预测拉丁美洲系统性红斑狼疮患者严重血小板减少的因素及其对不良预后的影响:来自拉丁美洲多种族队列的数据。

IF 4.6 2区 医学 Q1 RHEUMATOLOGY Seminars in arthritis and rheumatism Pub Date : 2024-10-11 DOI:10.1016/j.semarthrit.2024.152568
Luis Alonso González , Guillermina B. Harvey , Rosana Quintana , Guillermo J. Pons-Estel , Manuel F. Ugarte-Gil , Gloria Vásquez , Luis J Catoggio , Mercedes A. García , Eduardo F. Borba , Nilzio A. Da Silva , João C. Tavares Brenol , Marlene Guibert Toledano , Loreto Massardo , Oscar Neira , Virginia Pascual-Ramos , Mary-Carmen Amigo , Leonor A. Barile-Fabris , Ignacio García De La Torre , José Alfaro-Lozano , María I. Segami , Bernardo A. Pons-Estel
{"title":"预测拉丁美洲系统性红斑狼疮患者严重血小板减少的因素及其对不良预后的影响:来自拉丁美洲多种族队列的数据。","authors":"Luis Alonso González ,&nbsp;Guillermina B. Harvey ,&nbsp;Rosana Quintana ,&nbsp;Guillermo J. Pons-Estel ,&nbsp;Manuel F. Ugarte-Gil ,&nbsp;Gloria Vásquez ,&nbsp;Luis J Catoggio ,&nbsp;Mercedes A. García ,&nbsp;Eduardo F. Borba ,&nbsp;Nilzio A. Da Silva ,&nbsp;João C. Tavares Brenol ,&nbsp;Marlene Guibert Toledano ,&nbsp;Loreto Massardo ,&nbsp;Oscar Neira ,&nbsp;Virginia Pascual-Ramos ,&nbsp;Mary-Carmen Amigo ,&nbsp;Leonor A. Barile-Fabris ,&nbsp;Ignacio García De La Torre ,&nbsp;José Alfaro-Lozano ,&nbsp;María I. Segami ,&nbsp;Bernardo A. Pons-Estel","doi":"10.1016/j.semarthrit.2024.152568","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To examine the predictors of the occurrence of severe thrombocytopenia and its impact on damage accrual and mortality in SLE patients.</div></div><div><h3>Methods</h3><div>Factors associated with time to severe thrombocytopenia (platelet count ≤20,000/mm<sup>3</sup>) occurring from the onset of SLE symptoms were assessed by Cox proportional hazards regressions. The association of severe thrombocytopenia with mortality was evaluated by logistic regression analyses while its impact on damage was by negative binomial regression.</div></div><div><h3>Results</h3><div>Of 1,217 patients, 33 (2.7%) developed severe thrombocytopenia over a mean (SD) follow-up time of 5.9 (3.6) years. The median time from the onset of SLE symptoms to severe thrombocytopenia occurrence was 22 months (IQR 8.7–62.0). Mestizo (60.6%) was the predominant ethnic group, followed by Caucasian (27.3%), while African Latin American exhibited the lowest frequency (12.1%). By multivariable analysis, Mestizo ethnicity (HR 2.67, 95% CI 1.12–6.37, <em>p</em> = 0.027), and autoimmune hemolytic anemia (AIHA) at baseline (HR 3.99; 95% CI 1.05–15.19, <em>p</em> = 0.042) were associated with a shorter time to the occurrence of severe thrombocytopenia while middle/high socioeconomic status (HR 0.23; 95% CI 0.08–0.69, <em>p</em> = 0.008) was associated with a longer time. Severe thrombocytopenia contributed neither to damage nor to mortality.</div></div><div><h3>Conclusions</h3><div>Severe thrombocytopenia occurs during the early course of SLE. Mestizo ethnicity and AIHA at baseline emerged as independent predictors of a shorter time to severe thrombocytopenia occurrence while a middle/high socioeconomic status seems to be protective against its occurrence. Damage and mortality did not seem to be impacted by the occurrence of severe thrombocytopenia.</div></div>","PeriodicalId":21715,"journal":{"name":"Seminars in arthritis and rheumatism","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Factors predictive of severe thrombocytopenia and its impact on poor outcomes in Latin American patients with systemic lupus erythematosus: Data from a multiethnic Latin American cohort\",\"authors\":\"Luis Alonso González ,&nbsp;Guillermina B. Harvey ,&nbsp;Rosana Quintana ,&nbsp;Guillermo J. Pons-Estel ,&nbsp;Manuel F. Ugarte-Gil ,&nbsp;Gloria Vásquez ,&nbsp;Luis J Catoggio ,&nbsp;Mercedes A. García ,&nbsp;Eduardo F. Borba ,&nbsp;Nilzio A. Da Silva ,&nbsp;João C. Tavares Brenol ,&nbsp;Marlene Guibert Toledano ,&nbsp;Loreto Massardo ,&nbsp;Oscar Neira ,&nbsp;Virginia Pascual-Ramos ,&nbsp;Mary-Carmen Amigo ,&nbsp;Leonor A. Barile-Fabris ,&nbsp;Ignacio García De La Torre ,&nbsp;José Alfaro-Lozano ,&nbsp;María I. Segami ,&nbsp;Bernardo A. Pons-Estel\",\"doi\":\"10.1016/j.semarthrit.2024.152568\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>To examine the predictors of the occurrence of severe thrombocytopenia and its impact on damage accrual and mortality in SLE patients.</div></div><div><h3>Methods</h3><div>Factors associated with time to severe thrombocytopenia (platelet count ≤20,000/mm<sup>3</sup>) occurring from the onset of SLE symptoms were assessed by Cox proportional hazards regressions. The association of severe thrombocytopenia with mortality was evaluated by logistic regression analyses while its impact on damage was by negative binomial regression.</div></div><div><h3>Results</h3><div>Of 1,217 patients, 33 (2.7%) developed severe thrombocytopenia over a mean (SD) follow-up time of 5.9 (3.6) years. The median time from the onset of SLE symptoms to severe thrombocytopenia occurrence was 22 months (IQR 8.7–62.0). Mestizo (60.6%) was the predominant ethnic group, followed by Caucasian (27.3%), while African Latin American exhibited the lowest frequency (12.1%). By multivariable analysis, Mestizo ethnicity (HR 2.67, 95% CI 1.12–6.37, <em>p</em> = 0.027), and autoimmune hemolytic anemia (AIHA) at baseline (HR 3.99; 95% CI 1.05–15.19, <em>p</em> = 0.042) were associated with a shorter time to the occurrence of severe thrombocytopenia while middle/high socioeconomic status (HR 0.23; 95% CI 0.08–0.69, <em>p</em> = 0.008) was associated with a longer time. Severe thrombocytopenia contributed neither to damage nor to mortality.</div></div><div><h3>Conclusions</h3><div>Severe thrombocytopenia occurs during the early course of SLE. Mestizo ethnicity and AIHA at baseline emerged as independent predictors of a shorter time to severe thrombocytopenia occurrence while a middle/high socioeconomic status seems to be protective against its occurrence. Damage and mortality did not seem to be impacted by the occurrence of severe thrombocytopenia.</div></div>\",\"PeriodicalId\":21715,\"journal\":{\"name\":\"Seminars in arthritis and rheumatism\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Seminars in arthritis and rheumatism\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0049017224002087\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminars in arthritis and rheumatism","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0049017224002087","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

目的研究严重血小板减少症发生的预测因素及其对系统性红斑狼疮患者损伤累积和死亡率的影响:方法:采用Cox比例危险度回归法评估从系统性红斑狼疮症状开始到发生严重血小板减少(血小板计数≤20,000/mm3)的时间相关因素。严重血小板减少症与死亡率的关系通过逻辑回归分析进行评估,而其对损害的影响则通过负二项回归进行评估:在 1217 名患者中,33 人(2.7%)在平均(标度)5.9(3.6)年的随访时间内出现了严重血小板减少症。从出现系统性红斑狼疮症状到出现严重血小板减少症的中位时间为 22 个月(IQR 8.7-62.0)。梅斯蒂索人(60.6%)是主要的种族群体,其次是白种人(27.3%),而非洲裔拉美人的发病率最低(12.1%)。通过多变量分析,梅斯蒂索种族(HR 2.67,95% CI 1.12-6.37,p = 0.027)和基线时的自身免疫性溶血性贫血(AIHA)(HR 3.99;95% CI 1.05-15.19,p = 0.042)与患者的寿命缩短有关。042)与较短的严重血小板减少症发生时间相关,而中/高社会经济地位(HR 0.23;95% CI 0.08-0.69,p = 0.008)与较长的时间相关。严重血小板减少既不会造成损害,也不会导致死亡:结论:严重血小板减少症发生在系统性红斑狼疮的早期。结论:严重血小板减少症发生在系统性红斑狼疮的早期病程中。梅斯蒂索种族和基线时的AIHA是预测严重血小板减少症发生时间缩短的独立因素,而中/高社会经济地位似乎对严重血小板减少症的发生具有保护作用。损害和死亡率似乎不受严重血小板减少症发生的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Factors predictive of severe thrombocytopenia and its impact on poor outcomes in Latin American patients with systemic lupus erythematosus: Data from a multiethnic Latin American cohort

Objective

To examine the predictors of the occurrence of severe thrombocytopenia and its impact on damage accrual and mortality in SLE patients.

Methods

Factors associated with time to severe thrombocytopenia (platelet count ≤20,000/mm3) occurring from the onset of SLE symptoms were assessed by Cox proportional hazards regressions. The association of severe thrombocytopenia with mortality was evaluated by logistic regression analyses while its impact on damage was by negative binomial regression.

Results

Of 1,217 patients, 33 (2.7%) developed severe thrombocytopenia over a mean (SD) follow-up time of 5.9 (3.6) years. The median time from the onset of SLE symptoms to severe thrombocytopenia occurrence was 22 months (IQR 8.7–62.0). Mestizo (60.6%) was the predominant ethnic group, followed by Caucasian (27.3%), while African Latin American exhibited the lowest frequency (12.1%). By multivariable analysis, Mestizo ethnicity (HR 2.67, 95% CI 1.12–6.37, p = 0.027), and autoimmune hemolytic anemia (AIHA) at baseline (HR 3.99; 95% CI 1.05–15.19, p = 0.042) were associated with a shorter time to the occurrence of severe thrombocytopenia while middle/high socioeconomic status (HR 0.23; 95% CI 0.08–0.69, p = 0.008) was associated with a longer time. Severe thrombocytopenia contributed neither to damage nor to mortality.

Conclusions

Severe thrombocytopenia occurs during the early course of SLE. Mestizo ethnicity and AIHA at baseline emerged as independent predictors of a shorter time to severe thrombocytopenia occurrence while a middle/high socioeconomic status seems to be protective against its occurrence. Damage and mortality did not seem to be impacted by the occurrence of severe thrombocytopenia.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
9.20
自引率
4.00%
发文量
176
审稿时长
46 days
期刊介绍: Seminars in Arthritis and Rheumatism provides access to the highest-quality clinical, therapeutic and translational research about arthritis, rheumatology and musculoskeletal disorders that affect the joints and connective tissue. Each bimonthly issue includes articles giving you the latest diagnostic criteria, consensus statements, systematic reviews and meta-analyses as well as clinical and translational research studies. Read this journal for the latest groundbreaking research and to gain insights from scientists and clinicians on the management and treatment of musculoskeletal and autoimmune rheumatologic diseases. The journal is of interest to rheumatologists, orthopedic surgeons, internal medicine physicians, immunologists and specialists in bone and mineral metabolism.
期刊最新文献
Real-world assessment of the efficacy and tolerability profile of JAK inhibitors in difficult-to-treat rheumatoid arthritis Systematic review of treatments for the gastrointestinal manifestations of systemic lupus erythematosus Primary headache in SLE –systematic review and meta-analysis Information and communication technology-based patient education for autoimmune inflammatory rheumatic diseases: A scoping review Improvement in spinal pain at night and its impact on long-term outcomes in radiographic axial spondyloarthritis: Results from Ixekizumab COAST-V randomised trial
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1