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Geographic Patterns in Psoriasis: An Observational Study of CorEvitas Psoriasis Registry.银屑病的地理分布模式:CorEvitas银屑病登记处的一项观察性研究
J Psoriasis Psoriatic Arthritis. 2022 Jul;7(3):122-131. doi: 10.1177/24755303221081799. Epub 2022 Apr 19.
2
Psoriasis Severity, Comorbidities, and Treatment Response Differ among Geographic Regions in the United States.美国不同地理区域的银屑病严重程度、合并症及治疗反应存在差异。
JID Innov. 2021 May 6;1(2):100025. doi: 10.1016/j.xjidi.2021.100025. eCollection 2021 Jun.
3
Six-Month Real-World Study to Assess the Effectiveness of Ixekizumab After Switching from IL-23 Inhibitors and Other Biologic Therapies: The CorEvitas Psoriasis Registry.一项为期六个月的真实世界研究,旨在评估从白细胞介素-23抑制剂和其他生物疗法转换为司库奇尤单抗后的有效性:CorEvitas银屑病注册研究。
Drugs Real World Outcomes. 2024 Sep;11(3):451-464. doi: 10.1007/s40801-024-00439-w. Epub 2024 Jun 24.
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Skin Clearance is Associated with Reduced Treatment Failure in Patients with Psoriasis: Real-World Evidence from the CorEvitas Psoriasis Registry.皮肤清除与银屑病患者治疗失败率降低相关:来自CorEvitas银屑病登记处的真实世界证据。
Dermatol Ther (Heidelb). 2023 Nov;13(11):2739-2751. doi: 10.1007/s13555-023-01027-6. Epub 2023 Sep 27.
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Comorbid obesity and history of diabetes are independently associated with poorer treatment response to biologics at 6 months: A prospective analysis in Corrona Psoriasis Registry.合并肥胖症和糖尿病史与生物制剂治疗6个月时较差的治疗反应独立相关:来自科罗纳银屑病登记处的前瞻性分析
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Outcomes in Ixekizumab Patients Following Exposure to Secukinumab and Other Biologics in the CorEvitas Psoriasis Registry.在CorEvitas银屑病登记处中接受司库奇尤单抗和其他生物制剂治疗的司库奇尤单抗患者的治疗结果。
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Impact of Disease Burden of Patients with Psoriasis on Biologic Therapy Switching: Real-World Evidence from the CorEvitas Psoriasis Registry.银屑病患者疾病负担对生物制剂治疗转换的影响:来自CorEvitas银屑病登记处的真实世界证据
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本文引用的文献

1
Psoriasis Severity, Comorbidities, and Treatment Response Differ among Geographic Regions in the United States.美国不同地理区域的银屑病严重程度、合并症及治疗反应存在差异。
JID Innov. 2021 May 6;1(2):100025. doi: 10.1016/j.xjidi.2021.100025. eCollection 2021 Jun.
2
Comorbid obesity and history of diabetes are independently associated with poorer treatment response to biologics at 6 months: A prospective analysis in Corrona Psoriasis Registry.合并肥胖症和糖尿病史与生物制剂治疗6个月时较差的治疗反应独立相关:来自科罗纳银屑病登记处的前瞻性分析
J Am Acad Dermatol. 2022 Jan;86(1):68-76. doi: 10.1016/j.jaad.2021.06.883. Epub 2021 Jul 10.
3
Comparison of cumulative clinical benefits of biologics for the treatment of psoriasis over 16 weeks: Results from a network meta-analysis.比较生物制剂治疗银屑病在 16 周以上的累积临床获益:来自网络荟萃分析的结果。
J Am Acad Dermatol. 2020 May;82(5):1138-1149. doi: 10.1016/j.jaad.2019.12.038. Epub 2019 Dec 26.
4
Where you live matters: Regional differences in health care resource use for psoriasis in the United States.居住地很重要:美国银屑病医疗资源使用的地区差异。
J Am Acad Dermatol. 2020 Jun;82(6):1360-1367. doi: 10.1016/j.jaad.2019.10.014. Epub 2019 Oct 10.
5
Trends and Disparities in Asthma Biologic Use in the United States.美国哮喘生物制剂使用的趋势和差异。
J Allergy Clin Immunol Pract. 2020 Feb;8(2):549-554.e1. doi: 10.1016/j.jaip.2019.08.024. Epub 2019 Aug 28.
6
Joint AAD-NPF guidelines of care for the management and treatment of psoriasis with biologics.美国皮肤病学会-银屑病基金会联合指南:生物制剂治疗银屑病的管理与治疗。
J Am Acad Dermatol. 2019 Apr;80(4):1029-1072. doi: 10.1016/j.jaad.2018.11.057. Epub 2019 Feb 13.
7
Joint AAD-NPF guidelines of care for the management and treatment of psoriasis with awareness and attention to comorbidities.联合 AAD-NPF 指南:关注并重视共病,以管理和治疗银屑病。
J Am Acad Dermatol. 2019 Apr;80(4):1073-1113. doi: 10.1016/j.jaad.2018.11.058. Epub 2019 Feb 13.
8
Psoriasis: Which therapy for which patient: Psoriasis comorbidities and preferred systemic agents.银屑病:哪种疗法适合哪种患者:银屑病合并症和首选的系统药物。
J Am Acad Dermatol. 2019 Jan;80(1):27-40. doi: 10.1016/j.jaad.2018.06.057. Epub 2018 Jul 11.
9
Psoriasis: a novel risk factor for type 2 diabetes.银屑病:2型糖尿病的一种新的危险因素。
Lancet Diabetes Endocrinol. 2018 Dec;6(12):919-921. doi: 10.1016/S2213-8587(18)30127-X. Epub 2018 May 21.
10
Metabolic syndrome, C-reactive protein and cardiovascular risk in psoriasis patients: a cross-sectional study.银屑病患者的代谢综合征、C反应蛋白与心血管风险:一项横断面研究
An Bras Dermatol. 2018 Mar;93(2):222-228. doi: 10.1590/abd1806-4841.20186397.

银屑病的地理分布模式:CorEvitas银屑病登记处的一项观察性研究

Geographic Patterns in Psoriasis: An Observational Study of CorEvitas Psoriasis Registry.

作者信息

Enos Clinton W, O'Connell Katie A, Harrison Ryan W, McLean Robert R, Dube Blessing, Van Voorhees Abby S

机构信息

Department of Dermatology, Eastern Virginia Medical School, Norfolk, VA, USA.

CorEvitas, LLC, Waltham, MA, USA.

出版信息

J Psoriasis Psoriatic Arthritis. 2022 Jul;7(3):122-131. doi: 10.1177/24755303221081799. Epub 2022 Apr 19.

DOI:10.1177/24755303221081799
PMID:39296532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11361526/
Abstract

: How psoriasis disease characteristics, management, and outcomes each vary across the US is not fully understood. : Assess regional disease characteristics for patients enrolled in CorEvitas Psoriasis Registry, report biologic initiations by class over the period, and evaluate regional outcome data for initiations with 6-month follow-up. : Participants included new biologic initiations in CorEvitas Psoriasis Registry from 2014-2019 categorized into 7 different geographic regions: Northeast, East North Central, Mountain/West North Central, South Atlantic, East South Central, West South Central, and Pacific. Baseline demographics and disease characteristics are described by region. For participants with 6-month follow-up data, we report treatment patterns and treatment outcomes. : 7520 biologic initiations from 6320 patients were available. Over time, biologic initiations in most US regions within the Registry resulted in a pattern where IL-17 inhibitors were used most frequently, followed by IL-12/23 and IL-23 inhibitors, and lastly by TNF inhibitors. Baseline disease severity varied among regions with the East South Central reporting the largest proportion (25.1%) of very severe disease by body surface area. Frequencies of metabolic comorbid diseases varied between regions (obesity, diabetes, hyperlipidemia, each P < .001; hypertension P < .019), with the East South Central reporting the largest proportions. Rates of achieving PASI75 and IGA 0/1 varied at 6-months (P = .008 and P = .001, respectively), with the East South Central reporting the lowest frequencies. At 6-months 28.2% of biologic initiations in the East South Central were discontinued, of which 22% had switched to another therapy. : Providers should be aware of regional trends in disease characteristics to improve overall care of psoriasis patients.

摘要

目前尚不完全清楚银屑病的疾病特征、治疗方法及治疗结果在美国各地区是如何存在差异的。评估CorEvitas银屑病登记处登记患者的区域疾病特征,报告该时期内各类生物制剂的起始使用情况,并评估起始使用生物制剂且随访6个月的区域治疗结果数据。参与者包括2014年至2019年在CorEvitas银屑病登记处首次使用生物制剂的患者,这些患者被分为7个不同的地理区域:东北部、东中北部、山区/西中北部、南大西洋、东中南部、西中南部和太平洋地区。按区域描述基线人口统计学和疾病特征。对于有6个月随访数据的参与者,我们报告治疗模式和治疗结果。共有来自6320名患者的7520次生物制剂起始使用数据。随着时间推移,登记处内美国大多数地区的生物制剂起始使用呈现出一种模式,即IL-17抑制剂使用最为频繁, 其次是IL-12/23和IL-23抑制剂,最后是TNF抑制剂。各地区基线疾病严重程度有所不同,东中南部报告的体表面积非常严重疾病的比例最高(25.1%)。代谢性合并症的发生率在各地区之间存在差异(肥胖、糖尿病、高脂血症,P均<.001;高血压P <.019),东中南部报告的比例最高。在6个月时达到PASI75和IGA 0/1的比例有所不同(分别为P =.008和P =.001),东中南部报告的频率最低。在6个月时,东中南部28.2%的生物制剂起始使用被停用,其中22%已改用另一种疗法。医疗服务提供者应了解疾病特征的区域趋势,以改善银屑病患者的整体护理。