Evidence map›Paper›PMID 28420385›Full record

ReviewFluids and barriers of the CNS2017

Frontotemporal dementia as a comorbidity to idiopathic normal pressure hydrocephalus (iNPH): a short review of literature and an unusual case.

V E Korhonen, E Solje, N M Suhonen, T Rauramaa, R Vanninen, A M Remes, V Leinonen

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in Fluids and barriers of the CNS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 20% of its field
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

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.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Genetic Risk Factors in Normal Pressure Hydrocephalus: What We Know and What Is Next.Movement disorders : official journal of the Movement Disorder Society · 2025
    Pooled it
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  3. Review
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  11. Copy number loss inNeurology. Genetics · 2018
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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

7 authors at 4 institutions in 1 country.

V E KorhonenDepartment of Neurosurgery, Kuopio University Hospital, P.O. Box 100, 70029 KYS, Kuopio, Finland.
E SoljeInstitute of Clinical Medicine-Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
N M SuhonenMedical Research Center, Oulu University Hospital, P.O. Box 20, 90029, Oulu, Finland.
T RauramaaInstitute of Clinical Medicine-Pathology, School of Medicine, University of Eastern, Kuopio, Finland.
R VanninenDepartment of Radiology, Kuopio University Hospital, P.O. Box 100, 70029 KYS, Kuopio, Finland.
A M RemesInstitute of Clinical Medicine-Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
V LeinonenDepartment of Neurosurgery, Kuopio University Hospital, P.O. Box 100, 70029 KYS, Kuopio, Finland. ville.leinonen@kuh.fi.
University of Eastern Finland · FIKuopio University Hospital · FIOulu University Hospital · FIUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Behavioural variant frontotemporal dementia (bvFTD) and idiopathic normal pressure hydrocephalus (iNPH) are neurodegenerative diseases that can present with similar symptoms. These include decline in executive functions, psychomotor slowness, and behavioural and personality changes. Ventricular enlargement is a key radiological finding in iNPH that may also be present in bvFTD caused by the C9ORF72 expansion mutation. Due to this, bvFTD has been hypothesized as a potential comorbidity to iNPH but bvFTD patients have never been identified in studies focusing in clinical comorbidities with iNPH. Here we describe a patient with the C9ORF72 expansion-associated bvFTD who also showed enlarged ventricles on brain imaging. The main clinical symptoms were severe gait disturbances and psychiatric problems with mild cognitive decline. Cerebrospinal fluid removal increased the patient's walking speed, so a ventriculoperitoneal shunt was placed. After insertion of the shunt, there was a significant improvement in walking speed as well as mild improvement in cognitive function but not in neuropsychiatric symptoms relating to bvFTD. Comorbid iNPH should be considered in bvFTD patients who have enlarged ventricles and severely impaired gait.

Indexed as

BrainC9orf72 ProteinCerebrospinal Fluid ShuntsComorbidityFemaleFrontotemporal DementiaHumansHydrocephalus, Normal PressureMiddle AgedProteinsTrinucleotide Repeat ExpansionC9orf72 ProteinC9orf72 protein, humanProteinsC9ORF72 repeat expansionCSF shuntDementiaIdiopathic normal pressure hydrocephalusNeurodegeneration

Identifiers

PMID28420385
PMCPMC5395836
OpenAlexW2605986536

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.