2015
DOI: 10.1155/2015/571314
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Can Variability of Pattern ERG Signal Help to Detect Retinal Ganglion Cells Dysfunction in Glaucomatous Eyes?

Abstract: Objective. To evaluate variability of steady-state pattern electroretinogram (SS-PERG) signal in normal, suspected, and glaucomatous eyes. Methods. Twenty-one subjects with suspected glaucoma due to disc abnormalities (GS), 37 patients with early glaucoma (EG), and 24 normal control (NC) were tested with spectral-domain optical coherence tomography (SD-OCT), standard automated perimetry (SAP), and SS-PERG. Mean deviation (MD), pattern standard deviation (PSD), retinal nerve fiber layer (RNFL), and ganglionar c… Show more

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Cited by 21 publications
(29 citation statements)
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“…This difference in phase consistency is demonstrated in Figures c,d. A low ss‐PERG phase consistency and decreased amplitude have been previously seen in patients with glaucoma . Accordingly, we found MagnitudeD to be significantly lower in patients with glaucoma than in healthy controls.…”
Section: Discussionsupporting
confidence: 77%
“…This difference in phase consistency is demonstrated in Figures c,d. A low ss‐PERG phase consistency and decreased amplitude have been previously seen in patients with glaucoma . Accordingly, we found MagnitudeD to be significantly lower in patients with glaucoma than in healthy controls.…”
Section: Discussionsupporting
confidence: 77%
“…We considered a low amplitude in SS-PERG (<1.5 μm) and a high phase variability of PERG signal in RE-PERG (>0.15 SD) as pathologic. 36 , 41 …”
Section: Resultsmentioning
confidence: 99%
“…A similar electrode placed on the lid of the unstimulated eye was used as a reference, as described in other studies. 36 In all cases, the impedance was below 5 k. The responses were amplified (gain of 100,000), filtered (bandwidth: 130 Hz), and sampled with a resolution of 12 bits. The analysis time was equal to the time period of the stimulus (133 ms).…”
Section: Methodsmentioning
confidence: 99%
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“…Chromosome detection of amniotic fluid cells is an effective way to diagnose DS, but it has limitations, such as being a complicated process and it is time-consuming [ 12 , 13 ]. Noninvasive gene detection technique is a novel method for DS examination, and its theoretical basis is that blood of pregnant women contains genomic DNA of the fetus [ 14 16 ], which can help determine whether the fetus has trisomy 21 or ERG mutation by use of sequence comparative analysis based on DNA sequencing of the pregnant woman’s blood [ 17 ]. It is very difficult to detect a small amount of DNA from the fetus in the blood of a pregnant woman, which makes noninvasive gene detection difficult [ 18 ].…”
Section: Introductionmentioning
confidence: 99%