indotineae 毛癣菌的临床病程、抗真菌敏感性和基因组测序。

IF 11.5 1区 医学 Q1 DERMATOLOGY JAMA dermatology Pub Date : 2024-07-01 DOI:10.1001/jamadermatol.2024.1126
Avrom S Caplan, Gabrielle C Todd, YanChun Zhu, Michelle Sikora, Christine C Akoh, Jeannette Jakus, Shari R Lipner, Kayla Babbush Graber, Karen P Acker, Ayana E Morales, Rebecca M Marrero Rolón, Lars F Westblade, Maira Fonseca, Abigail Cline, Jeremy A W Gold, Shawn R Lockhart, Dallas J Smith, Tom Chiller, William G Greendyke, Swati R Manjari, Nilesh K Banavali, Sudha Chaturvedi
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引用次数: 0

摘要

重要性:indotineae 毛癣菌(Trichophyton indotineae)是一种新出现的皮肤癣菌,可引起大面积癣菌感染,通常对特比萘芬无反应。该物种在全球和美国多个州都有发现,但美国有关吲哚毛癣菌感染的详细数据却很少,而这些数据可以改善治疗方法和医学界对传播的认识:目的:利用全基因组测序技术,将 T indotineae 感染的临床特征与体外抗真菌药敏试验结果、角鲨烯环氧化物酶基因序列变异和分离株亲缘关系联系起来:这项回顾性队列研究的时间跨度为 2022 年 5 月至 2023 年 5 月,研究对象为纽约市的 T indotineae 感染患者。从纽约市的 6 家医疗中心招募了确诊为 T indotineae 感染的患者。主要结果和衡量标准:最后一次随访评估时病情有所改善或缓解:在 11 名 T indotineae 患者中(男性 6 人,女性 5 人;年龄中位数[范围]为 39 [10-65] 岁),2 人怀孕;1 人患有淋巴瘤;其余患者免疫功能正常。九名患者称曾到过孟加拉国。所有患者的皮损范围广泛,鳞屑和炎症程度不一,局部抗真菌单药治疗失败,诊断延误(3-42 个月)。7名患者长期使用标准剂量(每天250毫克)的特比萘芬治疗失败;这些患者的分离物还存在角鲨烯环氧化物酶393位(L393S)或397位(F397L)的氨基酸置换,这与特比萘芬最低抑制浓度升高至0.5微克/毫升或更高有关。接受氟康唑和格列齐特治疗的患者中,分别有 4 例中的 2 例和 5 例中的 2 例病情有所改善,但结果与抗真菌药物最低抑制浓度之间没有关联。此外,在接受伊曲康唑治疗的 7 名患者中,有 5 人在最后一次随访时病情痊愈或好转,7 人中有 2 人失去了随访机会或停止了治疗。根据全基因组测序分析,美国分离株形成了一个有别于印度分离株的群集:本病例系列的结果表明,在这组主要免疫功能正常的趾癣患者中,疾病严重程度、诊断延误以及对治疗趾癣的常用抗真菌药物剂量和疗程缺乏反应的情况很常见,这与已发表的数据一致。伊曲康唑普遍有效,感染可能发生在孟加拉国。
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Clinical Course, Antifungal Susceptibility, and Genomic Sequencing of Trichophyton indotineae.

Importance: Trichophyton indotineae is an emerging dermatophyte causing outbreaks of extensive tinea infections often unresponsive to terbinafine. This species has been detected worldwide and in multiple US states, yet detailed US data on infections with T indotineae are sparse and could improve treatment practices and medical understanding of transmission.

Objective: To correlate clinical features of T indotineae infections with in vitro antifungal susceptibility testing results, squalene epoxidase gene sequence variations, and isolate relatedness using whole-genome sequencing.

Design, setting, and participants: This retrospective cohort study of patients with T indotineae infections in New York City spanned May 2022 to May 2023. Patients with confirmed T indotineae infections were recruited from 6 New York City medical centers.

Main outcome and measure: Improvement or resolution at the last follow-up assessment.

Results: Among 11 patients with T indotineae (6 male and 5 female patients; median [range] age, 39 [10-65] years), 2 were pregnant; 1 had lymphoma; and the remainder were immunocompetent. Nine patients reported previous travel to Bangladesh. All had widespread lesions with variable scale and inflammation, topical antifungal monotherapy failure, and diagnostic delays (range, 3-42 months). Terbinafine treatment failed in 7 patients at standard doses (250 mg daily) for prolonged duration; these patients also had isolates with amino acid substitutions at positions 393 (L393S) or 397 (F397L) in squalene epoxidase that correlated with elevated terbinafine minimum inhibitory concentrations of 0.5 μg/mL or higher. Patients who were treated with fluconazole and griseofulvin improved in 2 of 4 and 2 of 5 instances, respectively, without correlation between outcomes and antifungal minimum inhibitory concentrations. Furthermore, 5 of 7 patients treated with itraconazole cleared or had improvement at the last follow-up, and 2 of 7 were lost to follow-up or stopped treatment. Based on whole-genome sequencing analysis, US isolates formed a cluster distinct from Indian isolates.

Conclusion and relevance: The results of this case series suggest that disease severity, diagnostic delays, and lack of response to typically used doses and durations of antifungals for tinea were common in this primarily immunocompetent patient cohort with T indotineae, consistent with published data. Itraconazole was generally effective, and the acquisition of infection was likely in Bangladesh.

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来源期刊
JAMA dermatology
JAMA dermatology DERMATOLOGY-
CiteScore
14.10
自引率
5.50%
发文量
300
期刊介绍: JAMA Dermatology is an international peer-reviewed journal that has been in continuous publication since 1882. It began publication by the American Medical Association in 1920 as Archives of Dermatology and Syphilology. The journal publishes material that helps in the development and testing of the effectiveness of diagnosis and treatment in medical and surgical dermatology, pediatric and geriatric dermatology, and oncologic and aesthetic dermatologic surgery. JAMA Dermatology is a member of the JAMA Network, a consortium of peer-reviewed, general medical and specialty publications. It is published online weekly, every Wednesday, and in 12 print/online issues a year. The mission of the journal is to elevate the art and science of health and diseases of skin, hair, nails, and mucous membranes, and their treatment, with the aim of enabling dermatologists to deliver evidence-based, high-value medical and surgical dermatologic care. The journal publishes a broad range of innovative studies and trials that shift research and clinical practice paradigms, expand the understanding of the burden of dermatologic diseases and key outcomes, improve the practice of dermatology, and ensure equitable care to all patients. It also features research and opinion examining ethical, moral, socioeconomic, educational, and political issues relevant to dermatologists, aiming to enable ongoing improvement to the workforce, scope of practice, and the training of future dermatologists. JAMA Dermatology aims to be a leader in developing initiatives to improve diversity, equity, and inclusion within the specialty and within dermatology medical publishing.
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