Genetic diversity of Acanthamoeba and clinical outcome predictors in Danish patients with Acanthamoeba keratitis.

IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Sandra M Skovdal, Christen Rune Stensvold, Henrik Vedel Nielsen, Stine Elkjær Nielsen, Jesper Hjortdal, Anders Ivarsen
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引用次数: 0

Abstract

Purpose: Acanthamoeba keratitis (AK) is a severe corneal infection with potential detrimental effects on visual outcome and quality of life, primarily affecting young contact lens wearers. We report Acanthamoeba genotypes, subtypes and clinical outcome from Danish patients with AK.

Methods: Thirty-nine PCR-positive AK cases diagnosed and treated at Aarhus University Hospital, Denmark, from 2002 to 2022 were included. Corneal samples underwent next-generation sequencing (NGS) for Acanthamoeba genotyping. These data were compared with clinical data and results from PCR.

Results: Acanthamoeba T4 was the most frequent genotype (n = 35), with four subtypes identified (T4A, T4B, T4D and T4G); three cases of the T3 genotype were observed. Three samples showed evidence of two distinct Acanthamoeba sequences. The median patient age was 35 years, genders were equally represented and the median time from symptom onset to diagnosis was 26 days. Ninety per cent had identifiable risk factors in addition to contact lens wear. Corticosteroid treatment prior to AK diagnosis, moderate-to-severe pain, male gender, older age, ring infiltration and infiltrate size >3 mm were associated with poor visual outcome. No significant correlation was found between Acanthamoeba genotype or subtype and clinical outcomes.

Conclusion: We reveal the genetic diversity of Acanthamoeba involved in AK in Denmark. However, genotype or subtype did not predict clinical outcome. Further research is needed to clarify the role of specific genotypes and subtypes in disease progression and treatment response.

丹麦棘阿米巴角膜炎患者棘阿米巴遗传多样性和临床预后预测因素。
目的:棘阿米巴角膜炎(AK)是一种严重的角膜感染,对视力和生活质量有潜在的有害影响,主要影响年轻的隐形眼镜佩戴者。我们报道了丹麦AK患者的棘阿米巴基因型、亚型和临床结果。方法:收集2002 ~ 2022年在丹麦奥胡斯大学医院诊治的39例pcr阳性AK病例。角膜样品进行新一代测序(NGS)进行棘阿米巴基因分型。将临床资料与PCR结果进行比较。结果:棘阿米巴T4是最常见的基因型(n = 35),鉴定出4个亚型(T4A、T4B、T4D和T4G);T3基因型3例。三个样本显示了两种不同棘阿米巴序列的证据。患者中位年龄为35岁,性别平等,从症状发作到诊断的中位时间为26天。除了佩戴隐形眼镜外,90%的人还有可识别的风险因素。AK诊断前皮质类固醇治疗、中度至重度疼痛、男性、年龄较大、环浸润和浸润大小bbb30 mm与视力差有关。棘阿米巴基因型和亚型与临床结果无显著相关性。结论:揭示了与AK相关的棘阿米巴在丹麦的遗传多样性。然而,基因型或亚型并不能预测临床结果。需要进一步的研究来阐明特定基因型和亚型在疾病进展和治疗反应中的作用。
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来源期刊
Acta Ophthalmologica
Acta Ophthalmologica 医学-眼科学
CiteScore
7.60
自引率
5.90%
发文量
433
审稿时长
6 months
期刊介绍: Acta Ophthalmologica is published on behalf of the Acta Ophthalmologica Scandinavica Foundation and is the official scientific publication of the following societies: The Danish Ophthalmological Society, The Finnish Ophthalmological Society, The Icelandic Ophthalmological Society, The Norwegian Ophthalmological Society and The Swedish Ophthalmological Society, and also the European Association for Vision and Eye Research (EVER). Acta Ophthalmologica publishes clinical and experimental original articles, reviews, editorials, educational photo essays (Diagnosis and Therapy in Ophthalmology), case reports and case series, letters to the editor and doctoral theses.
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