ArticlebioRxiv : the preprint server for biology2026
Synergistic and redundant information dynamics are modulated by Alzheimer's disease and cognitive impairment.
Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Background: The early diagnosis of Alzheimer's disease (AD), a cause of progressive cognitive decline, remains challenging. Recent information-theoretic advances allow brain dynamics to be quantified in terms of how regions share and combine information. Integrated Information Decomposition (ΦID) separates redundant (the same content present in multiple regions) from synergistic information (new content that emerges only when regions are considered together). Such information-dynamic measures may provide biomarkers relevant to AD risk and progression. Methods: Here we applied integrated information decomposition (ΦID) to resting-state fMRI from the Alzheimer's Disease Neuroimaging Initiative (ADNI), to test whether ΦID measures are diagnostically sensitive and track cognition along the AD spectrum. For each region, we computed total synergy and redundancy and compared values across cognitively normal (CN), mild cognitive impairment (MCI), and AD groups. Results: Compared to CN, AD patients showed a striking synergy reduction across the entire brain, in concert with widespread redundancy increases, particularly in the executive and default mode networks. Transitions from CN to AD included an intermediate MCI decrease in redundancy, possibly reflecting early disease compensation strategies. This AD informational shift from complex higher level information processing to more robust inefficient forms likely reflects a cognitive shift to simpler, less integrative cognitive processes. Indeed, when re-analysing the data according to a standard cognitive clinical test (the Montreal Cognitive Assessment), we found a synergy-redundancy shift in high versus low performers broadly very similar to the CN to AD shift. Conclusion: AD shows a clear information-processing signature: reduced global synergy and increased redundancy, especially in the executive control network. These striking results provide powerful insights into the widespread information processing reconfiguration that occurs in AD, with clear changes already emerging at the earlier MCI stage. Further, these results provide a novel route to support early diagnosis and stratification.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.