Each study has a usefulness score out of 100 (rubric version 4.0). Tap a score to see what makes it up.
Highest usefulness score first. Studies without a score come last.
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In APOE4/4 homozygotes receiving 150mg BID tramiprosate, efficacy in the traditional Mild AD patients (MMSE 20-26) was higher than the overall group (MMSE 16-26) and efficacy in the Mild patients (MMSE 22-26) was highest.
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Four-week changes in NPI-Q total scores did not differ significantly between the treatment and placebo groups.
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Mild cognitive impairment (MCI) in Parkinson's disease (PD) may be associated with subtle functional impairment and worse quality of life.
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76/100
Statin therapy was not associated with cognitive impairment in RCTs.
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In patients without baseline cognitive dysfunction, short-term data are most compatible with no adverse effect of statins on cognition, and long-term data may support a beneficial role for statins in the prevention of dementia.
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Antibody administration was well tolerated with doses up to 400 mg weekly.
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76/100
Letters16 October 2007Adjusted-Dose Warfarin versus Aspirin for Preventing Stroke in Patients with Atrial FibrillationRobert G. The study's important results indicate that the relative efficacy and safety of warfarin for stroke prevention can be extended to very elderly patients who are managed by nonspecialists.
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Cholinergic dysfunction is also associated with neuropsychiatric and functional deficits, but results from randomized controlled trials of cholinesterase inhibitors are conflicting.
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In a randomized, placebo-controlled, double-blind study, we investigated whether statins alter cholesterol metabolites and reduce Abeta levels in the cerebrospinal fluid of 44 patients with Alzheimer's disease.
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Donanemab-mediated slowing of disease progression occurred across baseline tau PET and plasma P-tau217 levels.
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75/100
There were 132 846 individuals (mean [SD] age, 80.4 [7.6] years; 61.8% women; mean [SD] body mass index [BMI], 25.5 [4.6]) with a diagnosis of dementia included in cohort 1, 159 419 individuals (mean [SD] age, 81.2 [7.6] years; 59.7% women; mean [SD] body mass index [BMI], 25.6 [4.7]) with a diagnosis of dementia included in cohort 2, and 92 328 individuals with a diagnosis of dementia included in cohort 3 (mean [SD] age, 80.9 [7.7] years; 58.5% women; mean [SD] body mass index [BMI], 25.5 [4.7]).
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75/100
BDNF levels did not change significantly and were not associated with improvement in overall neuropsychiatric symptoms or in cognitive function.
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A total of 1795 participants were enrolled (lecanemab:898; placebo:897).
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Participants in the placebo group displayed cognitive and functional decline, whereas lithium-treated patients remained stable over 2 years.
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The safety profile was similar for 20 μg treatment and placebo patients.
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Short term (26 weeks) tideglusib was acceptably safe but produced no clinical benefit in this trial.
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PBT2 is a copper/zinc ionophore that rapidly restores cognition in mouse models of Alzheimer's disease (AD).
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72 patients with PDD or DLB were randomly assigned and started treatment: 34 with memantine and 38 with placebo. 56 (78%) completed the study.
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Inclusion criteria were early AD (mini-mental state examination [MMSE] score between 20 and 26 points or Alzheimer's disease assessment scale-cognitive subscale (ADAS-cog) score between 10 and 25 points), taking a stable dose of acetylcholinesterase inhibitor (donepezil, galantamine, or rivastigmine) for at least 4 months, a modified Hachinski score of 4 points or less, and CT or MRI results that were consistent with AD.
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Twenty-five out of 44 completed the trial.
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No difference was seen in Clinical Global Impression scores between patients receiving placebo and those receiving linopirdine (n = 189).
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Treatment with GLP-1 RAs may provide a new opportunity to reduce the incidence of dementia in patients with type 2 diabetes.
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Pooled evidence from available trials reporting both reduction in amyloid levels and change in cognition suggests that amyloid reduction strategies do not substantially improve cognition.
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Based on integrated review of laboratory, electrocardiogram, adverse events, and MRI, AAB-003 was safe and well tolerated up to 8 mg/kg for up to 91 weeks (FIH and extension trials) in patients with mild to moderate AD.
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Diabetes and hyperinsulinemia may be risk factors for Alzheimer's disease (AD).
From across this topic
10 of the 902 studies in this topic, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 10. The same 10 appear here every time.
- Benzodiazepine use and hip fractures in the elderly: who is at greatest risk?
- Representativeness of Participants Eligible to Be Enrolled in Clinical Trials of Aducanumab for Alzheimer Disease Compared With Medicare Beneficiaries With Alzheimer Disease and Mild Cognitive Impairment
- GLP-1 Receptor Agonists vs SGLT2 Inhibitors for Alzheimer’s Disease Risk in Type 2 Diabetes: A Systematic Review and Meta-Analysis
- Nefiracetam. Daiichi Seiyaku
- Efficacy and adverse effects of cholinesterase inhibitors and memantine in vascular dementia: a meta-analysis of randomised controlled trials
- Randomized controlled trial of standardized Bacopa monniera extract in age-associated memory impairment
- Galantamine: a randomized, double-blind, dose comparison in patients with Alzheimer's disease
- Benzodiazepines of long and short elimination half-life and the risk of hip fracture
- Cholinesterase as a Target for Drug Development in Alzheimer's Disease
- The Course of Psychopathologic Features in Mild to Moderate Alzheimer Disease