Evidence map›Paper›PMID 42183931›Full record

ArticleJapanese journal of radiology2026

Preoperative prediction of meningioma grade based on synthetic MRI quantitative T1 and T2 mapping.

Tsubasa Nakano, Junki Kamizono, Tomohito Hasegawa, Masanori Nakajo, Kiyohisa Kamimura, Ryota Nakanosono, Hiroaki Nagano, Koji Takumi, Ryoji Yamagishi, Fumitaka Ejima and 6 more

Abstract read
In one paragraph

Article in Japanese journal of radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Tsubasa NakanoDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan. tnakano0722@gmail.com.ORCID http://orcid.org/0009-0009-7071-9081
Junki KamizonoDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Tomohito HasegawaDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Masanori NakajoDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Kiyohisa KamimuraDepartment of Advanced Radiological Imaging, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Ryota NakanosonoDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Hiroaki NaganoDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Koji TakumiDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Ryoji YamagishiDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Fumitaka EjimaDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Fumiko KanzakiDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Nayuta HigaDepartment of Neurosurgery, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Hajime YonezawaDepartment of Neurosurgery, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Mari KirishimaDepartment of Pathology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Ikumi KitazonoDepartment of Pathology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Takashi YoshiuraDepartment of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to investigate the difference in T1, T2, and proton density (PD) values derived from synthetic magnetic resonance imaging (MRI) across various meningioma subtypes and their potential as imaging biomarkers for the World Health Organization (WHO) grade classification of meningioma. MATERIALS AND

methodsThis study retrospectively analyzed the data of 100 consecutive meningioma cases. Across subtypes and WHO grades, intratumoral T1, T2, PD, and apparent diffusion coefficient (ADC) values, along with tumor volume, were measured and compared, and the discriminative performance of each parameter was evaluated using the area under the receiver operating characteristic curve (AUC). Simple and multiple regression analyses were conducted to assess the associations between quantitative imaging parameters and atypical pathological features (4 ≥ mitotic findings/high power field; brain invasion; increased cellularity; small cells with high nuclear-to-cytoplasmic ratio; prominent nucleoli; sheeting; necrosis).

resultsAmong all subtypes, angiomatous, microcystic, and metaplastic meningioma demonstrated remarkable high T1 and T2 values. The AUCs for differentiating these subtypes from other subtypes were 0.97 for T1 value and 0.99 for T2 value. Volume (p < 0.001), T1 value (p < 0.001), T2 value (p = 0.002), and ADC value (p = 0.035) were significantly higher in high grade meningioma than low grade meningioma, with an AUC of 0.83 achieved by combining volume, T1, and ADC value. Multiple regression analysis revealed that volume was significantly associated with necrosis (p = 0.018), whereas T1 and T2 values were significantly associated with sheeting (p = 0.047 and 0.025 for T1 and T2).

conclusionT1 and T2 mappings may serve as useful quantitative imaging biomarkers for meningioma grading.

Indexed as

Magnetic Resonance ImagingMeningeal NeoplasmsMeningiomaAdultAgedFemaleHumansMaleMiddle AgedNeoplasm GradingPredictive Value of TestsRetrospective StudiesMeningiomaQuantificationSynthetic MRIT1 mapT2 mapTumor grading

Identifiers

PMID42183931
PMCPMC13526115

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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.