Evidence map›Paper›PMID 22581443›Full record

ArticleMagma (New York, N.Y.)2012

Evaluation of a mobile NMR sensor for determining skin layers and locally estimating the T(2eff) relaxation time in the lower arm.

Darius Kornetka, Martin Trammer, Jochen Zange

Abstract read
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In one paragraph

Article in Magma (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

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

3 authors at 1 institution in 1 country.

Darius KornetkaInstitute of Aerospace Medicine, Deutsches Zentrum für Luft- und Raumfahrt, DLR eV, Linder Höhe, 51147 Cologne, Germany. darius.kornetka@dlr.de
Martin Trammer
Jochen Zange
Deutsches Zentrum für Luft- und Raumfahrt e. V. (DLR) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectThe nuclear magnetic resonance (NMR) mobile-universal-surface-explorer (MOUSE) was evaluated in a pilot study to determine its ability to detect physiological changes in human skin caused by physical or pharmacological interventions. MATERIALS AND

methodsThe left lower arm skin thicknesses of ten male subjects were measured five times using a Profile NMR-MOUSE(®) ((1)H, 19 MHz) before and after a venous occlusion manoeuvre. In five of the subjects, the T(2eff) relaxation times were derived from a bi-exponential fitting and were determined in the dermis and subcutis before and after applying a salve containing capsaicin.

resultsThe dermis (including the epidermis) showed rather homogeneous signal amplitudes. The subcutis was characterised by higher and more variable amplitudes. The full-skin thickness values were affirmed by ultrasound imaging. The NMR profiles did not show significant skin swelling due to venous occlusion. In the dermis, capsaicin caused significant (p < 0.05) decreases in both components of T(2eff) (100 ± 19 ms-19 ± 10 ms; 9.5 ± 0.5 ms-7.2 ± 1.6 ms). In the subcutis, the T(2eff) was not affected.

conclusionIn principle, NMR-MOUSE profiles are capable of detecting skin structure. However, precise measurements are jeopardised by poor reproducibility, long acquisition times, and incompatibility between the geometries of the sensitive area of the instrument and the non-planar structure of the skin. In the dermis, T(2eff) contrast could be used to detect the changes in tissue composition caused by inflammatory reactions.

Indexed as

AdultAlgorithmsBody Mass IndexDermisEpidermisEquipment DesignHumansMagnetic Resonance SpectroscopyMagneticsMaleModels, StatisticalPilot ProjectsReproducibility of ResultsSkinSurface PropertiesUltrasonography

Identifiers

PMID22581443
OpenAlexW2005876142

What OpenQuestion holds

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Registered trials

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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.