# 15 years of longitudinal genetic, clinical, cognitive, imaging, and biochemical measures in DIAN

**Authors:** Alisha J. Daniels, Eric McDade, Jorge J. Llibre-Guerra, Chengjie Xiong, Richard J. Perrin, Laura Ibanez, Charlene Supnet-Bell, Carlos Cruchaga, Alison Goate, Alan E. Renton, Tammie L. S. Benzinger, Brian A. Gordon, Jason Hassenstab, Celeste Karch, Allan Levey, John C. Morris, Virginia Buckles, Ricardo F. Allegri, Patricio Chrem, Sarah B. Berman, Jasmeer P. Chhatwal, Martin R. Farlow, Nick C. Fox, Gregory S. Day, Takeshi Ikeuchi, Mathias Jucker, Johannes Levin, Jae-Hong Lee, David Aguillon, Leonel Takada, Ana Luisa Sosa, Ralph Martins, Hiroshi Mori, James M. Noble, Stephen Salloway, Edward Huey, Raquel Sánchez-Valle, Peter R. Schofield, Jee Hoon Roh, Randall J. Bateman, Alisha J. Daniels, Alisha J. Daniels, Eric McDade, Jorge J. Llibre-Guerra, Chengjie Xiong, Richard J. Perrin, Laura Ibanez, Charlene Supnet-Bell, Carlos Cruchaga, Alison Goate, Alan E. Renton, Brian A. Gordon, Jason Hassenstab, Celeste Karch, Allan Levey, John C. Morris, Virginia Buckles, Ricardo F. Allegri, Patricio Chrem, Sarah B. Berman, Jasmeer P. Chhatwal, Martin R. Farlow, Nick C. Fox, Gregory S. Day, Takeshi Ikeuchi, Mathias Jucker, Johannes Levin, Jae-Hong Lee, David Aguillon, Leonel Takada, Ana Luisa Sosa, Ralph Martins, Hiroshi Mori, James M. Noble, Stephen Salloway, Edward Huey, Raquel Sánchez-Valle, Peter R. Schofield, Jee Hoon Roh, Randall J. Bateman, Tammie L. S. Benzinger, David M. Holtzman, Anne M. Fagan, Erin Franklin, Xiong Xu, Ruijin Lu, Guoqiao Wang, Yan Li, Emily Gremminger, Laura Courtney, Gina Jerome, Elizabeth Herries, Jennifer Stauber, Bryce Baker, Matthew Minton, Danielle M. Picarello, Russ Hornbeck, Allison Chen, Charles Chen, Shaney Flores, Nelly Joseph-Mathurin, Steve Jarman, Kelley Jackson, Sarah Keefe, Deborah Koudelis, Parinaz Massoumzadeh, Austin McCullough, Nicole McKay, Joyce Nicklaus, Christine Pulizos, Qing Wang, Edita Sabaredzovic, Hunter Smith, Jalen Scott, Ashlee Simmons, Jacqueline Rizzo, Jennifer Sullivan, Sarah Stout, Andrew J. Aschenbrenner, Jacob Marsh, Nicolas Barthelemy, Jinbin Xu, Erik C. B. Johnson, Nicholas T. Seyfried, Ezequiel Surace, Silvia Vazquez, Snezana Ikonomovic, Neelesh K. Nadkarni, David M. Cash, Natalie S. Ryan, Neill R. Graff-Radford, Kensaku Kasuga, Christoph Laske, Anna Hofmann, Elke Kuder-Buletta, Susanne Graber-Sultan, Ulrike Obermueller, Yvonne Roedenbeck, Jonathan Voglein, Francisco Lopera, Yudy Milena, Laura Ramirez, William S. Brooks, Jacob A. Bechara, Yoshiki Niimi, Pedro Rosa-Neto, John Ringman, Colin Masters

PMC · DOI: 10.1038/s44400-025-00047-7 · 2026-02-16

## TL;DR

The DIAN study tracks brain aging and Alzheimer's disease in families with a genetic risk over 15 years, providing a detailed dataset for research.

## Contribution

The study presents a 15-year global dataset combining genetic, clinical, cognitive, imaging, and biochemical data from individuals at risk for Alzheimer's.

## Key findings

- The dataset captures the progression from presymptomatic to symptomatic Alzheimer's in individuals with genetic mutations.
- It includes comprehensive data from both mutation carriers and non-carriers, enabling detailed comparisons.
- The study supports the development of preventive and therapeutic interventions for Alzheimer's disease.

## Abstract

The Dominantly Inherited Alzheimer Network Observational Study (DIAN Obs) is a longitudinal, global cohort study investigating brain aging and autosomal dominant Alzheimer’s disease (ADAD), a rare monogenic form of Alzheimer’s disease (AD). Established in 2008 with support from the National Institute on Aging (NIA), DIAN Obs is designed to collect comprehensive and uniform data with the aim to characterize brain biology and clinical trajectory of individuals at risk for ADAD. Mutations in the amyloid protein precursor (APP), presenilin 1 (PSEN1), or presenilin 2 (PSEN2) genes cause ADAD with virtually full penetrance and a predictable age at symptomatic onset. Participants, both mutation carriers and non-carriers from affected families, undergo longitudinal clinical and cognitive assessments, neurologic and physical examinations, structural and functional neuro-imaging, and amyloid and tau positron emission tomography (PET). Biospecimens include cerebrospinal fluid, plasma, serum, and whole blood for biochemical, genetic and multi-omic analyses, with brain donation upon death. This dataset enables one of the most detailed longitudinal examinations of the human brain across the continuum from presymptomatic to symptomatic AD. The extensive DIAN Obs data and biospecimen repository provides a globally accessible resource to advance understanding of AD pathophysiology, aging, and the development of preventive and therapeutic interventions.

## Linked entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351], PSEN1 (presenilin 1) [NCBI Gene 5663], PSEN2 (presenilin 2) [NCBI Gene 5664]
- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, PSEN1 (presenilin 1) [NCBI Gene 5663] {aka ACNINV3, AD3, CMD1U, FAD, PS-1, PS1}, NRGN (neurogranin) [NCBI Gene 4900] {aka RC3, hng}, PHF1 (PHD finger protein 1) [NCBI Gene 5252] {aka MTF2L2, PCL1, TDRD19C, hPHF1}, VSNL1 (visinin like 1) [NCBI Gene 7447] {aka HLP3, HPCAL3, HUVISL1, VILIP, VILIP-1}, CHI3L1 (chitinase 3 like 1) [NCBI Gene 1116] {aka ASRT7, CGP-39, GP-39, GP39, HC-gp39, HCGP-3P}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, GRN (granulin precursor) [NCBI Gene 2896] {aka CLN11, FTD2, GEP, GP88, PCDGF, PEPI}, PSEN2 (presenilin 2) [NCBI Gene 5664] {aka AD3L, AD4, CMD1V, PS2, STM2}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, SNAP25 (synaptosome associated protein 25) [NCBI Gene 6616] {aka CMS18, DEE117, RIC-4, RIC4, SEC9, SNAP}
- **Diseases:** neuronal injury (MESH:D009410), amyloidosis (MESH:D000686), Cortical hypometabolism (MESH:D054220), Dementia (MESH:D003704), Amyloid (MESH:C000718787), FTD (MESH:D057180), Cognitive decline (MESH:D003072), death (MESH:D003643), ATN (MESH:C536599), Stroke (MESH:D020521), Neurological Disorders (MESH:D009461), tangles (MESH:D055956), neuronal and synaptic injury (MESH:D012183), inflammation (MESH:D007249), neurodegeneration (MESH:D019636), Parkinson's disease (MESH:D010300), AD (MESH:D000544), neuroinflammation (MESH:D000090862), atrophy (MESH:D001284)
- **Chemicals:** AV1451 (MESH:C000591008), formalin (MESH:D005557), MK-6240 (MESH:C000618291), FTP (-), FDG (MESH:D019788), PI2620 (MESH:C000722249), PiB (MESH:C069442), paraffin (MESH:D010232)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909123/full.md

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Source: https://tomesphere.com/paper/PMC12909123