• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Machine Learning-Based Deep Phenotyping of Atopic Dermatitis: Severity-Associated Factors in Adolescent and Adult Patients.基于机器学习的特应性皮炎深度表型分析:青少年和成年患者严重程度相关因素。
JAMA Dermatol. 2021 Dec 1;157(12):1414-1424. doi: 10.1001/jamadermatol.2021.3668.
2
Phenotypical Differences of Childhood- and Adult-Onset Atopic Dermatitis.儿童期和成人期特应性皮炎的表型差异。
J Allergy Clin Immunol Pract. 2018 Jul-Aug;6(4):1306-1312. doi: 10.1016/j.jaip.2017.10.005. Epub 2017 Nov 10.
3
Association of Adult Atopic Dermatitis Severity With Decreased Physical Activity: A Cross-sectional Study.成人特应性皮炎严重程度与体力活动减少的相关性:一项横断面研究。
Dermatitis. 2023 May-Jun;34(3):218-223. doi: 10.1097/DER.0000000000000921. Epub 2023 Jan 2.
4
Association of Adult Atopic Dermatitis Severity With Bacterial, Viral, and Fungal Skin Infections.成人特应性皮炎严重程度与细菌性、病毒性和真菌性皮肤感染的关联。
Dermatitis. 2023 Mar-Apr;34(2):120-126. doi: 10.1089/derm.2022.29006.jrd. Epub 2023 Jan 19.
5
The Influence of Atopic Dermatitis on Health-Related Quality of Life in Bangladesh.特应性皮炎对孟加拉国健康相关生活质量的影响。
Int J Environ Res Public Health. 2021 Nov 4;18(21):11593. doi: 10.3390/ijerph182111593.
6
Severity strata for Eczema Area and Severity Index (EASI), modified EASI, Scoring Atopic Dermatitis (SCORAD), objective SCORAD, Atopic Dermatitis Severity Index and body surface area in adolescents and adults with atopic dermatitis.特应性皮炎青少年和成人患者的湿疹面积和严重程度指数(EASI)、改良 EASI、特应性皮炎评分(SCORAD)、客观 SCORAD、特应性皮炎严重程度指数和体表面积严重程度分层。
Br J Dermatol. 2017 Nov;177(5):1316-1321. doi: 10.1111/bjd.15641. Epub 2017 Oct 1.
7
The risk factors for food allergy in infants with atopic dermatitis.特应性皮炎婴儿食物过敏的危险因素。
Turk J Pediatr. 2023;65(2):235-244. doi: 10.24953/turkjped.2022.656.
8
Prevalence and associations of fatigue in childhood atopic dermatitis: A cross-sectional study.儿童特应性皮炎疲劳的患病率及其相关性:一项横断面研究。
J Eur Acad Dermatol Venereol. 2023 Apr;37(4):763-771. doi: 10.1111/jdv.18819. Epub 2023 Jan 4.
9
Long-Term Efficacy and Safety of Dupilumab in Adolescents with Moderate-to-Severe Atopic Dermatitis: Results Through Week 52 from a Phase III Open-Label Extension Trial (LIBERTY AD PED-OLE).度普利尤单抗治疗青少年中重度特应性皮炎的长期疗效和安全性:III 期开放标签扩展试验(LIBERTY AD PED-OLE)的第 52 周结果。
Am J Clin Dermatol. 2022 May;23(3):365-383. doi: 10.1007/s40257-022-00683-2. Epub 2022 May 14.
10
Clinical phenotyping of atopic dermatitis using combined itch and lesional severity: A prospective observational study.采用联合瘙痒和皮损严重程度对特应性皮炎进行临床表型分析:一项前瞻性观察研究。
Ann Allergy Asthma Immunol. 2021 Jul;127(1):83-90.e2. doi: 10.1016/j.anai.2021.03.019. Epub 2021 Apr 2.

引用本文的文献

1
The construction of HMME-PDT efficacy prediction model for port-wine stain based on machine learning algorithms.基于机器学习算法的鲜红斑痣光动力疗法疗效预测模型构建。
Sci Rep. 2025 Jul 2;15(1):22563. doi: 10.1038/s41598-025-06589-3.
2
Machine learning-based prediction models for atopic dermatitis diagnosis and evaluation.基于机器学习的特应性皮炎诊断与评估预测模型
Fundam Res. 2023 Mar 21;5(3):1313-1322. doi: 10.1016/j.fmre.2023.02.021. eCollection 2025 May.
3
Artificial intelligence-enabled precision medicine for inflammatory skin diseases.用于炎症性皮肤病的人工智能精准医学。
ArXiv. 2025 May 14:arXiv:2505.09527v1.
4
Application and research progress of artificial intelligence in allergic diseases.人工智能在过敏性疾病中的应用与研究进展
Int J Med Sci. 2025 Apr 9;22(9):2088-2102. doi: 10.7150/ijms.105422. eCollection 2025.
5
Advancements in artificial intelligence for atopic dermatitis: diagnosis, treatment, and patient management.人工智能在特应性皮炎中的进展:诊断、治疗及患者管理
Ann Med. 2025 Dec;57(1):2484665. doi: 10.1080/07853890.2025.2484665. Epub 2025 Apr 8.
6
Identification and Validation of the Potential Key Biomarkers for Atopic Dermatitis Mitochondrion by Learning Algorithms.通过学习算法鉴定和验证特应性皮炎线粒体的潜在关键生物标志物
J Inflamm Res. 2025 Mar 21;18:4291-4306. doi: 10.2147/JIR.S507085. eCollection 2025.
7
Patient Needs and Treatment Goals in Chronic Atopic Pruritus: Does Eczema Make a Difference?慢性特应性瘙痒中的患者需求与治疗目标:湿疹有影响吗?
Acta Derm Venereol. 2025 Mar 12;105:adv42773. doi: 10.2340/actadv.v105.42773.
8
Utilization of Computable Phenotypes in Electronic Health Record Research: A Review and Case Study in Atopic Dermatitis.电子健康记录研究中可计算表型的应用:以特应性皮炎为例的综述与案例研究
J Invest Dermatol. 2025 May;145(5):1008-1016. doi: 10.1016/j.jid.2024.08.025. Epub 2024 Nov 1.
9
Digital twins in dermatology, current status, and the road ahead.皮肤病学中的数字孪生、现状及未来之路。
NPJ Digit Med. 2024 Aug 26;7(1):228. doi: 10.1038/s41746-024-01220-7.
10
Genomic and functional divergence of strains from atopic dermatitis patients and healthy individuals: insights from global and local scales.来自特应性皮炎患者和健康个体的 菌株的基因组和功能分化:从全球和局部尺度获得的见解。
Microbiol Spectr. 2024 Oct 3;12(10):e0057124. doi: 10.1128/spectrum.00571-24. Epub 2024 Aug 20.

基于机器学习的特应性皮炎深度表型分析:青少年和成年患者严重程度相关因素。

Machine Learning-Based Deep Phenotyping of Atopic Dermatitis: Severity-Associated Factors in Adolescent and Adult Patients.

机构信息

Department of Dermatology and Allergy, University Hospital Bonn, Venusberg-Campus 1, Germany.

Christine Kühne-Center for Allergy Research and Education Davos (CK-CARE), Davos, Switzerland.

出版信息

JAMA Dermatol. 2021 Dec 1;157(12):1414-1424. doi: 10.1001/jamadermatol.2021.3668.

DOI:10.1001/jamadermatol.2021.3668
PMID:34757407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8581798/
Abstract

IMPORTANCE

Atopic dermatitis (AD) is the most common chronic inflammatory skin disease and is driven by a complex pathophysiology underlying highly heterogeneous phenotypes. Current advances in precision medicine emphasize the need for stratification.

OBJECTIVE

To perform deep phenotyping and identification of severity-associated factors in adolescent and adult patients with AD.

DESIGN, SETTING, AND PARTICIPANTS: Cross-sectional data from the baseline visit of a prospective longitudinal study investigating the phenotype among inpatients and outpatients with AD from the Department of Dermatology and Allergy of the University Hospital Bonn enrolled between November 2016 and February 2020.

MAIN OUTCOMES AND MEASURES

Patients were stratified by severity groups using the Eczema Area and Severity Index (EASI). The associations of 130 factors with AD severity were analyzed applying a machine learning-gradient boosting approach with cross-validation-based tuning as well as multinomial logistic regression.

RESULTS

A total of 367 patients (157 male [42.8%]; mean [SD] age, 39 [17] years; 94% adults) were analyzed. Among the participants, 177 (48.2%) had mild disease (EASI ≤7), 120 (32.7%) had moderate disease (EASI >7 and ≤ 21), and 70 (19.1%) had severe disease (EASI >21). Atopic stigmata (cheilitis: odds ratio [OR], 8.10; 95% CI, 3.35-10.59; white dermographism: OR, 4.42; 95% CI, 1.68-11.64; Hertoghe sign: OR, 2.75; 95% CI, 1.27-5.93; nipple eczema: OR, 4.97; 95% CI, 1.56-15.78) was associated with increased probability of severe AD, while female sex was associated with reduced probability (OR, 0.30; 95% CI, 0.13-0.66). The probability of severe AD was associated with total serum immunoglobulin E levels greater than 1708 IU/mL and eosinophil values greater than 6.8%. Patients aged 12 to 21 years or older than 52 years had an elevated probability of severe AD; patients aged 22 to 51 years had an elevated probability of mild AD. Age at AD onset older than 12 years was associated with increased probability of severe AD up to a peak at 30 years; age at onset older than 33 years was associated with moderate to severe AD; and childhood onset was associated with mild AD (peak, 7 years). Lifestyle factors associated with severe AD were physical activity less than once per week and (former) smoking. Alopecia areata was associated with moderate (OR, 5.23; 95% CI, 1.53-17.88) and severe (OR, 4.67; 95% CI, 1.01-21.56) AD. Predictive performance of machine learning-gradient boosting vs multinomial logistic regression differed only slightly (mean multiclass area under the curve value: 0.71 [95% CI, 0.69-0.72] vs 0.68 [0.66-0.70], respectively).

CONCLUSIONS AND RELEVANCE

The associations found in this cross-sectional study among patients with AD might contribute to a deeper disease understanding, closer monitoring of predisposed patients, and personalized prevention and therapy.

摘要

重要性

特应性皮炎(AD)是最常见的慢性炎症性皮肤病,其病理生理学基础复杂,表型高度异质。当前精准医学的进展强调了分层的必要性。

目的

对青少年和成年 AD 患者进行深度表型分析,并确定与严重程度相关的因素。

设计、地点和参与者:这是一项横断面研究,从 2016 年 11 月至 2020 年 2 月,在波恩大学医院皮肤科和过敏科招募了门诊和住院 AD 患者的前瞻性纵向研究的基线访视中收集了横断面数据。

主要结局和测量

使用 Eczema Area and Severity Index(EASI)对患者进行严重程度分组。应用机器学习梯度提升方法结合基于交叉验证的调优以及多项逻辑回归分析了 130 个因素与 AD 严重程度的关联。

结果

共分析了 367 例患者(男性 157 例[42.8%];平均[标准差]年龄 39[17]岁;94%为成年人)。参与者中,177 例(48.2%)为轻度疾病(EASI≤7),120 例(32.7%)为中度疾病(EASI>7 且≤21),70 例(19.1%)为重度疾病(EASI>21)。特应性标志(唇炎:比值比[OR],8.10;95%置信区间[CI],3.35-10.59;白色划痕症:OR,4.42;95%CI,1.68-11.64;Hertoghe 征:OR,2.75;95%CI,1.27-5.93;乳头湿疹:OR,4.97;95%CI,1.56-15.78)与严重 AD 的概率增加相关,而女性与概率降低相关(OR,0.30;95%CI,0.13-0.66)。总血清免疫球蛋白 E 水平大于 1708 IU/mL 和嗜酸性粒细胞值大于 6.8%与严重 AD 的概率相关。12 至 21 岁或 52 岁以上的患者发生严重 AD 的概率增加;22 至 51 岁的患者发生轻度 AD 的概率增加。AD 发病年龄大于 12 岁与严重 AD 的概率增加相关,峰值出现在 30 岁;发病年龄大于 33 岁与中重度 AD 相关;儿童发病与轻度 AD 相关(峰值为 7 岁)。与严重 AD 相关的生活方式因素是每周运动次数少于一次和(曾)吸烟。斑秃与中度(OR,5.23;95%CI,1.53-17.88)和重度(OR,4.67;95%CI,1.01-21.56)AD 相关。机器学习梯度提升与多项逻辑回归的预测性能差异仅略有不同(平均多类曲线下面积值:0.71[95%CI,0.69-0.72]与 0.68[0.66-0.70])。

结论和相关性

本研究在 AD 患者中发现的关联可能有助于更深入地了解疾病,对易患患者进行更密切的监测,并进行个性化的预防和治疗。