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Substantia Nigra MRI markers are lower in Alzheimer's disease and are linked to general cognitive function.

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Paper

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The authors' code

MATLAB · 24 lines · 1.1 KB · no license

  1. function calculate_diag_grp_diff_covars
  2. load CompleteData.mat
  3. covars={'dprime_new','NPT_global_score','age','sex','edyears','EstimatedTotalIntraCranialVol','WM','LAN','MEM','EXEC','VIS','totaltau','ratio_Abeta42_40_prec','phosphotau181'};
  4. statstbl=cell2table(cell(length(covars),1),"RowNames",covars,'VariableNames',{'result'});
  5. for a=1:length(covars)
  6. [~,b,c]=anova1(CompleteData.(covars{a}),CompleteData.diag,'off');
  7. F=round(b{contains(b(:,1),'Groups'),strcmp(b(1,:),'F')},2);
  8. p=round(b{contains(b(:,1),'Groups'),strcmp(b(1,:),'Prob>F')},2);
  9. diff=round(c.means(4)-c.means(1),2);
  10. statstbl{covars{a},1}={['F(3,156)=',num2str(F),', p=',num2str(p)]};
  11. end
  12. writetable(statstbl,'diagres_copy_paste.xlsx','WriteRowNames',true);
  13. for a=1:length(covars)
  14. [~,b,c]=anova1(CompleteData.(covars{a}),CompleteData.diag,'off');
  15. F=round(b{contains(b(:,1),'Groups'),strcmp(b(1,:),'F')},2);
  16. p=round(b{contains(b(:,1),'Groups'),strcmp(b(1,:),'Prob>F')},2);
  17. diff=round(c.means(4)-c.means(1),2);
  18. statstbl{covars{a},1}={['F(3,156)=',num2str(F),', p=',num2str(p),', AD-HC=',num2str(diff)]};
  19. end
  20. writetable(statstbl,'diagres.xlsx','WriteRowNames',true);
  21. end

calculate_diag_grp_diff_covars.m at commit 0c071eb, no license · at the source

Overview

Authors: Friedrich Krohn1, Mousumi Sarkar1, Hartmut Schütze1, Panagiotis Iliopoulos1, Lucía Penalba-Sánchez1,2, Dorothea Hämmerer1,2, Renat Yakupov1,2, Falk Lüsebrink1, Annika Spottke3, Anja Schneider3,4, Nina Roy3,4, Enise Incesoy1,2,5, Michael Heneka3,6, Ingo Kilimann7, Luca Kleineidam3,4, Stefan J Teipel7, Frederic Brosseron3, Doreen Goerss3,4, Wenzel Glanz1,2, Matthias Schmid8
and 6 other authorsAyda Rostamzadeh9, Michael Wagner3,4, Klaus Fliessbach3,4, Frank Olaf Jessen10, Emrah Düzel1,2, Matthew J Betts1,2
  1. Institute of Cognitive Neurology and Dementia Research (IKND), Otto-von-Guericke University, Magdeburg 39120, Germany
  2. Betts Group, German Center for Neurodegenerative Diseases, Magdeburg 39120, Germany
  3. Leitung klinische Forschung, German Center for Neurodegenerative Diseases, Bonn 53127, Germany
  4. Department of Old Age Psychiatry and Cognitive Disorders, 53127 University Hospital Bonn, Bonn, Germany
  5. Department for Psychiatry and Psychotherapy, University Clinic Magdeburg, 39120 Magdeburg, Germany
  6. Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Belvaux 4367, Luxembourg
  7. Klinische Demenzforschung, German Center for Neurodegenerative Diseases, Rostock 18147, Germany
  8. Institute for Medical Biometry, Informatics and Epidemiology, Medical Faculty, University of Bonn, Bonn 53127, Germany
  9. Department of Psychiatry, Medical Faculty, University of Cologne, Cologne 50924, Germany
  10. Faculty of Medicine, University of Cologne, Cologne 50932, Germany
Journal: Brain communications, volume 8, issue 4, article fcag238
Dates: received 22 October 2024; accepted 4 April 2026; published online 24 June 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1093/braincomms/fcag238 · PMID 42488758 · PMCID PMC13390642 · OpenAlex W7165726884
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: structural MRI / diffusion (modality), human (organism), Alzheimer's / dementia (population), cognitive (subfield)
Methods: Connectivity, Statistics, fMRI & imaging
Keywords: Substantia Nigra (SN), Alzheimer's disease, neuromelanin, memory, novelty
Topic: Dementia and Cognitive Impairment Research (Psychiatry and Mental health, Medicine), according to OpenAlex
Citations: not cited yet (Europe PMC); 98 references in the paper

Abstract

Individuals with Alzheimer’s disease dementia show Alzheimer's disease pathology and a heterogeneous degeneration of the Substantia Nigra (SN) post-mortem. However, it is unclear how SN degeneration is related to cognitive dysfunction across the Alzheimer’s disease dementia continuum. In this study, using data from the prospective DZNE-Longitudinal Cognitive Impairment and Dementia Study (DELCODE), we investigated whether in vivo SN MRI measures are lower in individuals with clinically defined Alzheimer’s disease dementia than in healthy control subjects (HC) and if they are associated with hippocampal functional activity during the processing of novel visual stimuli and subsequent recognition memory. One hundred and sixty DELCODE participants (69 years ± 6 years, 88 men), including 79 HC, 70 individuals with subjective cognitive decline (SCD), 17 individuals with mild cognitive impairment (MCI) and 10 individuals with Alzheimer’s disease dementia, completed a scene novelty and encoding task and a 3T SN-sensitive MRI scan, from which the two in vivo SN measures MRI contrast and volume were calculated and harmonized between scanner sites while preserving diagnostic group differences. For 71 individuals, CSF levels of phosphoTau, total tau and amyloid-beta 42/40 ratio (Aß42/40) were available. All individuals completed a neuropsychological task battery from which a global cognitive score was calculated. In separate models, we assessed the relationship between SN MRI markers and CSF levels of Alzheimer’s disease, the global cognitive score, hippocampal novelty activation and recognition memory while accounting for age, sex, years of education and total intracranial volume (TIV). SN volume but not SN MRI contrast was lower in individuals with clinical Alzheimer’s disease dementia [one-way analyses of covariance (ANCOVA); F(156,4) = 5.6665, P = 0.0010, n = 160]. SN MRI contrast and volume were not associated with Aß42/40, ptau and total tau CSF levels (all P > 0.1) or hippocampal novelty activation (all P > 0.1). Moreover, SN volume was positively associated with recognition memory (R2 = 0.07, P < 0.001, n = 159), global cognition (R2= 0.38, P < 0.0001, n = 160) and years of education (R2 = 0.03, P = 0.036, n = 160). Our study emphasizes the potential of using in vivo SN MRI markers to study the impact of SN degeneration on general cognitive impairment and recognition memory in an Alzheimer’s disease dementia cohort. Our results motivate future longitudinal studies to explore how SN volume and SN contrast change with disease progression, how these are differentially associated with cognitive decline, and how SN volume and SN contrast might be related to other dopamine-dependent cognitive functions and dysfunctions.

Reproduced under the paper's license (CC BY), from the paper cited above.

Repository

Its files are read in the Code ↔ Paper reader above.

frikro/SN-Novelty-Brain-Comm

License: none: the authors keep all their rights
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 0c071ebcf485fbca719ce384e8ddbe1c75aec56d, 9 December 2025
Languages: MATLAB (6), Python (1)
Size: 8 files, 7 scripts
Software Heritage: not archived
Found in: “Data availability”
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Tools: Statistics and Machine Learning Toolbox (3 files), SPM (2 files), pandas (1 file), Pingouin (1 file), statsmodels (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
7 files

The paper's code and data availability statement is in the Data section.

Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 7 scripts, each with its path and the digest of its content;
  • no match between paragraphs and code yet;
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

No dataset and no data link were found in the paper.

Data availability

Data, study protocol and biomaterials can be shared with partners based on individual data and biomaterial transfer agreements. Scripts used for data analyses of this manuscript can be found here: https://github.com/frikro/SN-Novelty-Brain-Comm.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 2, 28 September 2026

  • Funding: added Deutsche Forschungsgemeinschaft: 425899996; Deutsches Zentrum für Neurodegenerative Erkrankungen: BN012; Otto von Guericke University Magdeburg

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 26 authors, 5 keywords, 88 references.

Cite

This paper

Krohn, F., Sarkar, M., Schütze, H., Iliopoulos, P., Penalba-Sánchez, L., Hämmerer, D., Yakupov, R., Lüsebrink, F., Spottke, A., Schneider, A., Roy, N., Incesoy, E., Heneka, M., Kilimann, I., Kleineidam, L., Teipel, S. J., Brosseron, F., Goerss, D., Glanz, W., . . . Betts, M. J. (2026). Substantia Nigra MRI markers are lower in Alzheimer's disease and are linked to general cognitive function. Brain communications, 8(4), fcag238. https://doi.org/10.1093/braincomms/fcag238

BibTeX

@article{krohn2026substantia,
author = {Krohn, Friedrich and Sarkar, Mousumi and Schütze, Hartmut and Iliopoulos, Panagiotis and Penalba-Sánchez, Lucía and Hämmerer, Dorothea and Yakupov, Renat and Lüsebrink, Falk and Spottke, Annika and Schneider, Anja and Roy, Nina and Incesoy, Enise and Heneka, Michael and Kilimann, Ingo and Kleineidam, Luca and Teipel, Stefan J and Brosseron, Frederic and Goerss, Doreen and Glanz, Wenzel and Schmid, Matthias and Rostamzadeh, Ayda and Wagner, Michael and Fliessbach, Klaus and Jessen, Frank Olaf and Düzel, Emrah and Betts, Matthew J},
title = {{Substantia Nigra MRI markers are lower in Alzheimer's disease and are linked to general cognitive function}},
journal = {Brain communications},
year = {2026},
month = jun,
volume = {8},
number = {4},
pages = {fcag238},
publisher = {Oxford University Press},
issn = {2632-1297},
doi = {10.1093/braincomms/fcag238},
url = {https://doi.org/10.1093/braincomms/fcag238},
pmid = {42488758},
pmcid = {PMC13390642}
}

RIS

TY - JOUR
AU - Krohn, Friedrich
AU - Sarkar, Mousumi
AU - Schütze, Hartmut
AU - Iliopoulos, Panagiotis
AU - Penalba-Sánchez, Lucía
AU - Hämmerer, Dorothea
AU - Yakupov, Renat
AU - Lüsebrink, Falk
AU - Spottke, Annika
AU - Schneider, Anja
AU - Roy, Nina
AU - Incesoy, Enise
AU - Heneka, Michael
AU - Kilimann, Ingo
AU - Kleineidam, Luca
AU - Teipel, Stefan J
AU - Brosseron, Frederic
AU - Goerss, Doreen
AU - Glanz, Wenzel
AU - Schmid, Matthias
AU - Rostamzadeh, Ayda
AU - Wagner, Michael
AU - Fliessbach, Klaus
AU - Jessen, Frank Olaf
AU - Düzel, Emrah
AU - Betts, Matthew J
TI - Substantia Nigra MRI markers are lower in Alzheimer's disease and are linked to general cognitive function
T2 - Brain communications
J2 - Brain Commun
PY - 2026
DA - 2026/06/24
VL - 8
IS - 4
SP - fcag238
SN - 2632-1297
PB - Oxford University Press
DO - 10.1093/braincomms/fcag238
UR - https://doi.org/10.1093/braincomms/fcag238
LA - en
ER -

CSL-JSON

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