Evidence map›Paper›PMID 24715861›Full record

ArticleFrontiers in aging neuroscience2014

MTA index: a simple 2D-method for assessing atrophy of the medial temporal lobe using clinically available neuroimaging.

Manuel Menéndez-González, Alfonso López-Muñiz, José A Vega, José M Salas-Pacheco, Oscar Arias-Carrión

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2014. 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
–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

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.

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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

5 authors.

Manuel Menéndez-GonzálezUnidad de Neurología, Hospital Álvarez-Buylla Mieres, Spain ; Departamento de Morfología y Biología Celular, Universidad de Oviedo Oviedo, Spain ; Instituto de Neurociencias, Universidad de Oviedo Oviedo, Spain.
Alfonso López-MuñizDepartamento de Morfología y Biología Celular, Universidad de Oviedo Oviedo, Spain ; Instituto de Neurociencias, Universidad de Oviedo Oviedo, Spain.
José A VegaDepartamento de Morfología y Biología Celular, Universidad de Oviedo Oviedo, Spain.
José M Salas-PachecoInstituto de Investigación Científica, Universidad Juárez del Estado de Durango Durango, México.
Oscar Arias-CarriónUnidad de Trastornos del Movimiento y Sueño (TMS), Hospital General Dr. Manuel Gea González/UNAM México DF, Mexico ; Unidad de Trastornos del Movimiento y Sueño (TMS), Hospital General Ajusco Medio México DF, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeDespite a strong correlation to severity of AD pathology, the measurement of medial temporal lobe atrophy (MTA) is not being widely used in daily clinical practice as a criterion in the diagnosis of prodromal and probable AD. This is mainly because the methods available to date are sophisticated and difficult to implement for routine use in most hospitals-volumetric methods-or lack objectivity-visual rating scales. In this pilot study we aim to describe a new, simple and objective method for measuring the rate of MTA in relation to the global atrophy using clinically available neuroimaging and describe the rationale behind this method. DESCRIPTION: This method consists of calculating a ratio with the area of 3 regions traced manually on one single coronal MRI slide at the level of the interpeduncular fossa: (1) the medial temporal lobe (MTL) region (A); (2) the parenchima within the medial temporal region, that includes the hippocampus and the parahippocampal gyrus-the fimbria taenia and plexus choroideus are excluded-(B); and (3) the body of the ipsilateral lateral ventricle (C). Therefrom we can compute the ratio "Medial Temporal Atrophy index" at both sides as follows: MTAi = (A - B)× 10/C.

conclusionsThe MTAi is a simple 2D-method for measuring the relative extent of atrophy in the MTL in relation to the global brain atrophy. This method can be useful for a more accurate diagnosis of AD in routine clinical practice. Further studies are needed to assess the usefulness of MTAi in the diagnosis of early AD, in tracking the progression of AD and in the differential diagnosis of AD with other dementias.

Indexed as

Alzheimerbiomarkerdiagnosismedial temporal lobe atrophymild cognitive impairmentMRIneuroimaging

Identifiers

PMID24715861
PMCPMC3970022

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