Dementia, a progressive neurodegenerative disorder affecting memory, cognition, and behaviour, poses a major global health challenge in aging populations. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies →
Original source
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Recent studies highlight the significance of plasma phosphorylated tau proteins, neurofilament light chain, and amyloid-beta ratios as reliable biomarkers. 4 key findings →
Evidence: low
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Parameters such as clinical status, GCA scale, MTA scale, Fazekas scale, strategic infarction, Koedam score, stroke, hypertension, diabetes mellitus, dyslipidemia, and cardiovascular disease do not have significant correlations with MoCA-INA scores. 4 key findings →
Evidence: low
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There was a significant correlation in MoCA and FLCI-2 measures but no significant correlation between the language measures (CIUs, FLCI-2, or word count). 3 key findings →
Evidence: low
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Researchers tested whether a tablet-based cognitive test (TabCAT) could substitute for traditional paper-and-pencil memory tests in people with early-onset Alzheimer's. Scores on the tablet's attention/executive tasks correlated strongly (above 0.7) with standard tests like the MMSE and MoCA, and one subtest could distinguish people with amyloid plaques from those without with good accuracy (AUC 0.82). 5 key findings →
Design: cross-sectional
Participants: 475
Evidence: moderate
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Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-08-19
The Dementia Trials Accelerator (DTA) is a UK-wide programme designed to improve the feasibility, efficiency, and inclusiveness of recruitment into clinical trials of dementia and related brain-health conditions. 5 key findings →
Participants: 10,000
Evidence: low
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Original source
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-08-22
Using the ADNI dataset, we found that the model realigned patients according to their clinical diagnoses. 1 key finding →
Design: longitudinal study
Evidence: moderate
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-08-27
Early identification of cognitive impairment remains challenging in settings where comprehensive cognitive and clinical assessments are not available. 1 key finding →
Evidence: low
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Original source
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-09-07
The Middle East and North Africa (MENA) region is projected to experience the fastest growth in dementia burden globally, yet population-based data on cognitive aging remain scarce. 1 key finding →
Participants: 3,027
Evidence: low
Full summary, score breakdown and related studies →
Original source
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-09-11
INTRODUCTIONIndividuals with Alzheimers disease (AD) exhibit substantial heterogeneity in the severity of vascular changes and neurodegeneration, making the identification of biologically meaningful subtypes across the AD spectrum critical for improving prognosis and tailoring interventions. 1 key finding →
Design: longitudinal study
Participants: 1,396
Evidence: moderate
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Original source
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-09-12
These findings show that model-based, adaptive assessments can support high-frequency, remote detection and scalable longitudinal monitoring of early memory decline, providing a new way to assess memory decline trajectories in healthy aging and dementia. 3 key findings →
Design: longitudinal study
Participants: 24
Evidence: moderate
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-09-23
For TabCAT tests, there were no notable floor or ceiling effects, and test scores were associated with age and education as expected. 3 key findings →
Design: cohort study
Participants: 563
Evidence: moderate
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Original source
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-09-23
ObjectiveTo investigate whether a lifetime history of DSM-5 AUD and correlated indices of alcohol consumption are associated with accelerated age-related cognitive decline in middle-aged and older adults. 5 key findings →
Design: cross-sectional
Participants: 1,421
Evidence: moderate
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Original source
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv (preprint)
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2026-09-25
MTD showed excellent discrimination of CU versus MCI/DEM (AUC=.89; 95% CI=.87-.92), and discriminability remained high for CU versus MCI (AUC=.88; 95% CI=.85-.92). 5 key findings →
Design: cohort study
Participants: 1,224
Evidence: moderate
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16/100
⚠ Report — not peer-reviewed
alzhub usefulness score 16 out of 100.
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2013-05-22
Evidence: low
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16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-10-28
Sociodemographic and clinical variables routinely recorded in PC EHRs may contribute to dementia identification. 3 key findings →
Design: cross-sectional
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Preprints.org
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2026-10-26
Evidence for interventions that reduce refusal is strongest for music during personal care and modified bathing methods, with some support for positive communication and person-centred approaches, though quality is generally low and few studies involve family caregivers in community settings. 5 key findings →
Design: narrative review
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-10-07
Symptom chronology emerged as a robust diagnostic discriminator, underscoring the clinical value of temporal disease trajectories. 3 key findings →
Participants: 932
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-09-18
Alzheimer’s disease (AD) is a neurodegenerative disorder that is characterized by structural changes of the hippocampus, thus hippocampal morphology becomes an important biomarker for early diagnosis. 2 key findings →
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-09-14
Implementation of an EHR-enabled AD care pathway was associated with improved adoption of guideline-concordant cognitive assessment and recommended diagnostic evaluation in primary care across three health systems. 5 key findings →
Participants: 10,206
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-09-07
Dementia public stigma was associated with education, dementia knowledge, media exposure, chronic diseases, and contact experience with people living with dementia. 5 key findings →
Design: cross-sectional
Participants: 3,055
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-08-27
Individuals with MCI and AD exhibit marked deficits in the performance and accuracy of upper-limb reaching and catching movements when assessed in a VR environment. 3 key findings →
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Research Square
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2026-08-20
Medication adherence in older adults was strongly influenced by cognitive impairment, gender, health literacy and cohabitation. 4 key findings →
Design: cross-sectional
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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Preprints.org
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2026-08-03
Apathy and depression are among the most common neuropsychiatric symptoms in dementia. 5 key findings →
Design: narrative review
Evidence: low
Full summary, score breakdown and related studies →
Original source
16/100
⚠ Preprint — not yet peer-reviewed
alzhub usefulness score 16 out of 100.
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medRxiv
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2026-08-03
Multimodal integration of cognitive, neuroimaging, and polygenic data in the MHS-RWD tool yields strong discrimination for both early diagnosis of dementia and AD differential diagnosis. 2 key findings →
Participants: 1,100
Evidence: low
Full summary, score breakdown and related studies →
Original source
How the 0–100 score works — and why some entries are capped
This is alzhub's own score. It is not an official metric, not an impact factor,
and no journal, publisher or ranking body endorses it. We built it so that a reader who is not a
scientist can tell a landmark trial from a conference abstract without having to already know the
difference. Every point comes from one of 20 components, all of them printed on the study itself,
so you can disagree with our arithmetic rather than having to trust the total.
- Journal tier up to 10 pts
- Journal's citation record up to 4 pts
- Study design up to 12 pts
- Strength of evidence up to 5 pts
- Peer-review validation up to 10 pts
- How recent up to 5 pts
- Sample size up to 4 pts
- Effect reported up to 3 pts
- Studied in people up to 3 pts
- Randomised / blinded up to 2 pts
- Times cited up to 7 pts
- Citations per year up to 5 pts
- Impact for its field and year up to 6 pts
- Cited by studies here up to 6 pts
- Still being cited up to 4 pts
- Senior author's track record up to 4 pts
- Institution's track record up to 3 pts
- Multi-centre collaboration up to 3 pts
- Indexed in PubMed up to 2 pts
- Free to read up to 2 pts
Journals are placed in ordered tiers, never given a numeric impact factor — we
could not verify current impact factors from a source we control, and an invented one would be
worse than none. Tier 1 is the top-tier general journals (NEJM, The Lancet, JAMA, Nature, Science,
Nature Medicine); tier 2 is the leading specialty journals; tier 3 is every other peer-reviewed
journal. A separate part scores how much the journal's own papers are cited, which tells the
tier-3 journals apart.
Two rules we don't bend. First, we never fill in a
missing value: if a record does not state a sample size or a design, that component scores
zero, and if we simply have no data for a part, such as a citation count, that part is left out and
the study is scored on the parts we could check. The study card says which. Second, anything that is not a peer-reviewed
article is capped at 16/100 and carries a warning chip — so a conference abstract or
a company press release can never outrank a peer-reviewed paper, no matter how good it looks.
We rank a rigorous null result — a good trial showing that something does not
work — above an early positive finding. Someone deciding whether to buy a supplement is served by
that, and the rigour is already counted by the design and journal components.
The score is computed from the published data alone and is
reproducible: the same file always yields the same numbers.
See the whole rubric drawn out →
— four charts covering all 28,580 studies: how the scores are spread and where the cap
bites, which of the 20 components the library is strong and weak on, which subjects rest on
stronger evidence, and what kinds of study each subject is actually built from.