ADC values of benign and high grade meningiomas and associations with tumor cellularity and proliferation - A systematic review and meta-analysis.

Abstract:

INTRODUCTION:The aim of the present systematic review and meta-analysis was to compare the reported ADC values in different meningiomas and to analyze associations between ADC and cell count and proliferation activity in this tumor entity. METHOD:MEDLINE library and SCOPUS database were screened for papers investigating ADC values of meningiomas up November 2019. The first primary endpoint of the systematic review was the reported ADC mean value of the meningioma groups. The second primary endpoint was the correlation coefficient between ADC values and proliferation index Ki 67 and cellularity. RESULTS:For the discrimination analysis between benign and high grade meningioma 17 studies were suitable. There were 766 grade I tumors and 289 high grade meningiomas. The calculated mean ADC value of the benign grade I tumors was 0.93 × 10-3mm2/s [95%-Confidence interval 0.84;1.03] and the mean value of the high-grade tumors was 0.77 × 10-3mm2/s [95%-Confidence interval 0.73-0.80]. The pooled correlation coefficient between ADC and the proliferation index Ki 67 was r = -0.36 [95% CI -0.43; -0.28]. The pooled correlation coefficient between ADC and cellularity was r = -0.43 [95% CI -0.61; - 0.26]. CONCLUSION:No validated ADC threshold can be recommended for distinguishing benign from high grade meningiomas. Only a moderate inverse correlation was identified between ADC values and tumor microstructure in meningiomas and, therefore, ADC might not accurately enough to predict proliferation potential and cellularity in this entity.

journal_name

J Neurol Sci

authors

Meyer HJ,Wienke A,Surov A

doi

10.1016/j.jns.2020.116975

subject

Has Abstract

pub_date

2020-08-15 00:00:00

pages

116975

eissn

0022-510X

issn

1878-5883

pii

S0022-510X(20)30312-9

journal_volume

415

pub_type

杂志文章
  • Magnetization transfer histogram parameters reflect all dimensions of MS pathology, including atrophy.

    abstract:INTRODUCTION:Magnetization transfer ratio (MTR) histogram analysis can be used as a method for quantifying overall disease burden in MS. We studied correlations between MTR histogram and clinical parameters in MS subgroups. Contrary to earlier studies we placed special emphasis on the lower MTR range, to explore the ef...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(01)00431-2

    authors: Kalkers NF,Hintzen RQ,van Waesberghe JH,Lazeron RH,van Schijndel RA,Adèr HJ,Polman CH,Barkhof F

    更新日期:2001-03-01 00:00:00

  • Neuroprotective effect of diazoxide on brain injury induced by cerebral ischemia/reperfusion during deep hypothermia.

    abstract:OBJECT:The purpose of this study was to determine the effects of diazoxide on apoptosis and the relative mechanisms in a model of brain injury induced by cerebral ischemia/reperfusion (I/R) during deep hypothermia. METHODS:Three-week-old Sprague-Dawley male rats were randomly and equitably divided into sham-operated g...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2007.10.029

    authors: He X,Mo X,Gu H,Chen F,Gu Q,Peng W,Qi J,Shen L,Sun J,Zhang R,Kj Y

    更新日期:2008-05-15 00:00:00

  • Motor neuron disease in the province of Turin, Italy, 1966-1980. Survival analysis in an unselected population.

    abstract::We performed a population based survival analysis of all incident cases (220) of motor neuron disease (MND) in the province of Turin, Italy, during the period 1966-1980. 175 cases were diagnosed as amyotrophic lateral sclerosis (ALS), 43 as progressive muscular atrophy (PMA) and 2 as progressive bulbar palsy (PBP). Th...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(84)90004-2

    authors: Mortara P,Chiò A,Rosso MG,Leone M,Schiffer D

    更新日期:1984-11-01 00:00:00

  • Neurogenomics in Africa: Perspectives, progress, possibilities and priorities.

    abstract::The understanding of the genetic basis of neurological disorders has grown rapidly in the last two decades. Despite the genomic heterogeneity within African populations, large-scale candidate gene or linkage and exome studies are lacking. However, current knowledge on neurogenetics in African populations is limited an...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2016.05.006

    authors: Akinyemi RO,Owolabi MO,Oyeniyi T,Ovbiagele B,Arnett DK,Tiwari HK,Walker R,Ogunniyi A,Kalaria RN,SIREN group of H3Africa Consortium.

    更新日期:2016-07-15 00:00:00

  • Serum anti-brain endothelium antibodies and cognitive assessment in patients with Binswanger's encephalopathy.

    abstract::The pathogenic mechanism underlying the vascular changes in Binswanger's encephalopathy (BE) is unknown. To test whether alterations of the humoral immunity may lead to endothelium damage, we analyzed serum levels of anti-brain endothelium antibodies (ABEA) (IgG and IgM) in 16 BE patients, 19 subjects with ischemic va...

    journal_title:Journal of the neurological sciences

    pub_type: 临床试验,杂志文章

    doi:10.1016/0022-510x(94)00215-a

    authors: Annunziata P,Cioni C,Moschini F,Riccucci A,Guazzi GC

    更新日期:1995-01-01 00:00:00

  • Fingerprint inclusions. Ultrastructural demonstration of muscle fiber type specificity.

    abstract::Fingerprint inclusions were identified in the skeletal muscle of a child with severe hypotonia. The mean Z-line and M-line widths from each of 19 muscle fibers containing the fingerprint inclusions were calculated. The mean Z-line widths were 85-99 nm, and the mean M-line widths were 75-101 nm. According to out presen...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(77)90216-7

    authors: Payne CM,Curless RG

    更新日期:1977-04-01 00:00:00

  • Affinity immunoblotting: rapid and sensitive detection of oligoclonal IgG, IgA and IgM in unconcentrated CSF by agarose isoelectric focusing.

    abstract::Two methods for the investigation of oligoclonal immunoglobulin bands in cerebrospinal fluid are compared. Isoelectric focusing (IEF) in agarose gels combined with a highly sensitive affinity immunoblotting proved to be superior to PAGE-IEF and silver staining regarding detection sensitivity and expenditure of labour....

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(91)90167-6

    authors: Kaiser R

    更新日期:1991-06-01 00:00:00

  • The molecular genetics of familial Creutzfeldt-Jakob disease in France.

    abstract::Five French families with Creutzfeldt-Jakob disease (CJD) were found to have either of 2 different point mutations (at codons 178 and 200) in the amyloid precursor gene (PRNP) on chromosome 20. The ancestry of these and other CJD families outside of France suggests that the codon 178 mutation had a northern European o...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(91)90151-v

    authors: Brown P,Goldfarb LG,Cathala F,Vrbovská A,Sulima M,Nieto A,Gibbs CJ Jr,Gajdusek DC

    更新日期:1991-10-01 00:00:00

  • Sensorimotor network in cervical dystonia and the effect of botulinum toxin treatment: a functional MRI study.

    abstract:BACKGROUND:The evidence suggests that the origin of primary dystonia is at least partly associated with widespread dysfunction of the basal ganglia and cortico-striato-thalamo-cortical circuits. The aim of the study was to assess the sensorimotor activation pattern outside the circuits controlling the affected body par...

    journal_title:Journal of the neurological sciences

    pub_type: 临床试验,杂志文章

    doi:10.1016/j.jns.2011.03.040

    authors: Opavský R,Hluštík P,Otruba P,Kaňovský P

    更新日期:2011-07-15 00:00:00

  • The MPTP model: versatile contributions to the treatment of idiopathic Parkinson's disease.

    abstract::In human and subhuman primates, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) produces irreversible clinical, biochemical and neuropathological alterations highly reminiscent of those observed in Parkinson's disease. The MPTP model has provided the best available tool to date for the assessment of efficacy and s...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/0022-510x(90)90225-c

    authors: Bloem BR,Irwin I,Buruma OJ,Haan J,Roos RA,Tetrud JW,Langston JW

    更新日期:1990-07-01 00:00:00

  • New options for early treatment of multiple sclerosis.

    abstract::It is now possible to diagnose patients with multiple sclerosis earlier than previously due to the integration of MRI parameters into the diagnostic criteria. This provides a window of opportunity to treat patients with disease-modifying treatments before clinically-manifest tissue destruction and disability has emerg...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/S0022-510X(09)70004-8

    authors: Tintoré M

    更新日期:2009-02-01 00:00:00

  • Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero (MPZ/P0).

    abstract::Hereditary motor and sensory neuropathy (HMSN), also known as Charcot-Marie-Tooth disease (CMT) is a group of clinically and genetically heterogeneous neuropathies classically divided into demyelinating (CMT1) and axonal forms (CMT2). The most common demyelinating form is CMT1A with an underlying duplication in the ge...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2009.03.008

    authors: Zschüntzsch J,Dibaj P,Pilgram S,Kötting J,Gerding WM,Neusch C

    更新日期:2009-06-15 00:00:00

  • A minute demyelinating lesion causing acute positional vertigo.

    abstract::Clinico-anatomical correlations in multiple sclerosis patients presenting with central positional vertigo are lacking. We report on a patient with acute onset positional vertigo mimicking benign paroxysmal positional vertigo with a single enhancing lesion in the inner part of the superior cerebellar peduncle, disclose...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2007.09.013

    authors: Anagnostou E,Varaki K,Anastasopoulos D

    更新日期:2008-03-15 00:00:00

  • Changes in tetrodotoxin-resistant action potentials after passive transfer of myasthenia gravis patient sera.

    abstract::Muscle electrical activity has been studied in mice after intraperitoneal injection of sera from myasthenia gravis (MG) patients. Myasthenic serum did not modify the electrical properties of innervated muscle fibres. The resting membrane potential and the action potential parameters remained unchanged. However, tetrod...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(89)90063-4

    authors: Losavio A,Muchnik S,Sica RE,Panizza M

    更新日期:1989-07-01 00:00:00

  • Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?

    abstract::Human carnitine palmitoyltransferase (CPT) deficiency results in 2 clinical forms: a more common "muscular form" with myoglobinuria with or without delayed or impaired ketogenesis and a rare "hepatic form" with hypoketotic hypoglycemia, encephalopathy and seizures without muscular manifestations. We present 2 patients...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(89)90139-1

    authors: Tein I,Demaugre F,Bonnefont JP,Saudubray JM

    更新日期:1989-09-01 00:00:00

  • Exploring outcomes and characteristics of myasthenia gravis: Rationale, aims and design of registry - The EXPLORE-MG registry.

    abstract:OBJECTIVES:Though much information exists about the diagnosis, treatment, and epidemiology of myasthenia gravis (MG), a comprehensive data registry and biorepository is critical to better understand disease mechanisms, treatment outcomes, and the impact of treatment strategies. We aimed to design and implement the "Exp...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2020.116830

    authors: Anil R,Kumar A,Alaparthi S,Sharma A,Nye JL,Roy B,O'Connor KC,Nowak RJ

    更新日期:2020-07-15 00:00:00

  • Acute loss of spatial navigational skills in a case of a right posterior hippocampus stroke.

    abstract::The ability to accurately navigate within an environment (known or new) is not fully understood but involves a number of highly complicated cognitive process related to both central and peripheral nervous system structures and neuronal networks. We describe a patient who developed loss of his spatial navigational skil...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2011.06.026

    authors: Aradillas E,Libon DJ,Schwartzman RJ

    更新日期:2011-09-15 00:00:00

  • Infarct presenting with a combination of Wallenberg and posterior spinal artery syndromes.

    abstract::This is the first report of a patient presenting with a combination of Wallenberg and posterior spinal artery syndromes. The patient developed right hemiplegia and sensory disturbances on the right side of the face and over the whole body. MRI showed infarcts of the cerebellum, medulla oblongata, and upper cervical co...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(00)00318-x

    authors: Manabe Y,Murase T,Iwatsuki K,Warita H,Hayashi T,Sakai K,Abe K

    更新日期:2000-06-15 00:00:00

  • Granulocyte dysfunction and myotonic dystrophy.

    abstract::A 52-year-old Caucasian male with typical features of myotonic dystrophy (MD) developed a lung abscess and was found to have a mild atypical cyclic neutropenia. Granulocyte function testing revealed a defect in phagocytosis, bactericidal activity and chemotaxis. The defects were less severe at the nadir of the granulo...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(86)90057-2

    authors: Friedenberg WR,Marx JJ Jr,Hansotia P,Gottschalk PG

    更新日期:1986-03-01 00:00:00

  • Cognitive impairment and hypothymia in post stroke patients.

    abstract::129 patients aged 18-84 in early rehabilitation period of the first hemispheric ischemic stroke and 48 patients with cerebrovascular disorders without stroke in anamnesis were observed. Cognitive functions (MMSE, FAB, Clock Drawing Test, the 5-Word test, attention assessment, Semantic Verbal Fluency test) and emotiona...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2012.11.013

    authors: Pustokhanova L,Morozova E

    更新日期:2013-02-15 00:00:00

  • Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations.

    abstract:BACKGROUND:Glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase (GNE) myopathy, also called distal myopathy with rimmed vacuoles (DMRV) or hereditary inclusion body myopathy (HIBM), is a rare, progressive autosomal recessive disorder caused by mutations in the GNE gene. Here, we examined the relationship b...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2012.03.016

    authors: Mori-Yoshimura M,Monma K,Suzuki N,Aoki M,Kumamoto T,Tanaka K,Tomimitsu H,Nakano S,Sonoo M,Shimizu J,Sugie K,Nakamura H,Oya Y,Hayashi YK,Malicdan MC,Noguchi S,Murata M,Nishino I

    更新日期:2012-07-15 00:00:00

  • Altered tumor growth factor beta mRNA expression is associated with thymectomy-related clinical remission in myasthenia gravis.

    abstract::Clinical remission in myasthenia gravis after thymectomy and immune suppressive treatment may be reflected by changes of immunoregulatory cytokines. Mononuclear cells from paired blood samples from fifteen patients with myasthenia gravis before and after thymectomy and immunosuppressive therapy were examined by in sit...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(97)00104-4

    authors: Weissert R,Melms A,Link H

    更新日期:1997-10-03 00:00:00

  • Neuromyelitis optica spectrum disorders with antibodies to myelin oligodendrocyte glycoprotein or aquaporin-4: Clinical and paraclinical characteristics in Algerian patients.

    abstract:BACKGROUND:Neuromyelitis optica (NMO) is a severe autoimmune inflammatory disorder of the central nervous system. NMO and its abortive forms are referred to as NMO spectrum disorders (NMOSD). NMOSD are mostly associated with antibodies to aquaporin-4 (AQP4-IgG). However, recent studies have demonstrated antibodies to m...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2017.08.3254

    authors: Bouzar M,Daoudi S,Hattab S,Bouzar AA,Deiva K,Wildemann B,Reindl M,Jarius S

    更新日期:2017-10-15 00:00:00

  • Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase.

    abstract::We examined the characteristic clinical features of one family of familial amyotrophic lateral sclerosis (FALS) with a His46Arg mutation in the enzyme Cu/Zn superoxide dismutase-1 (SOD1). The disease duration for this family was 18.1 +/- 13.2 (mean +/- S.D.) years, with the age at onset being 39.7 +/- 10.5 years old (...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/s0022-510x(02)00054-0

    authors: Ohi T,Saita K,Takechi S,Nabesima K,Tashiro H,Shiomi K,Sugimoto S,Akematsu T,Nakayama T,Iwaki T,Matsukura S

    更新日期:2002-05-15 00:00:00

  • Stroke admission and case-fatality in an urban medical unit in sub-Saharan Africa: a fourteen year trend study from 1999 to 2012.

    abstract:BACKGROUND:Data on recent stroke trends in the context of rapidly deteriorating risk profile of populations within Africa is very limited. We investigated the admission trend for stroke and related outcomes in a major referral hospital in Cameroon. METHODS:Admission and discharge registries, and patient files for the ...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/j.jns.2015.02.002

    authors: Lekoubou A,Nkoke C,Dzudie A,Kengne AP

    更新日期:2015-03-15 00:00:00

  • Concomitant administration of sodium dichloroacetate and thiamine in west syndrome caused by thiamine-responsive pyruvate dehydrogenase complex deficiency.

    abstract::We treated a female patient with West syndrome caused by thiamine-responsive pyruvate dehydrogenase complex (PDHC) deficiency. Infantile spasms occurred in association with elevated blood and CSF lactate concentrations; these symptoms disappeared when lactate concentrations had been lowered by treatment with concomita...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/s0022-510x(99)00250-6

    authors: Naito E,Ito M,Yokota I,Saijo T,Chen S,Maehara M,Kuroda Y

    更新日期:1999-12-01 00:00:00

  • Effect of thyroxine on the development of somatosensory and visual evoked potentials in the rat.

    abstract::The thyroid hormone thyroxine (T4), administered post-natally to neonatal rats, has been shown to accelerate development of auditory function, as expressed by auditory nerve-brainstem evoked responses. This study investigated whether this earlier development was also reflected in other sensory modalities. Rat pups wer...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(94)00229-h

    authors: Freeman S,Sohmer H

    更新日期:1995-02-01 00:00:00

  • Abnormalities of visual function in hereditary motor and sensory neuropathy.

    abstract::Visual function was studied in a group of 15 patients with hereditary motor and sensory neuropathy (HMSN). Psychophysical measures of luminance and chromatic threshold and temporal contrast sensitivity were undertaken, together with visual evoked potentials (VEPs), visual fields and clinical neuro-ophthalmological exa...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章

    doi:10.1016/0022-510x(93)90296-b

    authors: Honan WP,Heron JR,Foster DH,Edgar GK,Scase MO

    更新日期:1993-02-01 00:00:00

  • Hemispheric differences in malignant middle cerebral artery stroke.

    abstract:BACKGROUND:We recently reported that left versus right hemisphere cerebral infarctions patients more frequently have worse outcomes. However our clinical experience led us to suspect that the incidence of malignant middle cerebral artery infarctions (MMCA) was higher in the right compared to the left hemispheric stroke...

    journal_title:Journal of the neurological sciences

    pub_type: 杂志文章,评审

    doi:10.1016/j.jns.2015.04.036

    authors: Rastogi V,Lamb DG,Williamson JB,Stead TS,Penumudi R,Bidari S,Ganti L,Heilman KM,Hedna VS

    更新日期:2015-01-01 00:00:00

  • A longitudinal brain MRI study comparing the sensitivities of the conventional and a newer approach for detecting active lesions in multiple sclerosis.

    abstract::Monthly dual-echo spin-echo (SE) and enhanced magnetic resonance imaging (MRI) after the injection of a standard dose (SD) of gadolinium (Gd) is the conventional approach to monitor short-term disease activity in multiple sclerosis (MS). In this study, the sensitivity of this approach in detecting active lesions in MS...

    journal_title:Journal of the neurological sciences

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/s0022-510x(98)00144-0

    authors: Filippi M,Mastronardo G,Bastianello S,Rocca MA,Rovaris M,Gasperini C,Pozzilli C,Comi G

    更新日期:1998-07-15 00:00:00