71. “我想我有多动症”:区分老年人迟发性多动症和轻度认知障碍

IF 3.8 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Anne Waniger , Maria Lapid
{"title":"71. “我想我有多动症”:区分老年人迟发性多动症和轻度认知障碍","authors":"Anne Waniger ,&nbsp;Maria Lapid","doi":"10.1016/j.jagp.2025.04.073","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Cognitive complaints in patients over the age of 65 are common and associated with underlying conditions such as depression, anxiety, or the early stages of a neurodegenerative disease. Patients meeting criteria for mild cognitive impairment (MCI) may also be misdiagnosed with attention deficit hyperactivity disorder (ADHD) due to overlapping symptoms such as difficulties with sustained attention, organization and memory. This overlap can complicate the differential diagnosis and may lead to inappropriate treatments. While studies have examined the increased risk of dementia in individuals with pre-existing ADHD, there is limited literature describing cases in which patients with a new late-onset ADHD diagnosis were later found to have a neurodegenerative disease as a better explanation for their symptoms. Accurate differentiation between MCI and ADHD is crucial for providing appropriate care and counseling for patients and their families.</div></div><div><h3>Methods</h3><div>We describe two cases of patients in their 70s who were initially diagnosed with ADHD after reporting subjective cognitive difficulties and undergoing neuropsychometric testing. Further evaluation, including neuroimaging, revealed cognitive impairment secondary to a neurodegenerative disease. We describe the clinical presentation, diagnostic workup, and the role of neuroimaging in clarifying the diagnosis.</div></div><div><h3>Results</h3><div>Patient #1 presented to a psychiatric clinic at age 75 with an 18-month history of word finding difficulties and depression, which had previously been in remission for several decades. Neuropsychometric testing one year prior to evaluation was normal across most domains, with relative areas of weakness with attention regulation and executive function, thought to be consistent with a diagnosis of ADHD with contributions from anxiety and depression. He was started on a new antidepressant in addition to Adderall. Repeat neuropsychometric testing did not indicate significant progression, and further testing was not pursued. One year later, he returned to his primary physician with worsening memory concerns and functional decline. He was evaluated by Neurology, who were concerned about cognitive impairment now in the moderate range. He underwent an FDG-PET, which demonstrated a pattern consistent with Alzheimer’s disease.</div><div>Patient #2 presented to a behavioral neurology clinic at age 77 for a second opinion regarding approximately 4 years of memory concerns. Neuropsychometric testing 6 months prior to evaluation revealed mild cognitive impairment with a mild decline in memory compared to previous testing 3.5 years earlier. He also underwent brain MRI and FDG-PET at that time, which were interpreted as normal. He was diagnosed with ADHD and started on Adderall. Subsequent neuropsychometric testing was consistent with MCI, amnestic, multi-domain. FDG-PET revealed mildly decreased FDG uptake in the left anteromedial temporal lobe and bilateral orbitofrontal regions, with an overall nonspecific pattern, though potentially related to limbic-predominant age-related TDP-43 encephalopathy. His amyloid PET was also positive, and he was found to have one copy of APOE e4. He was given the diagnosis of MCI due to a probable neurodegenerative disease and recommended to discontinue Adderall.</div></div><div><h3>Conclusions</h3><div>New-onset cognitive difficulties in older adults are unlikely to be due to ADHD and should prompt thorough evaluation for underlying neurodegenerative diseases or other cognitive disorders. Comprehensive assessment, including neuropsychometric testing, neuroimaging, and consistent follow-up, is essential to prevent misdiagnosis and the use of potentially inappropriate therapies such as psychostimulants.</div></div>","PeriodicalId":55534,"journal":{"name":"American Journal of Geriatric Psychiatry","volume":"33 10","pages":"Pages S52-S53"},"PeriodicalIF":3.8000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"71. \\\"I THINK I HAVE ADHD”: DIFFERENTIATING LATE-ONSET ADHD FROM MCI IN OLDER ADULTS\",\"authors\":\"Anne Waniger ,&nbsp;Maria Lapid\",\"doi\":\"10.1016/j.jagp.2025.04.073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Cognitive complaints in patients over the age of 65 are common and associated with underlying conditions such as depression, anxiety, or the early stages of a neurodegenerative disease. Patients meeting criteria for mild cognitive impairment (MCI) may also be misdiagnosed with attention deficit hyperactivity disorder (ADHD) due to overlapping symptoms such as difficulties with sustained attention, organization and memory. This overlap can complicate the differential diagnosis and may lead to inappropriate treatments. While studies have examined the increased risk of dementia in individuals with pre-existing ADHD, there is limited literature describing cases in which patients with a new late-onset ADHD diagnosis were later found to have a neurodegenerative disease as a better explanation for their symptoms. Accurate differentiation between MCI and ADHD is crucial for providing appropriate care and counseling for patients and their families.</div></div><div><h3>Methods</h3><div>We describe two cases of patients in their 70s who were initially diagnosed with ADHD after reporting subjective cognitive difficulties and undergoing neuropsychometric testing. Further evaluation, including neuroimaging, revealed cognitive impairment secondary to a neurodegenerative disease. We describe the clinical presentation, diagnostic workup, and the role of neuroimaging in clarifying the diagnosis.</div></div><div><h3>Results</h3><div>Patient #1 presented to a psychiatric clinic at age 75 with an 18-month history of word finding difficulties and depression, which had previously been in remission for several decades. Neuropsychometric testing one year prior to evaluation was normal across most domains, with relative areas of weakness with attention regulation and executive function, thought to be consistent with a diagnosis of ADHD with contributions from anxiety and depression. He was started on a new antidepressant in addition to Adderall. Repeat neuropsychometric testing did not indicate significant progression, and further testing was not pursued. One year later, he returned to his primary physician with worsening memory concerns and functional decline. He was evaluated by Neurology, who were concerned about cognitive impairment now in the moderate range. He underwent an FDG-PET, which demonstrated a pattern consistent with Alzheimer’s disease.</div><div>Patient #2 presented to a behavioral neurology clinic at age 77 for a second opinion regarding approximately 4 years of memory concerns. Neuropsychometric testing 6 months prior to evaluation revealed mild cognitive impairment with a mild decline in memory compared to previous testing 3.5 years earlier. He also underwent brain MRI and FDG-PET at that time, which were interpreted as normal. He was diagnosed with ADHD and started on Adderall. Subsequent neuropsychometric testing was consistent with MCI, amnestic, multi-domain. FDG-PET revealed mildly decreased FDG uptake in the left anteromedial temporal lobe and bilateral orbitofrontal regions, with an overall nonspecific pattern, though potentially related to limbic-predominant age-related TDP-43 encephalopathy. His amyloid PET was also positive, and he was found to have one copy of APOE e4. He was given the diagnosis of MCI due to a probable neurodegenerative disease and recommended to discontinue Adderall.</div></div><div><h3>Conclusions</h3><div>New-onset cognitive difficulties in older adults are unlikely to be due to ADHD and should prompt thorough evaluation for underlying neurodegenerative diseases or other cognitive disorders. Comprehensive assessment, including neuropsychometric testing, neuroimaging, and consistent follow-up, is essential to prevent misdiagnosis and the use of potentially inappropriate therapies such as psychostimulants.</div></div>\",\"PeriodicalId\":55534,\"journal\":{\"name\":\"American Journal of Geriatric Psychiatry\",\"volume\":\"33 10\",\"pages\":\"Pages S52-S53\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Geriatric Psychiatry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1064748125001836\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GERIATRICS & GERONTOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Geriatric Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1064748125001836","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

65岁以上患者的认知疾患很常见,并与潜在疾病如抑郁、焦虑或神经退行性疾病的早期阶段有关。符合轻度认知障碍(MCI)标准的患者也可能被误诊为注意缺陷多动障碍(ADHD),因为症状重叠,如持续注意力、组织和记忆困难。这种重叠会使鉴别诊断复杂化,并可能导致不适当的治疗。虽然有研究调查了先前患有多动症的人患痴呆症的风险增加,但关于新诊断为迟发性多动症的患者后来被发现患有神经退行性疾病以更好地解释其症状的案例,文献报道有限。准确区分轻度认知障碍和注意力缺陷多动症对于为患者及其家属提供适当的护理和咨询至关重要。方法我们描述了两例70多岁的患者,他们在报告主观认知困难并接受神经心理测试后最初被诊断为多动症。进一步的评估,包括神经影像学,显示继发于神经退行性疾病的认知障碍。我们描述临床表现,诊断检查,以及神经影像学在明确诊断中的作用。结果患者1在75岁时就诊于精神科诊所,有18个月的语言发现困难和抑郁史,之前已经缓解了几十年。评估前一年的神经心理测试在大多数领域都是正常的,相对而言,注意力调节和执行功能的薄弱区域被认为与ADHD的诊断一致,并与焦虑和抑郁有关。除了阿得拉,他还开始服用一种新的抗抑郁药。重复的神经心理测试没有显示明显的进展,也没有进行进一步的测试。一年后,他因记忆问题恶化和功能衰退而回到他的主治医生那里。神经病学对他进行了评估,他们担心他的认知障碍现在在中度范围内。他接受了FDG-PET检查,显示出与阿尔茨海默病一致的模式。患者2号在77岁时来到行为神经病学诊所,就大约4年的记忆问题征求第二意见。评估前6个月的神经心理测试显示,与3.5年前的前一次测试相比,轻度认知障碍和轻度记忆力下降。同时行脑MRI和FDG-PET检查,结果正常。他被诊断患有多动症,并开始服用阿得拉。随后的神经心理测试与轻度认知障碍,健忘症,多域一致。FDG- pet显示左侧前内侧颞叶和双侧眶额区FDG摄取轻度减少,总体呈非特异性模式,但可能与边缘显性年龄相关性TDP-43脑病有关。他的淀粉样PET也呈阳性,他被发现有一个APOE e4拷贝。由于一种可能的神经退行性疾病,他被诊断为轻度认知损伤,并建议停止服用阿得拉。结论:老年人新发认知困难不太可能是由于ADHD引起的,应该对潜在的神经退行性疾病或其他认知障碍进行彻底的评估。全面的评估,包括神经心理测试、神经成像和持续的随访,对于防止误诊和使用可能不适当的治疗方法(如精神兴奋剂)至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
71. "I THINK I HAVE ADHD”: DIFFERENTIATING LATE-ONSET ADHD FROM MCI IN OLDER ADULTS

Introduction

Cognitive complaints in patients over the age of 65 are common and associated with underlying conditions such as depression, anxiety, or the early stages of a neurodegenerative disease. Patients meeting criteria for mild cognitive impairment (MCI) may also be misdiagnosed with attention deficit hyperactivity disorder (ADHD) due to overlapping symptoms such as difficulties with sustained attention, organization and memory. This overlap can complicate the differential diagnosis and may lead to inappropriate treatments. While studies have examined the increased risk of dementia in individuals with pre-existing ADHD, there is limited literature describing cases in which patients with a new late-onset ADHD diagnosis were later found to have a neurodegenerative disease as a better explanation for their symptoms. Accurate differentiation between MCI and ADHD is crucial for providing appropriate care and counseling for patients and their families.

Methods

We describe two cases of patients in their 70s who were initially diagnosed with ADHD after reporting subjective cognitive difficulties and undergoing neuropsychometric testing. Further evaluation, including neuroimaging, revealed cognitive impairment secondary to a neurodegenerative disease. We describe the clinical presentation, diagnostic workup, and the role of neuroimaging in clarifying the diagnosis.

Results

Patient #1 presented to a psychiatric clinic at age 75 with an 18-month history of word finding difficulties and depression, which had previously been in remission for several decades. Neuropsychometric testing one year prior to evaluation was normal across most domains, with relative areas of weakness with attention regulation and executive function, thought to be consistent with a diagnosis of ADHD with contributions from anxiety and depression. He was started on a new antidepressant in addition to Adderall. Repeat neuropsychometric testing did not indicate significant progression, and further testing was not pursued. One year later, he returned to his primary physician with worsening memory concerns and functional decline. He was evaluated by Neurology, who were concerned about cognitive impairment now in the moderate range. He underwent an FDG-PET, which demonstrated a pattern consistent with Alzheimer’s disease.
Patient #2 presented to a behavioral neurology clinic at age 77 for a second opinion regarding approximately 4 years of memory concerns. Neuropsychometric testing 6 months prior to evaluation revealed mild cognitive impairment with a mild decline in memory compared to previous testing 3.5 years earlier. He also underwent brain MRI and FDG-PET at that time, which were interpreted as normal. He was diagnosed with ADHD and started on Adderall. Subsequent neuropsychometric testing was consistent with MCI, amnestic, multi-domain. FDG-PET revealed mildly decreased FDG uptake in the left anteromedial temporal lobe and bilateral orbitofrontal regions, with an overall nonspecific pattern, though potentially related to limbic-predominant age-related TDP-43 encephalopathy. His amyloid PET was also positive, and he was found to have one copy of APOE e4. He was given the diagnosis of MCI due to a probable neurodegenerative disease and recommended to discontinue Adderall.

Conclusions

New-onset cognitive difficulties in older adults are unlikely to be due to ADHD and should prompt thorough evaluation for underlying neurodegenerative diseases or other cognitive disorders. Comprehensive assessment, including neuropsychometric testing, neuroimaging, and consistent follow-up, is essential to prevent misdiagnosis and the use of potentially inappropriate therapies such as psychostimulants.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
13.00
自引率
4.20%
发文量
381
审稿时长
26 days
期刊介绍: The American Journal of Geriatric Psychiatry is the leading source of information in the rapidly evolving field of geriatric psychiatry. This esteemed journal features peer-reviewed articles covering topics such as the diagnosis and classification of psychiatric disorders in older adults, epidemiological and biological correlates of mental health in the elderly, and psychopharmacology and other somatic treatments. Published twelve times a year, the journal serves as an authoritative resource for professionals in the field.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信