Evidence map›Paper›PMID 34932062›Full record

ArticleInvestigative ophthalmology & visual science2021

Analysis of Microvasculature in Nonhuman Primate Macula With Acute Elevated Intraocular Pressure Using Optical Coherence Tomography Angiography.

Mihyun Choi, Seong-Woo Kim, Thi Que Anh Vu, Young-Jin Kim, Hachul Jung, Donggwan Shin, Heejong Eom, Young Ho Kim, Cheolmin Yun, Yong Yeon Kim

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Mihyun ChoiDepartment of Ophthalmology, Korea University Medicine, Seoul, Republic of Korea.
Seong-Woo KimDepartment of Ophthalmology, Korea University Medicine, Seoul, Republic of Korea.
Thi Que Anh VuDepartment of Ophthalmology, Hanoi Medical University, Hanoi, Vietnam.
Young-Jin KimMedical Device Development Center, Osong Medical Innovation Foundation, Cheongju, Chungbuk, Republic of Korea.
Hachul JungMedical Device Development Center, Osong Medical Innovation Foundation, Cheongju, Chungbuk, Republic of Korea.
Donggwan ShinLaboratory Animal Center, Osong Medical Innovation Foundation, Cheongju, Chungbuk, Republic of Korea.
Heejong EomLaboratory Animal Center, Osong Medical Innovation Foundation, Cheongju, Chungbuk, Republic of Korea.
Young Ho KimDepartment of Ophthalmology, Korea University Medicine, Seoul, Republic of Korea.
Cheolmin YunDepartment of Ophthalmology, Korea University Medicine, Seoul, Republic of Korea.
Yong Yeon KimDepartment of Ophthalmology, Korea University Medicine, Seoul, Republic of Korea.
Osong Medical Innovation Foundation · KRKorea University · KRHanoi Medical University · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To investigate responses of macular capillary vessel area density (VAD) of superficial and deep retinal vascular plexuses to elevations in intraocular pressure (IOP) in cynomolgus macaque monkeys using optical coherence tomography angiography (OCTA). Methods: In five general anesthetized male cynomolgus monkeys, the IOP was increased incrementally by 10 mmHg from baseline (10 mmHg) to 70 mmHg and then decreased back to 10 mmHg (recovery state). Structural OCT (30° × 30°) and OCTA (20° × 15°) centered on the macula were obtained at each IOP and 3, 15, and 30 minutes after recovery. En face images of the superficial vascular complex (SVC) and deep vascular complex (DVC) were extracted, and VAD (%) compared with that at baseline was calculated. Results: The VADs in the SVC and DVC at baseline and at 30 mmHg IOP were 34.96%, 34.15%, 35.38%, and 30.12%, respectively. The VAD plateaued until 30 mmHg; however, the VAD was affected more in the DVC than in the SVC (P = 0.008) at 30 mmHg. It showed a significant reduction at 40 mmHg (16.52% SVC, P = 0.006; 18.59% DVC, P = 0.012). In the recovery state, the SVC showed full retention of baseline VAD, but the DVC maintained VAD approximately 70% of that at baseline. Structural OCT showed hyperreflectivity in the nuclear layer, retinal swelling, and an undifferentiated ellipsoid zone from 50 mmHg. Conclusions: Despite physiological autoregulation, perifoveal microcirculation was affected at high IOP ≥ 40 mmHg, especially in the DVC, which explains the pathological mechanism of macular vulnerability in ischemic diseases.

Indexed as

Acute DiseaseAnimalsComputed Tomography AngiographyHomeostasisIntraocular PressureMacaca fascicularisMacula LuteaMaleMicrovesselsOcular HypertensionOptic DiskRetinal VesselsTomography, Optical CoherenceTonometry, Ocular

Identifiers

PMID34932062
PMCPMC8709935
OpenAlexW4200572132

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.