowering drugs such as metformin<span><sup>8</sup></span> and semaglutide<span><sup>9</sup></span> in AD, a similar logic could be used: Cummings’ criterion of correlation between clinical efficacy and a biomarker in the same trial<span><sup>10</sup></span> could be used to establish that putative treatments are either disease modifying when ARTS is specific (e.g., ARTS in vascular dementia)—or meaningfully reduce comorbidities when ARTS is an independent contributor to worsened cognition (e.g., ARTS in AD).</p><p>To qualify as a reliable biomarker for detecting cardiometabolic contributions to cognitive decline, ARTS should be further developed to meet the core US Food and Drug Administration criteria for approval of a diagnostic test: analytical performance, clinical validation, and clinical utility. This would require demonstrating robust and reproducible measurement methods for ARTS, confirming its accuracy to detect <i>post mortem</i> arteriolosclerosis in well-characterized cohorts as suggested by the authors (p. 12,<span><sup>1</sup></span>), and building the evidence base that its use would inform clinical decision making and/or improve patient outcomes.</p><p>Dr. Timothy Daly has no conflicts of interest to declare. Dr. Bruno P. Imbimbo is an employee at Chiesi Farmaceutici. He is listed as an inventor in a number of Chiesi Farmaceutici's patents for anti-Alzheimer's disease drugs. 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引用次数: 0
摘要
脑小动脉硬化是一种以脑深部小动脉硬化和增厚为特征的小血管疾病,常见于高血压、糖尿病和痴呆等病症。在不同的社区样本中,Fleischman等人发现,基于人口统计数据、白质高强度负荷和弥散张量成像分数各向异性的体内磁共振成像小动脉硬化分类器(简称ARTS)是轻度认知障碍、痴呆和中风风险的可靠标志小动脉硬化是一种致病机制,它不仅是一种标志物,而且还为脑血流量减少、梗死和对认知障碍的下游影响提供了上游解释因此,在痴呆症研究和临床实践中,ARTS可以提供一种多价生物标志物,用于诊断和治疗阿尔茨海默病(AD)的淀粉样蛋白β (a β)和tau神经退行性生物标志物,以及高血压和糖尿病等潜在疾病导致的认知障碍的心脏代谢贡献。在诊断方面,在没有AD等神经退行性病理的情况下,ARTS可用于确认认知障碍者血管性痴呆的诊断,目前这依赖于梗死、白质损伤和萎缩的总体测量在存在AD神经病理学的情况下,ARTS可以提供一种可量化的衡量独立导致认知能力下降的心脏代谢合并症的方法事实上,阿尔茨海默病协会2024年修订的AD6诊断标准第7.2节讨论了“常见非ad病理的生物标志物”,并认识到虽然脑血管疾病有多种神经影像学标志物,但它们都不是特异性的,而且对于血管性脑损伤也没有统一的总结测量,造成了诊断的模糊性。ARTS是目前基于成像的脑血管疾病标志物的一种有希望的替代方法,它提供了一种可量化的测量方法,也具有特异性、机械性和临床相关性。作为ARTS应用的一个治疗例子,以常染色体显性AD为例,m勒等人发现,世界卫生组织定义的高水平体育活动与长达15年的认知功能延长有关,但不是由于全球a β负担的减少因此,ARTS等心脏代谢生物标志物可以与神经退行性生物标志物互补使用,为体育活动对认知功能的积极影响提供机制解释。在临床试验中,例如测试心脏保护降糖药物(如二甲双胍和semaglutide)对AD的治疗价值,可以使用类似的逻辑:在同一试验中,Cummings的临床疗效与生物标志物之间的相关性标准10可用于确定,当ARTS具有特异性时(例如,ARTS治疗血管性痴呆),假定的治疗方法可以改善疾病,或者当ARTS是认知恶化的独立因素时(例如,AD中的ARTS),可显著减少合并症。为了有资格作为检测心脏代谢对认知能力下降的贡献的可靠生物标志物,应进一步发展ARTS,以满足美国食品和药物管理局批准诊断测试的核心标准:分析性能、临床验证和临床实用性。这将需要证明ARTS的可靠和可重复的测量方法,确认其在作者建议的特征明确的队列中检测死后小动脉硬化的准确性(第12,1页),并建立证据基础,证明其使用将为临床决策提供信息和/或改善患者预后。蒂莫西·戴利没有利益冲突需要申报。Bruno P. Imbimbo博士是Chiesi制药公司的员工。他是Chiesi制药公司多项抗阿尔茨海默病药物专利的发明人。所有作者披露的信息都在支持信息中。
ARTS as a cardiometabolic biomarker to bridge gaps in dementia diagnostics and therapeutics
Cerebral arteriolosclerosis is a form of small vessel disease characterized by the hardening and thickening of deep arterioles of the brain, and is commonly observed in conditions such as hypertension, diabetes, and dementia. In a diverse community sample, Fleischman et al. found that an in vivo magnetic resonance imaging-based classifier of arteriolosclerosis (shortened to ARTS), based on demographic data, white matter hyperintensity burden, and measures of diffusion tensor imaging fractional anisotropy, was a reliable marker for risk of mild cognitive impairment, dementia, and stroke.1 Arteriolosclerosis is a pathogenic mechanism that serves not just as a marker, but also provides an upstream explanation of reductions in brain blood flow, infarcts, and downstream impacts on cognitive impairment.2 In dementia research and clinical practice, ARTS could thus provide a polyvalent biomarker of cardiometabolic contributions to cognitive impairment due to underlying conditions such as hypertension and diabetes,3 for example, alongside neurodegenerative biomarkers of amyloid beta (Aβ) and tau of Alzheimer's disease (AD) in both diagnostics and therapeutics.
Concerning diagnostics, in the absence of neurodegenerative pathologies such as AD, ARTS could be used to confirm the diagnosis of vascular dementia in cognitively impaired persons, which currently relies on gross measures of infarcts, white matter damage, and atrophy.4 In the presence of AD neuropathology, ARTS could provide a quantifiable measure of cardiometabolic comorbidities that independently contribute to cognitive decline.5 Indeed, Section 7.2 of the Alzheimer's Association 2024 revised criteria for the diagnosis of AD6 discusses “Biomarkers of common non-AD copathologies” and recognizes that while there are multiple neuroimaging markers of cerebrovascular disease, none of them are specific, and there is no unified summary measure for vascular brain injury, creating diagnostic ambiguity. ARTS is a promising alternative to current imaging-based markers of cerebrovascular disease that provides a quantifiable measure that is also specific, mechanistic, and clinically relevant.
As a therapeutic example of ARTS’ application, take the example of autosomal dominant AD, for which Müller et al. found that World Health Organization–defined high levels of physical activity were associated with up to 15 years longer cognitive function, but not due to reduced global Aβ burden.7 Cardiometabolic biomarkers such as ARTS could thus be used complementarily alongside neurodegenerative biomarkers to provide a mechanistic explanation of the positive impacts of physical activity on cognitive function. In clinical trials, such as those testing the therapeutic value of cardioprotective glucose-lowering drugs such as metformin8 and semaglutide9 in AD, a similar logic could be used: Cummings’ criterion of correlation between clinical efficacy and a biomarker in the same trial10 could be used to establish that putative treatments are either disease modifying when ARTS is specific (e.g., ARTS in vascular dementia)—or meaningfully reduce comorbidities when ARTS is an independent contributor to worsened cognition (e.g., ARTS in AD).
To qualify as a reliable biomarker for detecting cardiometabolic contributions to cognitive decline, ARTS should be further developed to meet the core US Food and Drug Administration criteria for approval of a diagnostic test: analytical performance, clinical validation, and clinical utility. This would require demonstrating robust and reproducible measurement methods for ARTS, confirming its accuracy to detect post mortem arteriolosclerosis in well-characterized cohorts as suggested by the authors (p. 12,1), and building the evidence base that its use would inform clinical decision making and/or improve patient outcomes.
Dr. Timothy Daly has no conflicts of interest to declare. Dr. Bruno P. Imbimbo is an employee at Chiesi Farmaceutici. He is listed as an inventor in a number of Chiesi Farmaceutici's patents for anti-Alzheimer's disease drugs. All author disclosures are in the supporting information.
期刊介绍:
Alzheimer's & Dementia is a peer-reviewed journal that aims to bridge knowledge gaps in dementia research by covering the entire spectrum, from basic science to clinical trials to social and behavioral investigations. It provides a platform for rapid communication of new findings and ideas, optimal translation of research into practical applications, increasing knowledge across diverse disciplines for early detection, diagnosis, and intervention, and identifying promising new research directions. In July 2008, Alzheimer's & Dementia was accepted for indexing by MEDLINE, recognizing its scientific merit and contribution to Alzheimer's research.