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Study of N-homocysteinylation of Key Proteins in Alzheimer's Disease (HO-MA)

Study of N-homocysteinylation of Key Proteins in Alzheimer's Disease

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06168955
Acronym
HO-MA
Enrollment
30
Registered
2023-12-13
Start date
2024-02-29
Completion date
2025-12-31
Last updated
2024-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease

Keywords

Alzheimer Disease, Genetic, N-homocysteinylation

Brief summary

Alzheimer's disease (AD) is the leading cause of dementia in France. It is a multifactorial pathology, combining genetic and environmental risk factors. Homocysteine, a sulfur-containing amino acid belonging to the methionine-monocarbon cycle, has frequently been found at high levels in neurodegenerative diseases, and in AD in particular. It has been shown on human brain sections that the interaction of homocysteine with tau and MAP1, two key AD proteins, was significantly higher in AD patients than in controls, and corresponded to an N-homocysteinylation type interaction. This is a prospective study, the main objective of which is to compare MAP1 N-homocysteinylation levels in fibroblasts from individuals with AD versus disease-free cell lines.

Interventions

OTHERskin biopsy

skin biopsy for cell culture and N-homocysteinylation study

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* age \> 18 years * Age of onset of AD \< 75 years * Person with AD with positive CSF biomarkers * Person who has previously benefited from an analysis of AD genetic characteristics (APP, PSEN1, PSEN2, TREM2, ABCA7, SORL1 genes and ApoE status) and an analysis of monocarbon metabolism genes in the case of biochemical abnormalities by clinical exome, targeted panel or complete exome, and for whom the data set is already available.

Exclusion criteria

* Pregnant, parturient or breast-feeding women * Minor (not emancipated) * Person of legal age (subject to a legal protection measure) * Adult unable to give consent

Design outcomes

Primary

MeasureTime frame
MAP1 homocysteinylation levelBaseline

Secondary

MeasureTime frame
Homocysteinylation level of tau proteinbaseline

Countries

France

Contacts

Primary ContactMathilde Renaud
cppest1@chlcdijon.fr0380425485

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026