Evidence map›Paper›PMID 40445293›Full record

ArticleCellular and molecular neurobiology2025

Fibrinogen and Complement Factor H Induce Parkinsonian and Cognitive Impairment-Like Features in Mice.

Aditi Naskar, Mahesha Sachin, Senjuti Sengupta, Pallavi Bhadrachalam, Shantala Hegde, Ravi Yadav, Pramod Kumar Pal, Phalguni Anand Alladi

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Article in Cellular and molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Aditi NaskarDepartment of Clinical Psychopharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences (NIMHANS), Hosur Road, Bengaluru, 560029, India.
Mahesha SachinDepartment of Clinical Psychopharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences (NIMHANS), Hosur Road, Bengaluru, 560029, India.
Senjuti SenguptaDepartment of Clinical Psychopharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences (NIMHANS), Hosur Road, Bengaluru, 560029, India.
Pallavi BhadrachalamDepartment of Clinical Psychopharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences (NIMHANS), Hosur Road, Bengaluru, 560029, India.
Shantala HegdeDepartment of Clinical Psychology, National Institute of Mental Health and Neurosciences, Hosur Road, Bengaluru, 560029, India.
Ravi YadavDepartment of Neurology, National Institute of Mental Health and Neurosciences, Hosur Road, Bengaluru, 560029, India.
Pramod Kumar PalDepartment of Neurology, National Institute of Mental Health and Neurosciences, Hosur Road, Bengaluru, 560029, India.
Phalguni Anand AlladiDepartment of Clinical Psychopharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences (NIMHANS), Hosur Road, Bengaluru, 560029, India. alladiphalguni@gmail.com.

Funding

ICMR BMS/TF/Trans-Neuro/2014-3424/Dec-15/48/ MH/Govt to PAAICMR SRFship to ANJNCASR- SUMMER RESEARCH FELLOWSHIP SRFP
6 · The paper itself

Abstract

Cognitive impairment is one of the non-motor symptoms of Parkinson's disease (PD), which may precede motor impairment. Biomarker(s) can help detect the cognitive dysfunction, much earlier in the disease and may differentiate PD patients with and without cognitive impairments. Animal model-based biomarker validation studies can provide better insights into pathogenesis and open up avenues for addressing therapeutics; however, such studies using non-genetic modalities, are few. Our earlier non-targeted label-free proteomics-assisted biomarker study on CSF of PD patients with cognitive impairment (PDCI), revealed the presence of elevated levels of fibrinogen and complement factor H (CFAH) in PDCI-CSF. We now intend to determine if these proteins harbor a pathogenic potential, when present above physiological levels. Native fibrinogen and recombinant CFAH were intraperitoneally injected in adult C57BL/6J mice and 48 h later the motor and cognitive behavior alongside neuroanatomical correlates were studied. The motor and cognitive deficits were complemented by degenerative changes in the SNpc, striatum, CA1 and subiculum in the injected mice. The altered gut microarchitecture suggests the possibility of other non-motor symptoms. Here, we show that fibrinogen and CFAH can potentially induce motor, and non-motor deficits in mice, akin to the PDCI-associated neuropathological deficits, and thus are potential biomarkers.

Indexed as

Cognitive DysfunctionComplement Factor HFibrinogenParkinson DiseaseAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLComplement Factor HFibrinogenAnimal modelCognitive impairmentComplement factor HCSF-biomarkerFibrinogenParkinson’s disease

Identifiers

PMID40445293
PMCPMC12125439

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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.