• 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
Brief Report: Sex Differences in Outcomes for Individuals Presenting for Third-Line Antiretroviral Therapy.简要报告:第三线抗逆转录病毒治疗患者的结局中的性别差异。
J Acquir Immune Defic Syndr. 2020 Jun 1;84(2):203-207. doi: 10.1097/QAI.0000000000002324.
2
Third-line antiretroviral therapy in low-income and middle-income countries (ACTG A5288): a prospective strategy study.中低收入国家的三线抗逆转录病毒治疗(ACTG A5288):一项前瞻性策略研究。
Lancet HIV. 2019 Sep;6(9):e588-e600. doi: 10.1016/S2352-3018(19)30146-8. Epub 2019 Jul 29.
3
Nevirapine- versus lopinavir/ritonavir-based initial therapy for HIV-1 infection among women in Africa: a randomized trial.奈韦拉平与洛匹那韦/利托那韦初始治疗方案用于非洲女性人类免疫缺陷病毒 1 型感染:一项随机试验。
PLoS Med. 2012;9(6):e1001236. doi: 10.1371/journal.pmed.1001236. Epub 2012 Jun 12.
4
Third-line antiretroviral therapy, including raltegravir (RAL), darunavir (DRV/r) and/or etravirine (ETR), is well tolerated and achieves durable virologic suppression over 144 weeks in resource-limited settings: ACTG A5288 strategy trial.三线抗反转录病毒治疗,包括拉替拉韦(RAL)、达芦那韦(DRV/r)和/或依曲韦林(ETR),在资源有限的环境中具有良好的耐受性,并在 144 周以上实现持久的病毒学抑制:ACTG A5288 策略试验。
J Int AIDS Soc. 2022 Jun;25(6):e25905. doi: 10.1002/jia2.25905.
5
Virologic and immunologic outcomes of HIV-infected Ugandan children randomized to lopinavir/ritonavir or nonnucleoside reverse transcriptase inhibitor therapy.随机分配接受洛匹那韦/利托那韦或非核苷类逆转录酶抑制剂治疗的感染 HIV 的乌干达儿童的病毒学和免疫学结局。
J Acquir Immune Defic Syndr. 2014 Apr 15;65(5):535-41. doi: 10.1097/QAI.0000000000000071.
6
Body composition and metabolic outcomes after 96 weeks of treatment with ritonavir-boosted lopinavir plus either nucleoside or nucleotide reverse transcriptase inhibitors or raltegravir in patients with HIV with virological failure of a standard first-line antiretroviral therapy regimen: a substudy of the randomised, open-label, non-inferiority SECOND-LINE study.在标准一线抗逆转录病毒治疗方案失败的 HIV 患者中,经过 96 周利托那韦增强洛匹那韦加核苷或核苷酸逆转录酶抑制剂或拉替拉韦治疗后的身体成分和代谢结果:一项随机、开放标签、非劣效性 SECOND-LINE 研究的子研究。
Lancet HIV. 2017 Jan;4(1):e13-e20. doi: 10.1016/S2352-3018(16)30189-8. Epub 2016 Nov 1.
7
Diverse Human Immunodeficiency Virus-1 Drug Resistance Profiles at Screening for ACTG A5288: A Study of People Experiencing Virologic Failure on Second-line Antiretroviral Therapy in Resource-limited Settings.在 ACTG A5288 研究中对资源有限环境下二线抗逆转录病毒治疗失败的人群进行病毒学筛查时,出现了多种人类免疫缺陷病毒-1 耐药性特征。
Clin Infect Dis. 2020 Oct 23;71(7):e170-e177. doi: 10.1093/cid/ciz1116.
8
Randomized open-label trial of two simplified, class-sparing regimens following a first suppressive three or four-drug regimen.在首个采用三种或四种药物的抑制性治疗方案之后,对两种简化的、保留类别治疗方案进行的随机开放标签试验。
AIDS. 2007 Jan 30;21(3):325-33. doi: 10.1097/QAD.0b013e328011ddfa.
9
Examination of noninferiority, safety, and tolerability of lopinavir/ritonavir and raltegravir compared with lopinavir/ritonavir and tenofovir/ emtricitabine in antiretroviral-naïve subjects: the progress study, 48-week results.在初治抗逆转录病毒治疗受试者中比较洛匹那韦/利托那韦与拉替拉韦以及洛匹那韦/利托那韦与替诺福韦/恩曲他滨的非劣效性、安全性和耐受性:进展研究,48周结果
HIV Clin Trials. 2011 Sep-Oct;12(5):255-67. doi: 10.1310/hct1205-255.
10
Efavirenz-based simplification after successful early lopinavir-boosted-ritonavir-based therapy in HIV-infected children in Burkina Faso and Côte d'Ivoire: the MONOD ANRS 12206 non-inferiority randomised trial.布基纳法索和科特迪瓦艾滋病毒感染儿童在基于洛匹那韦增强型利托那韦的早期治疗成功后基于依非韦伦的简化治疗:MONOD ANRS 12206非劣效性随机试验
BMC Med. 2017 Apr 24;15(1):85. doi: 10.1186/s12916-017-0842-4.

引用本文的文献

1
Viral load suppression rate of third-line antiretroviral therapy and its association with gender among HIV patients after second-line treatment failure in Africa: a systematic review and meta-analysis.非洲二线治疗失败后HIV患者的三线抗逆转录病毒治疗病毒载量抑制率及其与性别的关联:一项系统评价和荟萃分析
BMC Infect Dis. 2025 Feb 3;25(1):158. doi: 10.1186/s12879-025-10576-4.
2
Treatment Outcomes After Switching to Second-Line Anti-Retroviral Therapy: Results From the Thai National Treatment Program.二线抗逆转录病毒治疗转换后的治疗结局:来自泰国国家治疗项目的结果。
J Int Assoc Provid AIDS Care. 2023 Jan-Dec;22:23259582231220513. doi: 10.1177/23259582231220513.
3
Predictors of virologic outcome among people living with HIV who continue a protease inhibitor-based antiretroviral regimen following virologic failure with no or limited resistance.在没有或有限耐药的情况下,经病毒学失败后继续使用基于蛋白酶抑制剂的抗逆转录病毒治疗方案的 HIV 感染者的病毒学结局预测因素。
AIDS Res Ther. 2023 Jan 5;20(1):3. doi: 10.1186/s12981-022-00494-9.
4
Multilevel Analysis of Individual and Neighborhood Characteristics Associated with Viral Suppression Among Adults with HIV in Rio de Janeiro, Brazil.巴西里约热内卢成年人 HIV 病毒抑制与个体和社区特征的多水平分析。
AIDS Behav. 2022 Mar;26(3):947-962. doi: 10.1007/s10461-021-03450-2. Epub 2021 Sep 25.
5
Evaluating Quality of Life and Marital Contentment among Seroconcordant and Serodiscordant HIV-Infected Couples in Comparison to Non- HIV Couples.与未感染艾滋病毒的夫妇相比,评估血清学一致和血清学不一致的艾滋病毒感染夫妇的生活质量和婚姻满意度。
Int J Community Based Nurs Midwifery. 2021 Jul;9(3):251-264. doi: 10.30476/ijcbnm.2021.87420.1430.
6
Where are we with understanding of COVID-19?我们对新冠病毒的了解处于什么程度?
Adv Biol Regul. 2020 Dec;78:100738. doi: 10.1016/j.jbior.2020.100738. Epub 2020 Jun 20.
7
Where are we with understanding of COVID-19?我们对新冠病毒的了解处于什么程度?
Adv Biol Regul. 2020 Aug;77:100745. doi: 10.1016/j.jbior.2020.100745. Epub 2020 Jul 21.

本文引用的文献

1
Third-line antiretroviral therapy in low-income and middle-income countries (ACTG A5288): a prospective strategy study.中低收入国家的三线抗逆转录病毒治疗(ACTG A5288):一项前瞻性策略研究。
Lancet HIV. 2019 Sep;6(9):e588-e600. doi: 10.1016/S2352-3018(19)30146-8. Epub 2019 Jul 29.
2
Outcomes by sex following treatment initiation with atazanavir plus ritonavir or efavirenz with abacavir/lamivudine or tenofovir/emtricitabine.使用阿扎那韦加利托那韦或依非韦伦与阿巴卡韦/拉米夫定或替诺福韦/恩曲他滨联合治疗开始后的性别相关结果。
Clin Infect Dis. 2014 Feb;58(4):555-63. doi: 10.1093/cid/cit747. Epub 2013 Nov 18.
3
Women and men report different behaviours in, and reasons for medication non-adherence: a nationwide Swedish survey.女性和男性报告了在药物治疗不依从方面的不同行为及原因:一项瑞典全国性调查。
Pharm Pract (Granada). 2012 Oct;10(4):207-21. doi: 10.4321/s1886-36552012000400005. Epub 2012 Dec 31.
4
Outcomes for efavirenz versus nevirapine-containing regimens for treatment of HIV-1 infection: a systematic review and meta-analysis.依非韦伦与含奈韦拉平方案治疗人类免疫缺陷病毒 1 型感染的结局:系统评价和荟萃分析。
PLoS One. 2013 Jul 22;8(7):e68995. doi: 10.1371/journal.pone.0068995. Print 2013.
5
Virologic failure of protease inhibitor-based second-line antiretroviral therapy without resistance in a large HIV treatment program in South Africa.在南非一个大型艾滋病毒治疗项目中,基于蛋白酶抑制剂的二线抗逆转录病毒治疗在无耐药情况下出现病毒学失败。
PLoS One. 2012;7(3):e32144. doi: 10.1371/journal.pone.0032144. Epub 2012 Mar 13.
6
Sex differences in lopinavir and ritonavir pharmacokinetics among HIV-infected women and men.HIV 感染者中洛匹那韦和利托那韦的药代动力学的性别差异。
J Clin Pharmacol. 2011 Dec;51(12):1665-73. doi: 10.1177/0091270010388650. Epub 2011 Jan 13.
7
Comparative gender analysis of the efficacy and safety of atazanavir/ritonavir and lopinavir/ritonavir at 96 weeks in the CASTLE study.CASTLE 研究中,在第 96 周时比较阿扎那韦/利托那韦与洛匹那韦/利托那韦的疗效和安全性的性别分析。
J Antimicrob Chemother. 2011 Feb;66(2):363-70. doi: 10.1093/jac/dkq457. Epub 2010 Dec 9.
8
Sex-based outcomes of darunavir-ritonavir therapy: a single-group trial.达芦那韦利托那韦治疗的基于性别的结局:一项单组试验。
Ann Intern Med. 2010 Sep 21;153(6):349-57. doi: 10.7326/0003-4819-153-6-201009210-00002.
9
Does gender and nevirapine (NVP) influence abnormal liver functions in HIV disease?性别和奈韦拉平(NVP)是否会影响HIV疾病中的肝功能异常?
J Infect. 2009 Mar;58(3):255-7. doi: 10.1016/j.jinf.2009.01.003. Epub 2009 Feb 7.
10
Antiretroviral pharmacokinetic profile: a review of sex differences.抗逆转录病毒药物的药代动力学概况:性别差异综述
Gend Med. 2007 Jun;4(2):106-19. doi: 10.1016/s1550-8579(07)80025-8.

简要报告:第三线抗逆转录病毒治疗患者的结局中的性别差异。

Brief Report: Sex Differences in Outcomes for Individuals Presenting for Third-Line Antiretroviral Therapy.

机构信息

Division of AIDS NIAID, NIH, Bethesda, MD.

Harvard T.H. Chan School of Public Health, Boston, MA.

出版信息

J Acquir Immune Defic Syndr. 2020 Jun 1;84(2):203-207. doi: 10.1097/QAI.0000000000002324.

DOI:10.1097/QAI.0000000000002324
PMID:32049773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7228852/
Abstract

BACKGROUND

Sex differences in studies of antiretroviral (ART) drug exposure and treatment outcomes support the hypothesis that some ART combinations may not be well tolerated in women. We evaluated disparities in outcomes between men and women participating in ACTG A5288, an interventional strategy trial for individuals failing a protease inhibitor-based second-line ART regimen in low- and middle-income countries.

METHODS

Participants were assigned to one of 4 cohorts (A-D) based on resistance profiles and ART history. Cohort A had no lopinavir/ritonavir (LPV/r) resistance and stayed on their second-line regimen, and cohorts B, C, and D had increasing resistance and accessed novel ART regimens. In this secondary analysis, we evaluated sex differences in the primary endpoint, HIV-1 RNA ≤200 copies/mL at week 48; confirmed virologic failure ≥1000 copies/mL (VF); and clinical outcomes and adverse events (intent-to-treat).

RESULTS

Women made up 258/545 (47%) of the study population. More women than men were assigned to cohort A. Median follow-up was 72 weeks. Fewer women than men had HIV-1 RNA ≤200 copies/mL at week 48: 39% vs. 49% in cohort A and 83% vs. 89% in cohorts B, C, and D combined. More women experienced VF, grade ≥3 signs and symptoms, but similar grade ≥3 diagnoses or laboratory abnormalities.

CONCLUSIONS

More women than men entered the study with a resistance profile suggesting that their second-line regimen could have been effective in maintaining virologic suppression. The more frequent occurrence of grade ≥3 signs and symptoms in women suggests that tolerability issues were under recognized in women on protease inhibitor-based therapy.

摘要

背景

抗逆转录病毒(ART)药物暴露和治疗结果的性别差异研究支持这样一种假设,即某些 ART 组合在女性中可能不能很好地耐受。我们评估了在中低收入国家参与 ACTG A5288 的个体中,基于蛋白酶抑制剂的二线 ART 方案失败的个体的干预策略试验中,男性和女性之间结局的差异。

方法

根据耐药谱和 ART 史,将参与者分为 4 个队列(A-D)。队列 A 没有洛匹那韦/利托那韦(LPV/r)耐药,继续使用二线方案,而队列 B、C 和 D 的耐药性逐渐增加,并使用新型 ART 方案。在这项二次分析中,我们评估了主要终点(第 48 周时 HIV-1 RNA≤200 拷贝/ml)、确证病毒学失败(≥1000 拷贝/ml,VF)以及临床结局和不良事件(意向治疗)的性别差异。

结果

女性占研究人群的 258/545(47%)。与男性相比,更多的女性被分配到队列 A。中位随访时间为 72 周。第 48 周时,HIV-1 RNA≤200 拷贝/ml 的女性少于男性:队列 A 中分别为 39%和 49%,队列 B、C 和 D 中分别为 83%和 89%。更多的女性经历了 VF、≥3 级体征和症状,但相似的≥3 级诊断或实验室异常。

结论

与男性相比,更多的女性进入研究时的耐药谱表明,她们的二线方案可能有效地维持病毒学抑制。女性更频繁地出现≥3 级体征和症状表明,在基于蛋白酶抑制剂治疗的女性中,耐受性问题认识不足。