Serum Immunoglobulin G Levels and Nicastrin Variation in Hidradenitis Suppurativa.

IF 11 1区 医学 Q1 DERMATOLOGY JAMA dermatology Pub Date : 2025-04-01 DOI:10.1001/jamadermatol.2024.5684
Dillon Mintoff, Nikolai P Pace
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Abstract

Importance: Variation in nicastrin (NCSTN) is associated with a monogenic subtype of hidradenitis suppurativa. Dysregulation of humoral immunity has been suggested as a potential mechanistic link between NCSTN variation and hidradenitis suppurativa. There is a paucity of biomarkers that can predict disease-associated variation.

Objective: To investigate whether serum immunoglobulin levels, as a surrogate marker of humoral immunity, can identify individuals with hidradenitis suppurativa who have a specific disease-associated NCSTN variant.

Design, setting, and participants: Maltese individuals with hidradenitis suppurativa genotyped for a disease-associated NCSTN in-frame deletion prevalent in the local patient cohort were invited to participate in this cross-sectional study from January to July 2023. Participation was restricted to adult individuals with hidradenitis suppurativa without known or suspected pathologies that would be associated with serum immunoglobulin levels. Data were analyzed between October 2023 and December 2023.

Exposure: Serum immunoglobulin G levels and other hematological paraments were analyzed.

Main outcome and measure: Main outcomes were the associations between serum immunoglobulin levels and an underlying NCSTN variation in individuals with hidradenitis suppurativa.

Results: A total of 125 individuals (64 female individuals [51.2%]) with hidradenitis suppurativa of Maltese ethnicity were recruited in the study, of whom 17 (13.6%) who were from 7 genealogically unrelated families were heterozygous for the disease-associated NCSTN variant. Deletion carriers had a higher serum immunoglobulin G level (1370 mg/dL vs 1140 mg/dL [to convert to g/L, multiply by 0.01]; P < .001). The association between NCSTN variation and elevated immunoglobulin G levels retained significance despite adjusting for multiple confounders, including markers of disease severity, age of recruitment, age of disease onset, treatment with adalimumab, and liver transaminase levels. Serum immunoglobulin G demonstrated a strong discriminatory capacity in identifying patients who were heterozygous for the NCSTN variant.

Conclusion and relevance: The results of this cross-sectional study suggest an altered humoral immune state in patients harboring a specific NCSTN variant and support the role of serum immunoglobulin G levels as a potential predictive biomarker of monogenic hidradenitis suppurativa. This may aid in identifying and prioritizing individuals with monogenic hidradenitis suppurativa.

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化脓性汗腺炎患者血清免疫球蛋白G水平及Nicastrin变化。
重要性:nicastrin (NCSTN)的变异与化脓性汗腺炎的单基因亚型有关。体液免疫失调已被认为是NCSTN变异与化脓性汗腺炎之间的潜在机制联系。目前缺乏能够预测疾病相关变异的生物标志物。目的:探讨血清免疫球蛋白水平作为体液免疫的替代指标,是否能识别化脓性汗腺炎患者是否具有特定疾病相关的NCSTN变异。设计、环境和参与者:马耳他化脓性汗腺炎患者在当地患者队列中普遍存在与疾病相关的NCSTN框架内缺失基因型,被邀请参加这项横断面研究,时间为2023年1月至7月。参与仅限于患有化脓性汗腺炎的成人,没有已知或疑似与血清免疫球蛋白水平相关的病理。数据分析时间为2023年10月至2023年12月。暴露:分析血清免疫球蛋白G水平及其他血液学指标。主要结局和测量:主要结局是化脓性汗腺炎患者血清免疫球蛋白水平与潜在的NCSTN变异之间的关系。结果:研究共招募了125名马耳他种族化脓性汗腺炎患者(64名女性患者[51.2%]),其中17名(13.6%)来自7个无亲缘关系的家族,为该病相关的NCSTN变异杂合。缺失携带者血清免疫球蛋白G水平较高(1370 mg/dL vs 1140 mg/dL[换算成G /L,乘以0.01];结论和相关性:这项横断面研究的结果表明,患有特定NCSTN变异的患者的体液免疫状态发生了改变,并支持血清免疫球蛋白G水平作为单基因化脓性汗腺炎潜在的预测性生物标志物的作用。这可能有助于识别和优先考虑个体与单基因化脓性汗腺炎。
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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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