• 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

评估后期囊性纤维化五年预测生存率模型。

Evaluation of a five-year predicted survival model for cystic fibrosis in later time periods.

机构信息

Center for Quantitative Biology, University of Utah, Salt Lake City, Utah, USA.

The Adult Cystic Fibrosis Center at the University of Utah, Division of Respiratory, Critical Care and Occupational Pulmonary Medicine, Department of Internal Medicine, School of Medicine, University of Utah, Salt Lake City, Utah, USA.

出版信息

Sci Rep. 2020 Apr 20;10(1):6602. doi: 10.1038/s41598-020-63590-8.

DOI:10.1038/s41598-020-63590-8
PMID:32313191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7171119/
Abstract

We evaluated a multivariable logistic regression model predicting 5-year survival derived from a 1993-1997 cohort from the United States Cystic Fibrosis (CF) Foundation Patient Registry to assess whether therapies introduced since 1993 have altered applicability in cohorts, non-overlapping in time, from 1993-1998, 1999-2004, 2005-2010 and 2011-2016. We applied Kaplan-Meier statistics to assess unadjusted survival. We tested logistic regression model discrimination using the C-index and calibration using Hosmer-Lemeshow tests to examine original model performance and guide updating as needed. Kaplan-Meier age-adjusted 5-year probability of death in the CF population decreased substantially during 1993-2016. Patients in successive cohorts were generally healthier at entry, with higher average age, weight and lung function and fewer pulmonary exacerbations annually. CF-related diabetes prevalence, however, steadily increased. Newly derived multivariable logistic regression models for 5-year survival in new cohorts had similar estimated coefficients to the originals. The original model exhibited excellent calibration and discrimination when applied to later cohorts despite improved survival and remains useful for predicting 5-year survival. All models may be used to stratify patients for new studies, and the original coefficients may be useful as a baseline to search for additional but rare events that affect survival in CF.

摘要

我们评估了一个多变量逻辑回归模型,该模型预测了源自美国囊性纤维化 (CF) 基金会患者注册中心的 1993-1997 年队列的 5 年生存率,以评估自 1993 年以来引入的疗法是否改变了在时间上不重叠的 1993-1998 年、1999-2004 年、2005-2010 年和 2011-2016 年队列中的适用性。我们应用 Kaplan-Meier 统计来评估未经调整的生存率。我们使用 C 指数测试逻辑回归模型的判别能力,并使用 Hosmer-Lemeshow 检验进行校准,以检查原始模型的性能并根据需要进行更新。在 1993 年至 2016 年期间,CF 人群中未经调整的 5 年死亡率的 Kaplan-Meier 年龄调整后显著下降。连续队列中的患者在进入时通常更健康,平均年龄、体重和肺功能更高,每年的肺部恶化次数更少。然而,CF 相关糖尿病的患病率稳步上升。在新队列中,用于预测 5 年生存率的新多变量逻辑回归模型的估计系数与原始模型相似。尽管生存率有所提高,但原始模型在应用于后期队列时仍具有出色的校准和判别能力,仍然可用于预测 5 年生存率。所有模型都可用于对新研究进行分层,原始系数可作为基线,用于寻找影响 CF 患者生存的其他罕见事件。

相似文献

1
Evaluation of a five-year predicted survival model for cystic fibrosis in later time periods.评估后期囊性纤维化五年预测生存率模型。
Sci Rep. 2020 Apr 20;10(1):6602. doi: 10.1038/s41598-020-63590-8.
2
Up-to-date and projected estimates of survival for people with cystic fibrosis using baseline characteristics: A longitudinal study using UK patient registry data.使用基线特征对囊性纤维化患者进行最新和预计的生存估计:一项使用英国患者登记数据的纵向研究。
J Cyst Fibros. 2018 Mar;17(2):218-227. doi: 10.1016/j.jcf.2017.11.019. Epub 2018 Jan 6.
3
Case-mix adjustment for evaluation of mortality in cystic fibrosis.用于评估囊性纤维化死亡率的病例组合调整
Pediatr Pulmonol. 2002 Feb;33(2):99-105. doi: 10.1002/ppul.10042.
4
Disparities in Mortality of Hispanic Patients with Cystic Fibrosis in the United States. A National and Regional Cohort Study.美国 Hispanic 囊性纤维化患者死亡率的差异。一项全国性和区域性队列研究。
Am J Respir Crit Care Med. 2018 Oct 15;198(8):1055-1063. doi: 10.1164/rccm.201711-2357OC.
5
The effect of pregnancy on survival in women with cystic fibrosis.妊娠对囊性纤维化女性患者生存的影响。
Chest. 2003 Oct;124(4):1460-8. doi: 10.1378/chest.124.4.1460.
6
Heterogeneity in Survival in Adult Patients With Cystic Fibrosis With FEV < 30% of Predicted in the United States.美国预测FEV<30%的成年囊性纤维化患者生存的异质性
Chest. 2017 Jun;151(6):1320-1328. doi: 10.1016/j.chest.2017.01.019. Epub 2017 Jan 20.
7
Influence of diabetes on survival in patients with cystic fibrosis before and after lung transplantation.糖尿病对肺移植前后囊性纤维化患者生存的影响。
J Thorac Cardiovasc Surg. 2015 Sep;150(3):707-13.e2. doi: 10.1016/j.jtcvs.2015.06.041. Epub 2015 Jun 26.
8
Validation and use of a parametric model for projecting cystic fibrosis survivorship beyond observed data: a birth cohort analysis.验证和使用参数模型来预测囊性纤维化患者的生存情况,超越观察数据:一项出生队列分析。
Thorax. 2011 Aug;66(8):674-9. doi: 10.1136/thoraxjnl-2011-200038. Epub 2011 Jun 8.
9
Gender differences in outcomes of patients with cystic fibrosis.囊性纤维化患者预后的性别差异。
J Womens Health (Larchmt). 2014 Dec;23(12):1012-20. doi: 10.1089/jwh.2014.4985.
10
Longevity of patients with cystic fibrosis in 2000 to 2010 and beyond: survival analysis of the Cystic Fibrosis Foundation patient registry.2000年至2010年及以后囊性纤维化患者的寿命:囊性纤维化基金会患者登记处的生存分析
Ann Intern Med. 2014 Aug 19;161(4):233-41. doi: 10.7326/M13-0636.

引用本文的文献

1
Impact of CFTR Modulators on Longitudinal Cystic Fibrosis Survival and Mortality: Review and Secondary Analysis.CFTR调节剂对囊性纤维化患者长期生存及死亡率的影响:综述与二次分析
Pulm Ther. 2025 Jul 11. doi: 10.1007/s41030-025-00303-4.
2
Is Obesity a Problem in New Cystic Fibrosis Treatments?肥胖症是否成为新的囊性纤维化治疗方法的问题?
Nutrients. 2024 Sep 14;16(18):3103. doi: 10.3390/nu16183103.
3
Predicting weight gain in patients with cystic fibrosis on triple combination modulator.预测接受三联组合调节剂治疗的囊性纤维化患者的体重增加。

本文引用的文献

1
Modeling long-term health outcomes of patients with cystic fibrosis homozygous for F508del-CFTR treated with lumacaftor/ivacaftor.模拟 F508del-CFTR 纯合子囊性纤维化患者接受 lumacaftor/ivacaftor 治疗的长期健康结局。
Ther Adv Respir Dis. 2019 Jan-Dec;13:1753466618820186. doi: 10.1177/1753466618820186.
2
ECFS best practice guidelines: the 2018 revision.欧洲过敏与临床免疫学会变应原标准:2018 修订版。
J Cyst Fibros. 2018 Mar;17(2):153-178. doi: 10.1016/j.jcf.2018.02.006. Epub 2018 Mar 3.
3
A guide to interpreting estimated median age of survival in cystic fibrosis patient registry reports.
Pediatr Pulmonol. 2024 Jun;59(6):1724-1730. doi: 10.1002/ppul.26982. Epub 2024 Apr 12.
4
Airway inflammation accelerates pulmonary exacerbations in cystic fibrosis.气道炎症会加速囊性纤维化患者的肺部病情恶化。
iScience. 2024 Jan 9;27(3):108835. doi: 10.1016/j.isci.2024.108835. eCollection 2024 Mar 15.
5
Using temporal recalibration to improve the calibration of risk prediction models in competing risk settings when there are trends in survival over time.利用时变校准来改进风险预测模型在竞争风险环境中的校准,当存在随时间变化的生存趋势时。
Stat Med. 2023 Nov 30;42(27):5007-5024. doi: 10.1002/sim.9898. Epub 2023 Sep 13.
6
Calibration and validation of modeled 5-year survival predictions among people with cystic fibrosis treated with the cystic fibrosis transmembrane conductance regulator modulator ivacaftor using United States registry data.使用美国登记数据对囊性纤维化跨膜电导调节剂调节剂 ivacaftor 治疗的囊性纤维化患者的 5 年生存预测模型进行校准和验证。
PLoS One. 2023 Apr 12;18(4):e0283479. doi: 10.1371/journal.pone.0283479. eCollection 2023.
7
Lung Function Decline in Cystic Fibrosis: Impact of Data Availability and Modeling Strategies on Clinical Interpretations.肺功能在囊性纤维化中的下降:数据可用性和建模策略对临床解释的影响。
Ann Am Thorac Soc. 2023 Jul;20(7):958-968. doi: 10.1513/AnnalsATS.202209-829OC.
8
Surgical considerations in cystic fibrosis: what every general surgeon needs to know.囊性纤维化的外科考虑因素:普通外科医生需要了解的知识。
ANZ J Surg. 2022 Oct;92(10):2425-2432. doi: 10.1111/ans.17948. Epub 2022 Aug 3.
9
Ultrasound-Derived Diaphragm Contractile Reserve as a Marker of Clinical Status in Patients With Cystic Fibrosis.超声测量的膈肌收缩储备作为囊性纤维化患者临床状态的标志物
Front Physiol. 2022 Jan 10;12:808770. doi: 10.3389/fphys.2021.808770. eCollection 2021.
10
New Insights in Microbial Species Predicting Lung Function Decline in CF: Lessons from the MucoFong Project.微生物物种预测囊性纤维化肺功能下降的新见解:来自黏液真菌项目的经验教训。
J Clin Med. 2021 Aug 21;10(16):3725. doi: 10.3390/jcm10163725.
解读囊性纤维化患者注册报告中估计生存中位数的指南。
J Cyst Fibros. 2018 Mar;17(2):213-217. doi: 10.1016/j.jcf.2017.11.014. Epub 2018 Feb 2.
4
Up-to-date and projected estimates of survival for people with cystic fibrosis using baseline characteristics: A longitudinal study using UK patient registry data.使用基线特征对囊性纤维化患者进行最新和预计的生存估计:一项使用英国患者登记数据的纵向研究。
J Cyst Fibros. 2018 Mar;17(2):218-227. doi: 10.1016/j.jcf.2017.11.019. Epub 2018 Jan 6.
5
Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del.Tezacaftor-Ivacaftor 治疗纯合子 Phe508del 突变型囊性纤维化患者的疗效
N Engl J Med. 2017 Nov 23;377(21):2013-2023. doi: 10.1056/NEJMoa1709846. Epub 2017 Nov 3.
6
Survival Comparison of Patients With Cystic Fibrosis in Canada and the United States: A Population-Based Cohort Study.加拿大和美国囊性纤维化患者的生存比较:一项基于人群的队列研究。
Ann Intern Med. 2017 Apr 18;166(8):537-546. doi: 10.7326/M16-0858. Epub 2017 Mar 14.
7
The Dynamics of Disease Progression in Cystic Fibrosis.囊性纤维化疾病进展的动态变化
PLoS One. 2016 Jun 1;11(6):e0156752. doi: 10.1371/journal.pone.0156752. eCollection 2016.
8
Improving performance in the detection and management of cystic fibrosis-related diabetes in the Mountain West Cystic Fibrosis Consortium.提高 Mountain West Cystic Fibrosis Consortium 在囊性纤维化相关性糖尿病的检测和管理方面的表现。
BMJ Open Diabetes Res Care. 2016 Apr 29;4(1):e000183. doi: 10.1136/bmjdrc-2015-000183. eCollection 2016.
9
The Cystic Fibrosis Foundation Patient Registry. Design and Methods of a National Observational Disease Registry.囊性纤维化基金会患者登记处。一个国家观察性疾病登记处的设计与方法。
Ann Am Thorac Soc. 2016 Jul;13(7):1173-9. doi: 10.1513/AnnalsATS.201511-781OC.
10
Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.尽管胰岛细胞数量未减少,但囊性纤维化猪的血糖调节和胰岛素分泌仍存在异常。
Clin Sci (Lond). 2015 Jan;128(2):131-42. doi: 10.1042/CS20140059.