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Alzheimer Disease And Associated Disorders[JOURNAL]

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More Publications Needed on Cognitively Impaired-Not MCI: Call for Papers.

Luchsinger JA

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42257557 · Publisher ↗

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CHMP2B p.Ala30Ser Variant in Biomarker-Confirmed Early-Onset Alzheimer Disease: A Potential Endolysosomal Disease Modifier.

Totuk O

Alzheimer Dis Assoc Disord · 2026 Jun · PMID 42246690 · Publisher ↗

Endolysosomal dysfunction has been increasingly implicated in the pathogenesis of neurodegenerative diseases. The charged multivesicular body protein 2B (CHMP2B) gene encodes a component of the endosomal sorting complexe... Endolysosomal dysfunction has been increasingly implicated in the pathogenesis of neurodegenerative diseases. The charged multivesicular body protein 2B (CHMP2B) gene encodes a component of the endosomal sorting complexes required for transport (ESCRT-III), which regulates endosomal trafficking, multivesicular body formation, and autophagosome-lysosome fusion. Mutations in CHMP2B are classically associated with autosomal dominant frontotemporal dementia. Here, we report a 59-year-old woman with biomarker-confirmed Alzheimer disease (AD) (A+T+N+) carrying a heterozygous CHMP2B c.90C>T (p.Ala30Ser) variant identified by targeted exome sequencing after negative testing for APP, APOE, PSEN1, and PSEN2. The patient presented with progressive episodic memory impairment and spatial disorientation over 3 years. Brain MRI showed prominent posterior cortical atrophy, and cerebrospinal fluid biomarkers demonstrated decreased Aβ42 and elevated phosphorylated and total tau levels consistent with AD pathology. Dysfunction of CHMP2B-mediated endolysosomal pathways may impair intracellular protein degradation and influence tau clearance mechanisms. This observation suggests that rare variants in endolysosomal pathway genes may contribute to AD pathophysiology.

Early Gut Microbiome Alterations in Mild Cognitive Impairment Reflect Changes in Alzheimer Disease.

Brandt E, Koivisto A, Pereira P … +7 more , Mustanoja E, Auvinen P, Saari T, Rusanen M, Leinonen V, Scheperjans F, Kärkkäinen V

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42228448 · Full text

INTRODUCTION: Alterations in the gut-brain axis have been increasingly linked to neurodegenerative diseases, including Alzheimer disease (AD). It remains unclear whether these microbiome changes are already present durin... INTRODUCTION: Alterations in the gut-brain axis have been increasingly linked to neurodegenerative diseases, including Alzheimer disease (AD). It remains unclear whether these microbiome changes are already present during early cognitive decline. We examined whether gut microbiome alterations characteristic of AD are detectable in mild cognitive impairment (MCI) and whether these changes follow a similar pattern across the cognitive continuum. METHODS: This case-control study included 78 participants: 37 cognitively healthy controls, 20 individuals with MCI, and 21 individuals with prodromal or mild AD. Cognitive performance was assessed using the CERAD neuropsychological battery, and disease severity was assessed using the Clinical Dementia Rating. Dietary data were collected, and fecal samples were analyzed using 16S rRNA gene amplicon sequencing. RESULTS: We identified 16 bacterial genera associated with cognitive status. Genera such as Lacticaseibacillus , Raoultella , and Buttiauxella were reduced in AD, with similar decreases already evident in MCI. In contrast, Anaerovorax and an unclassified Comamonadaceae genus were increased in AD. Several alterations showed a consistent trend from normal cognition through MCI to AD. DISCUSSION: Gut microbiome alterations characteristic of AD appear already present in early cognitive decline and follow a similar pattern in MCI. These findings support the potential of microbiome profiles as early, noninvasive biomarkers of AD.

Improvements in Cogstate Test Performance Depend on Number and Frequency of Prior Tests: Evidence from a Randomized Follow-Up Design.

Murchland AR, Chen R, Blacker D … +3 more , Kang JH, Glymour MM, Haneuse S

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42224199 · Publisher ↗

OBJECTIVES: Practice effects (PEs), improvements in cognitive test performance with repeated exposure, must be addressed in longitudinal studies of cognitive aging. Although many cognitive assessments are marketed as rob... OBJECTIVES: Practice effects (PEs), improvements in cognitive test performance with repeated exposure, must be addressed in longitudinal studies of cognitive aging. Although many cognitive assessments are marketed as robust to PEs, evidence is limited. Randomizing testing features enables direct quantification of PEs but remains underutilized. METHODS: Among Nurses' Health Study II participants (N=14,802), we examined PEs in the Cogstate Brief Battery arising from increased testing repetition and frequency using conditionally randomized 6- or 12-month regimens (2014 to 2019). RESULTS: Taking the assessment twice previously, compared with once previously, at the 12-month assessment (defined as frequency PEs) was associated with 0.13 SD-higher global cognitive scores (95% CI: 0.10-0.16), corresponding to between-person age differences of 4.3 to 6.8 years. Taking the second assessment 6-months compared with 12-months after baseline (defined as frequency of PEs) was associated with 0.04 SD-higher global cognitive scores ( P <0.01), corresponding to between-person 1.3 to 1.6-year age differences. Repetition and frequency PEs both appeared to be greater in magnitude for participants who were older at baseline, but uncertainty was high in formal tests of effect modification. CONCLUSIONS: Over short follow-up periods, repetition PEs may obscure age-related cognitive decline using Cogstate. Randomizing testing features can be used to strengthen cognitive aging research.

Identification of Functional lncRNAs in Alzheimer Disease by Integrative Analysis of lncRNA-mRNA Network Based on Competing Endogenous RNA Mechanism.

Su Y, Ren H, Huang S … +1 more , Hao Y

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42224107 · Publisher ↗

BACKGROUND: Emerging evidence highlights the critical involvement of noncoding RNAs (ncRNAs) in the pathologic process of Alzheimer disease (AD). However, the precise functional contributions and regulatory landscapes of... BACKGROUND: Emerging evidence highlights the critical involvement of noncoding RNAs (ncRNAs) in the pathologic process of Alzheimer disease (AD). However, the precise functional contributions and regulatory landscapes of long noncoding RNAs (lncRNAs) in AD remain unclear. OBJECTIVE: This study aims to delineate the regulatory roles of functional lncRNAs in AD by systematically analyzing lncRNA-mRNA interactions within an AD-associated network, leveraging the competing endogenous RNA (ceRNA) framework. METHODS: We constructed an AD-specific lncRNA-mRNA network by integrating a probe reannotation pipeline with experimentally validated microRNA (miRNA)-lncRNA/mRNA interactions. Key lncRNAs were identified through topological analysis, while bidirectional hierarchical clustering was applied to define functional modules. Pearson correlation coefficients were computed to assess the association patterns of lncRNA-mRNA pairs. RESULTS: Using a structured analytical approach, we identified 31 differentially expressed lncRNAs and 1045 mRNAs within the AD network. Topological analysis revealed SNHG12, MIR17HG, and GAS5 as central regulatory nodes, indicating their potential roles in network stability and transcriptional regulation. A functionally coherent module of lncRNA-mRNA interactions was identified through clustering, with enrichment in multiple AD-relevant signaling pathways, including neuroinflammation and synaptic dysfunction, suggesting a mechanistic role for lncRNAs in disease-associated processes. Furthermore, leveraging the ceRNA model, we mapped dysregulated ceRNA interactions, uncovering significant alterations in ceRNA crosstalk between AD and non-AD conditions, which may reflect broader disruptions in posttranscriptional gene regulation. CONCLUSIONS: Our findings provide key insights into the functional architecture of lncRNA regulatory networks in AD, offering a refined perspective on their contributions to disease pathology and highlighting potential biomarkers and therapeutic targets.

Valacyclovir Treatment in Mild Cognitive Impairment: The VALMCI Randomized Clinical Trial.

Devanand DP, Huey ED, Qian M … +11 more , Wei R, Motter JN, Nedic L, Andrews HF, Deliyannides DA, Maayan L, Graff J, Deehan E, Acosta EP, Zanderigo F, Goldberg TE

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42210804 · Publisher ↗

BACKGROUND: Evidence from neuroscience, epidemiology, and electronic health records studies implicates herpes simplex viruses (HSV) as potentially etiologic for Alzheimer disease (AD). METHODS: The VALMCI study was condu... BACKGROUND: Evidence from neuroscience, epidemiology, and electronic health records studies implicates herpes simplex viruses (HSV) as potentially etiologic for Alzheimer disease (AD). METHODS: The VALMCI study was conducted in a research outpatient clinic specializing in memory disorders. The efficacy and side effects of valacyclovir 4 g/day were compared with placebo in a 12-month pilot, randomized, double-blind trial of participants with mild cognitive impairment (MCI), seropositivity to HSV1 or HSV2, and positive 18 F-florbetapir PET scan. RESULTS: Totally, 42 of 50 participants (84%) completed the trial. In linear mixed-effects model analyses with age, sex, and apolipoprotein E e4 genotype as covariates, change in the primary outcome of 18 F-florbetapir PET mean SUVR was not significant with least-squares mean difference -0.01 (95% CI: -0.12 to 0.10; P =0.82). For secondary cognitive and functional outcomes, PACC composite z -score showed the least square mean difference 0.16 (95% CI: -0.17 to 0.49; P =0.32), and ADCS-ADL-PI score showed the least square mean difference 1.96 (95% CI: -0.43 to 4.34; P =0.11). CONCLUSION: The results do not support the use of valacyclovir in the treatment of individuals with MCI with HSV seropositivity and PET amyloid positivity.

Gut Microbiome Differences Between Early Alzheimer Disease and Idiopathic Normal Pressure Hydrocephalus.

Brandt E, Koivisto A, Pereira P … +7 more , Mustanoja E, Auvinen P, Saari T, Rusanen M, Leinonen V, Scheperjans F, Kärkkäinen V

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42206504 · Full text

BACKGROUND: Alzheimer disease (AD) and idiopathic normal pressure hydrocephalus (iNPH) are neurodegenerative diseases causing memory decline. Previous studies have demonstrated an altered gut microbiome (GM) in both cond... BACKGROUND: Alzheimer disease (AD) and idiopathic normal pressure hydrocephalus (iNPH) are neurodegenerative diseases causing memory decline. Previous studies have demonstrated an altered gut microbiome (GM) in both conditions. In this study, we compared the GM composition between the groups to find out how if the GM composition differed between the cognitively healthy individuals (CO) and AD groups, as well as between the AD and iNPH groups. METHODS: Thirty-seven CO participants, 21 mild AD patients and 10 participants with shunted iNPH gave fecal samples, which were subjected to 16S amplicon sequencing. Then, genus-level differences were analyzed. Information about comorbidities and diet was collected, and cognitive function was evaluated. RESULTS: Compared with the CO group, Anaerovorax and an unknown genus of the Comamonadaceae family increased, whereas Enterobacter, Absicoccus, Buttiauxella, Raoultella , and Lacticaseibacillus decreased in the AD group. Compared with the iNPH group, Paramuribaculum , an unknown genus of the Desulfovibrionaceae family, Ruficoccus and Mitsuokella increased, whereas Anaeromassilibacillus and Desulfovibrio decreased in the AD group. CONCLUSIONS: We demonstrated differences in the GM composition between the AD and CO groups, as well as between the AD and iNPH groups. To our knowledge, this is the first report to compare the 2 neurodegenerative diseases and demonstrate GM differences.

Validity of the Montreal Cognitive Assessment-Basic (MoCA-B) in a Dutch Memory Clinic.

Kessels RPC, van Bergen FS, Vogel CMA … +3 more , Smarius M, Pouwels IS, Dautzenberg PD

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42206499 · Full text

People with low educational levels or low literacy skills tend to obtain lower scores on cognitive screens, even in the absence of cognitive impairments, possibly resulting in false positive diagnoses. The Montreal Cogni... People with low educational levels or low literacy skills tend to obtain lower scores on cognitive screens, even in the absence of cognitive impairments, possibly resulting in false positive diagnoses. The Montreal Cognitive Assessment-Basic (MoCA-B) has been developed to overcome this, but studies so far are limited to low-income countries. This study examined the MoCA-B [total score and Memory Index Score (MIS)] in a European memory clinic context. Fifty-five controls, 37 patients with mild cognitive impairment and 47 dementia patients were included. Results showed that a MoCA-B total cutoff score <25 is valid for distinguishing controls from MCI or dementia patients. The MoCA-B MIS showed an acceptable diagnostic accuracy for controls versus MCI (<12) and controls versus dementia (<11). No valid cutoff score could be established for MCI versus dementia patients. Our findings show that the MoCA-B can also be validly applied in a European memory clinic setting.

Serum Lipoprotein Subclasses as Predictors of Tensor-Based Morphometry Atrophy in the Alzheimer Disease Continuum: A Brief Report.

Khosravi F, Ashrafi M, Abroushan D … +12 more , Ramezannezhad E, Niaki SRP, Radmanesh M, Haratian A, Taki A, Nekahi N, Moshiri Y, Rahimi M, Fadavian H, Mousavi SM, Fard AM, Alzheimer’s Disease Neuroimaging Initiative (ADNI)

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42200516 · Publisher ↗

OBJECTIVE: To evaluate whether serum lipoprotein subclasses and related metabolites quantified by nuclear magnetic resonance (NMR) are associated with longitudinal tensor-based morphometry (TBM) atrophy in mild cognitive... OBJECTIVE: To evaluate whether serum lipoprotein subclasses and related metabolites quantified by nuclear magnetic resonance (NMR) are associated with longitudinal tensor-based morphometry (TBM) atrophy in mild cognitive impairment (MCI). METHODS: Secondary analysis of ADNI-GO and ADNI-2 participants with a baseline diagnosis of MCI, baseline serum Nightingale NMR metabolomics, and at least 2 quality-controlled T1-weighted MRI examinations processed with the Mayo TBM-SyN pipeline. The TBM-SyN summary score was the mean annualized log-Jacobian volume change across 31 Alzheimer disease (AD)-vulnerable regions, derived from baseline-to-follow-up symmetric registration. Linear mixed-effects models adjusted for age and included subject-level random intercepts. Associations with the Clinical Dementia Rating (CDR) and the Alzheimer Disease Assessment Scale (ADAS) were tested. RESULTS: The analytic cohort included 93 participants (mean age: 65.23 y, SD: 6.47; 51 male, 54.8%). Eight biomarkers were significantly associated with TBM-SyN atrophy: medium HDL free cholesterol percentage (M_HDL_FC_PCT; β =-0.0020, P =0.0016), apolipoprotein B ( P =0.005), apolipoprotein A1 ( P =0.017), extra-large HDL particle concentration (XL_HDL_P; P =0.029), medium HDL particle concentration ( P =0.028), medium HDL cholesterol ( P =0.025), medium HDL cholesterol esters ( P =0.031), and glycerol ( P =0.038). XL_HDL_P alone was associated with the CDR score ( P =0.03). CONCLUSIONS: Specific HDL-related lipoprotein subclasses, apolipoproteins, and glycerol are associated with TBM-derived structural atrophy in MCI, supporting peripheral lipid metabolism as a candidate scalable correlate of early neurodegeneration.

Olfaction, Cognition, and Early Signs of Neurodegenerative Disease in a Community-Based Sample of Older Adults.

Jacobsen E, Zhang Y, Ganguli M … +5 more , Chang CH, Kamboh MI, Karikari TK, Berman SB, Snitz BE

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42189736 · Publisher ↗

INTRODUCTION: We investigated associations of impaired odor identification with signs of early Alzheimer disease (AD) and Lewy Body disease (LBD). METHODS: In 787 community-sampled adults aged ≥65 without dementia or Par... INTRODUCTION: We investigated associations of impaired odor identification with signs of early Alzheimer disease (AD) and Lewy Body disease (LBD). METHODS: In 787 community-sampled adults aged ≥65 without dementia or Parkinson disease, we evaluated cross-sectional associations of olfaction (Brief Smell Identification Test, BSIT) with 5 cognitive domain scores, gait, tone, tremor, REM sleep behavior disorder (RBD) symptoms, and plasma biomarkers of neurodegeneration. RESULTS: In adjusted regression models, worse BSIT scores were associated with lower cognitive scores in all domains, slowed gait, resting tremor, and RBD-like symptoms. The association between BSIT and memory was stronger in APOE4 carriers. In cognitively unimpaired participants (Clinical Dementia Rating=0), most associations remained significant. BSIT scores were associated with plasma p-tau217 and NfL in exploratory analyses. CONCLUSION: Odor identification is associated with cognition in an undifferentiated pattern and with Parkinsonian signs in older adults, even among those with normal cognition. The stronger association in APOE4 carriers potentially suggests an emerging AD-like pathway, consistent with exploratory plasma biomarker analyses. In sum, evidence points to olfactory dysfunction as relevant for both AD and LBD-associated future risk.

New Friendships and Cognitive Functions in a Dementia Prevention Program for Community-Dwelling Older Japanese Adults.

Shimizu K, Yamashita M, Sakurai H … +10 more , Yamashiro D, Kuroda Y, Sugimoto T, Matsumoto N, Uchida K, Yokoyama Y, Onoyama A, Suzuki H, Fujiwara Y, Sakurai T

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42188536 · Publisher ↗

OBJECTIVE: To investigate the association between cognitive changes and new friendship formation among older adults in a multidomain dementia prevention program. METHODS: A 1-year multidomain intervention was conducted f... OBJECTIVE: To investigate the association between cognitive changes and new friendship formation among older adults in a multidomain dementia prevention program. METHODS: A 1-year multidomain intervention was conducted for 34 community-dwelling older adults (18 females, 16 males, mean age 78.3 y, SD=4.3) meeting the operational criteria for mild cognitive impairment. Cognitive changes were evaluated using the Montreal Cognitive Assessment (MoCA-J). Participants reported new friendships based on social support functions (eg, emotional and instrumental support). A 2-way repeated-measures ANCOVA (time×group), adjusted for education, examined the main effects and interactions on the total MoCA-J and subscale scores. RESULTS: The total MoCA-J scores showed no significant main effects or interaction. However, subscale analysis revealed a significant main effect of time on visuospatial/executive function and a significant main effect of friend-presence group on orientation. Specifically, the friend-presence group consistently exhibited higher orientation scores than the absence group at both time points. CONCLUSION: Overall, cognitive function was maintained throughout the program. Exploratory findings suggest that visuospatial/executive functions showed potential improvement, and preserved orientation was associated with successful friendship formation. Thus, facilitating social connections alongside standard activities may enhance future dementia prevention programs.

Pupillometry as a Differential Indicator of Cognitive Processing in Alzheimer Disease and Behavioral Variant Frontotemporal Dementia.

El Haj M, Boutoleau-Bretonnière C, Moustafa A … +1 more , Chapelet G

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42184234 · Publisher ↗

INTRODUCTION: While extensive research has explored cognitive processing with pupillometry in the general population, limited attention has been given to its application in neurodegenerative diseases. This study, for the... INTRODUCTION: While extensive research has explored cognitive processing with pupillometry in the general population, limited attention has been given to its application in neurodegenerative diseases. This study, for the first time, investigates general cognitive processing using pupillometry in both Alzheimer disease (AD) and behavioral variant frontotemporal dementia (bvFTD). METHODS: Pupil diameter was monitored in patients with AD, patients with bvFTD, and control participants under 2 conditions. The first condition involved subtraction (ie, subtracting 9 from 100 and continuing to subtract to a total of 5 subtractions). The second control condition involved counting aloud from 1. RESULTS: Analysis demonstrated increased pupil diameters during subtraction than during counting in patients with bvFTD, patients with AD, and control participants. During both counting and subtraction, smaller pupil diameters were observed in patients with bvFTD compared with patients with AD and in patients with AD compared with control participants. CONCLUSIONS: These findings indicate that pupil size can effectively reflect the cognitive load intensity in patients with bvFTD and patients with AD, suggesting the potential of pupillometry as a differential indicator of cognitive processing in neurodegenerative diseases.

Detecting Cognitive Impairment Early in Hispanic and Black Older Adults: Community Voices From South Central Texas.

Hilsabeck RC, Santiago-Mejias S, Fletcher TL … +5 more , Rhodes SL, Maestre GE, Seshadri S, Patel NK, Epps FR

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42184217 · Publisher ↗

BACKGROUND: Alzheimer disease and related dementias (ADRD) are more prevalent in Black and Hispanic older adults and are also more likely to be undetected and misdiagnosed. The purpose of this study was to engage with Bl... BACKGROUND: Alzheimer disease and related dementias (ADRD) are more prevalent in Black and Hispanic older adults and are also more likely to be undetected and misdiagnosed. The purpose of this study was to engage with Black and Hispanic communities about interest in and support needed for memory screening. METHODS: Participants were recruited from established community partners of the South Texas Alzheimer's Disease Research Center to engagein a 90-minute listening session. The session was recorded with participants' permission, and a thematic analysis was conducted by 2 independent coders. RESULTS: Sixteen individuals (81% female, 88% Hispanic or Black) from various perspectives participated (eg, health care workers, persons with dementia, caregivers). Four core themes emerged: building trust, access and time barriers, community-specific literature, and representative messengers. Trust was noted to be foundational, encompassing who delivers the screening and where it takes place. Transportation, time burden, competing caregiving responsibilities, work schedules, and limited access to technology/internet were key barriers. The need to create accessible and relatable literature and videos tailored to diverse educational levels and cultural backgrounds was also emphasized. CONCLUSIONS: Trusted members of the community could be accepted to perform memory screenings and provide education. Partnering with faith-based organizations, senior centers, and other community hubs would help overcome barriers to screening.

Depression and Anxiety in Stroke-Related and Alzheimer Disease-Related Pseudobulbar Affect: A TriNetX Retrospective Cohort Study.

Dereschuk KJ, Asay CC, Espiridion ED

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42138134 · Publisher ↗

INTRODUCTION: Pseudobulbar affect (PBA) is a disorder of emotional expression associated with neurological diseases, including stroke and Alzheimer disease. Depression and anxiety frequently co-occur, but whether psychia... INTRODUCTION: Pseudobulbar affect (PBA) is a disorder of emotional expression associated with neurological diseases, including stroke and Alzheimer disease. Depression and anxiety frequently co-occur, but whether psychiatric outcomes differ by neurological etiology remains unclear. OBJECTIVE: To compare the risk and timing of depressive episodes and anxiety disorders in stroke-associated versus Alzheimer disease-associated PBA. METHODS: We conducted a retrospective cohort study using the TriNetX Global Health Research Network (2020 to 2025). Two mutually exclusive cohorts were identified: PBA with stroke and PBA with Alzheimer disease. Outcomes were depressive episode (ICD-10-CM F32) and anxiety disorder, unspecified (ICD-10-CM F41.9), occurring after PBA diagnosis. One-to-one propensity score matching was performed for age, sex, race, and ethnicity. Kaplan-Meier analyses and Cox proportional hazards models assessed risk and timing. RESULTS: After matching, 1074 patients per cohort were included for depression analysis. Depression occurred in 68.7% of Alzheimer disease-PBA versus 34.7% of stroke-PBA (absolute risk difference 34.0%, P <0.001; HR=2.52, 95% CI: 2.22-2.86). For anxiety (n=946 per cohort), rates were 48.8% versus 24.9% (absolute risk difference 23.9%, P <0.001; HR=1.98, 95% CI: 1.70-2.30). CONCLUSION: Alzheimer disease-associated PBA confers a higher and earlier risk of depression and anxiety, supporting enhanced psychiatric screening in neurodegenerative disease.

Cognitive and Neuroanatomical Effects of Fatty Acid Amide Hydrolase Polymorphism rs324420 in Aging and Alzheimer Disease.

Mori-Fegan DK, Wong YY, Noor S … +5 more , Wu CY, Ryoo S, Mielnik C, Ross RA, Swardfager W

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42127232 · Publisher ↗

INTRODUCTION: Therapeutic options for Alzheimer disease (AD) are limited. Modulating the endocannabinoid system through fatty acid amide hydrolase (FAAH) is a promising target. We investigated how the FAAH functional pol... INTRODUCTION: Therapeutic options for Alzheimer disease (AD) are limited. Modulating the endocannabinoid system through fatty acid amide hydrolase (FAAH) is a promising target. We investigated how the FAAH functional polymorphism rs324420 influences cognition and brain structure across the AD continuum, particularly in interaction with amyloid (Aβ) pathology. METHODS: One thousand, five hundred seven Alzheimer Disease Neuroimaging Initiative participants were analyzed [631 cognitively normal (CN); 876 AD/Mild Cognitive Impairment (ADMCI)]. Cross-sectional and 48-month longitudinal models assessed interactions between rs324420 minor-allele carrier status and Aβ-positivity [(18F)-Florbetapir PET SUVR>1.11] on cognitive tests and regional brain volumes as judged by MRI. RESULTS: Cross-sectionally, CN and Aβ-positive CN carriers demonstrated better executive function than noncarriers. Aβ-positive ADMCI carriers showed greater baseline episodic memory, while Aβ-negative carriers had larger inferior temporal and nucleus accumbens volumes compared with noncarriers. Longitudinally, Aβ-positive CN carriers showed slower whole-brain atrophy. Whole-ADMCI carriers exhibited significantly slower declines in global cognition and language. Aβ-positive ADMCI carriers showed preserved anterior cingulate, fusiform gyrus, and nucleus accumbens volumes. Aβ-negative ADMCI carriers had greater atrophy in the inferior temporal and nucleus accumbens regions. DISCUSSION: Neuroprotective effects of rs324420 (lowered FAAH activity) appear contingent on cerebral Aβ-positivity, specifically preserving brain volume and slowing cognitive decline longitudinally. Findings support biomarker-informed precision approaches for endocannabinoid-targeted interventions in AD and aging.

Risk of Alzheimer Disease and Other Dementias in Patients With Parkinson Disease: A Nationwide Cohort Study.

Bae Y, Kim M, Jeon SR … +2 more , Lee SW, Jung H

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 42084241 · Publisher ↗

INTRODUCTION: Dementia is a major nonmotor complication of Parkinson disease (PD), yet its subtype-specific and time-dependent risk remains incompletely characterized. METHODS: We conducted a nationwide retrospective coh... INTRODUCTION: Dementia is a major nonmotor complication of Parkinson disease (PD), yet its subtype-specific and time-dependent risk remains incompletely characterized. METHODS: We conducted a nationwide retrospective cohort study using Korean National Health Insurance claims and health screening data. Newly diagnosed PD patients (ICD-10: G20) and propensity score-matched controls were followed after a 3-year washout period. Dementia outcomes were defined using ICD-10 codes and classified as Alzheimer disease dementia (F00, G30), other dementias (F01-F03), and overall dementia. Incidence rate ratios (IRRs) and adjusted hazard ratios (aHRs) were estimated using Cox models. RESULTS: PD was associated with higher dementia incidence across all subtypes. IRRs were 3.38 (95% CI: 3.12-3.67) for Alzheimer disease dementia, 4.67 (95% CI: 4.16-5.23) for other dementias, and 3.60 (95% CI: 3.33-3.90) for overall dementia. Elevated risks persisted after multivariable adjustment and were more pronounced in younger patients and men, with variation by dementia subtype and time since diagnosis. CONCLUSIONS: PD was associated with an increased risk of dementia in this nationwide cohort. The heterogeneity observed by subtype, age, and follow-up period suggests that dementia risk may emerge early in specific subgroups, supporting early cognitive monitoring without implying causality.

Survey of Mobile Phone Usage Among Patients With Cognitive Impairment.

Suzumura S, Suzuki M, Maeda A … +6 more , Okaniwa K, Okochi Y, Kondo H, Tanabe S, Takechi H, Otaka Y

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 41972298 · Publisher ↗

Mobile phones are increasingly being proposed as tools to support daily life among older adults with cognitive impairment; however, empirical data on their actual ownership and use in clinical settings remain limited. Th... Mobile phones are increasingly being proposed as tools to support daily life among older adults with cognitive impairment; however, empirical data on their actual ownership and use in clinical settings remain limited. This study aimed to clarify mobile phone ownership and usage patterns among older adults with cognitive impairment attending memory clinics. Eighty-two older adults with cognitive impairment (mean age: 80.4 y; mean Mini-Mental State Examination score: 18.1 points) were included. Data were collected using caregiver-administered questionnaires and analyzed descriptively. Among the participants, 65 (79.3%) owned a mobile phone, with an almost equal distribution of smartphones (n=33) and featured phones (n=32). Fifteen phone owners did not use their devices. Reported use was largely limited to basic communication functions. These findings indicate limited mobile phone ownership and functional use among older adults with cognitive impairment and underscore the need to consider cognitive limitations when implementing mobile technologies.

Association Between Engagement and Agitation in Dementia: Clinical and Environmental Factors in Nonpharmacological Therapy.

Nishitani A, Tanaka H

Alzheimer Dis Assoc Disord · 2026 Apr-Jun 01 · PMID 41909921 · Publisher ↗

INTRODUCTION: Agitation is a common behavioral symptom in dementia that increases caregiver burden and contributes to hospitalization or institutionalization. Nonpharmacological interventions are essential to manage agit... INTRODUCTION: Agitation is a common behavioral symptom in dementia that increases caregiver burden and contributes to hospitalization or institutionalization. Nonpharmacological interventions are essential to manage agitation; however, their effectiveness has been inconsistent. A potential explanation is that engagement-defined as patients' attitudes and behaviors during therapy-has rarely been incorporated into the evaluation of these interventions. This study aimed to clarify the association between engagement and agitation and to identify related clinical and environmental factors. METHODS: This cross-sectional study included 66 hospitalized individuals with dementia (mean age 81.4±6.9 y). Assessments comprised demographics, cognitive function, activities of daily living, behavioral and psychological symptoms, environmental parameters, comorbidities, pain, and engagement. Correlation and multiple regression analyses were conducted to explore factors associated with engagement. RESULTS: Engagement was positively correlated with cognitive function and daily living abilities, and negatively correlated with dementia severity, pain, agitation, depression, visual impairment, and humidity. Multiple regression analysis showed engagement was independently associated with pain, dementia severity, visual impairment, and agitation. CONCLUSIONS: Engagement in dementia was influenced by pain, dementia severity, visual impairment, and agitation. Attention to these factors, particularly pain management, may optimize nonpharmacological interventions, enhance engagement, and help reduce agitation in dementia.

Lecanemab and Donanemab Combination Therapy for Alzheimer's Disease-The Cocktail May Work Even Better Together.

Dinnerstein E

Alzheimer Dis Assoc Disord · 2026 Jan-Mar 01 · PMID 41773886 · Publisher ↗

Lecanemab and Donanemab are two new FDA-approved antiamyloid immunotherapies that are Alzheimer disease modifying agents. They do not work on the same target, however. While Lecanemab targets pathologic amyloid protofibr... Lecanemab and Donanemab are two new FDA-approved antiamyloid immunotherapies that are Alzheimer disease modifying agents. They do not work on the same target, however. While Lecanemab targets pathologic amyloid protofibrils, Donanemab targets the amyloid plaque itself intracranially. In theory, they can be administered together, as combination therapy, to produce an augmented effect. Research of the feasibility of such a combination will require bringing together competing pharmaceutical companies, which can only happen by setting a national agenda bringing together academia, pharma, the government and advocacy groups.

Assessing Language Impairments Across the Neurodegeneration Continuum: Diagnostic Utility of the BECLA-TR in MCI and Alzheimer Disease.

Tosun S, Karali FS, Eskioğlu Eİ … +2 more , Çinar N, Macoir J

Alzheimer Dis Assoc Disord · 2026 Jan-Mar 01 · PMID 41773885 · Publisher ↗

BACKGROUND: As the global population ages, the prevalence of major neurocognitive disorders (MND), particularly Alzheimer disease (AD), continues to rise. Mild Cognitive Impairment (MCI) is considered a prodromal stage o... BACKGROUND: As the global population ages, the prevalence of major neurocognitive disorders (MND), particularly Alzheimer disease (AD), continues to rise. Mild Cognitive Impairment (MCI) is considered a prodromal stage of AD, yet differentiating MCI from early-stage AD remains a clinical challenge, especially regarding language impairments. OBJECTIVE: This study aimed to examine the diagnostic utility of the Turkish adaptation of the Batterie d'Évaluation Cognitive du Langage (BECLA-Tr) and to determine its effectiveness as one of the first multidimensional language assessments standardized for Turkish speakers. METHODS: Ninety participants (30 MCI, 30 AD, and 30 healthy controls) completed the BECLA-Tr in addition to general cognitive and language screening tests. The BECLA-Tr assesses 4 domains: recognition of spoken and written words, semantic processing, spoken production, and written language. RESULTS: AD participants showed significant impairments across nearly all BECLA-Tr domains compared with both MCI and controls. MCI participants exhibited selective deficits in semantic processing while maintaining comparable performance to controls in spoken and written production. CONCLUSION: The BECLA-Tr demonstrated strong diagnostic sensitivity for detecting language impairments across the neurodegeneration continuum, supporting its clinical use for early detection and intervention in MCI and AD.
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