• 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

常染色体显性多囊肾病患者开始透析前后肾脏和肝脏体积的变化

Changes in Kidney and Liver Volumes in Patients With Autosomal Dominant Polycystic Kidney Disease Before and After Dialysis Initiation.

作者信息

Suwabe Tatsuya, Ubara Yoshifumi, Oba Yuki, Mizuno Hiroki, Ikuma Daisuke, Yamanouchi Masayuki, Sekine Akinari, Tanaka Kiho, Hasegawa Eiko, Hoshino Junichi, Sawa Naoki

机构信息

Department of Nephrology, Toranomon Hospital, Tokyo and Kawasaki, Japan.

Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.

出版信息

Mayo Clin Proc Innov Qual Outcomes. 2023 Jan 20;7(1):69-80. doi: 10.1016/j.mayocpiqo.2022.12.005. eCollection 2023 Feb.

DOI:10.1016/j.mayocpiqo.2022.12.005
PMID:36712823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9873948/
Abstract

OBJECTIVE

To examine the changes in total kidney volume (TKV) and total liver volume (TLV) before and after dialysis initiation in patients with autosomal dominant polycystic kidney disease.

PATIENTS AND METHODS

This was a retrospective, single-center cohort study to investigate the changes in TKV and TLV before and after dialysis initiation, along with influencing factors, using linear mixed models. We enrolled 95 patients with autosomal dominant polycystic kidney disease (85 receiving hemodialysis [HD] and 10 receiving peritoneal dialysis [PD]) who began receiving dialysis at Toranomon Hospital from January 1, 2008, to December 31, 2020.

RESULTS

The least squares mean TKV ratio (TKV at each time point/TKV at dialysis initiation) was 63.8% (95% confidence interval [CI], 54.7%-72.9%) at 6 years before dialysis initiation and 95.5% (95% CI, 82.9%-108.2%) at 6 years after dialysis initiation (<.001). A multivariate linear mixed model analysis revealed that dialysis style (HD or PD) had the strongest effect on changes in TKV (=.002). The least squares mean TLV ratio was 98.2% (95% CI, 88.4%-108.0%) at 6 years before dialysis initiation and 95.7% (95% CI, 85.2%-106.2%) at 6 years after dialysis initiation (=.01). Although PD did not have significant effects on changes in TLV (=.27), the changes in TLV were greater in patients on PD than in those on HD.

CONCLUSION

The TKV increased until dialysis initiation and generally decreased after dialysis initiation. The TLV continued to increase even after dialysis initiation, however, changes in the TLV significantly decreased after dialysis initiation. The increases in TKV and TLV were greater in patients on PD than in those on HD.

摘要

目的

研究常染色体显性遗传性多囊肾病患者开始透析前后的总肾体积(TKV)和总肝体积(TLV)变化。

患者与方法

这是一项回顾性单中心队列研究,采用线性混合模型调查开始透析前后TKV和TLV的变化及其影响因素。我们纳入了95例常染色体显性遗传性多囊肾病患者(85例接受血液透析[HD],10例接受腹膜透析[PD]),这些患者于2008年1月1日至2020年12月31日在东京新桥医院开始接受透析治疗。

结果

透析开始前6年,TKV比值(各时间点的TKV/透析开始时的TKV)的最小二乘均值为63.8%(95%置信区间[CI],54.7%-72.9%),透析开始后6年为95.5%(95%CI,82.9%-108.2%)(P<0.001)。多变量线性混合模型分析显示,透析方式(HD或PD)对TKV变化的影响最大(P=0.002)。透析开始前6年,TLV比值的最小二乘均值为98.2%(95%CI,88.4%-108.0%),透析开始后6年为95.7%(95%CI,85.2%-106.2%)(P=0.01)。虽然PD对TLV变化无显著影响(P=0.27),但接受PD治疗的患者TLV变化大于接受HD治疗的患者。

结论

TKV在透析开始前增加,透析开始后总体下降。TLV在透析开始后仍继续增加,不过透析开始后TLV的变化显著减小。接受PD治疗的患者TKV和TLV的增加幅度大于接受HD治疗的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/4ca14b7f733a/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/595bed2d4d67/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/dbb573a34898/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/4ca14b7f733a/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/595bed2d4d67/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/dbb573a34898/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec9/9873948/4ca14b7f733a/gr3.jpg

相似文献

1
Changes in Kidney and Liver Volumes in Patients With Autosomal Dominant Polycystic Kidney Disease Before and After Dialysis Initiation.常染色体显性多囊肾病患者开始透析前后肾脏和肝脏体积的变化
Mayo Clin Proc Innov Qual Outcomes. 2023 Jan 20;7(1):69-80. doi: 10.1016/j.mayocpiqo.2022.12.005. eCollection 2023 Feb.
2
Automatic Measurement of Kidney and Liver Volumes from MR Images of Patients Affected by Autosomal Dominant Polycystic Kidney Disease.应用于常染色体显性多囊肾病患者磁共振图像的肾脏和肝脏自动容积测量。
J Am Soc Nephrol. 2019 Aug;30(8):1514-1522. doi: 10.1681/ASN.2018090902. Epub 2019 Jul 3.
3
Volume regression of native polycystic kidneys after renal transplantation.肾移植后天然多囊肾的体积缩小
Nephrol Dial Transplant. 2016 Jan;31(1):73-9. doi: 10.1093/ndt/gfv227. Epub 2015 Jun 4.
4
Acute renal intracystic hemorrhage in patients with autosomal dominant polycystic kidney disease.常染色体显性多囊肾病患者的急性肾内囊内出血。
J Nephrol. 2023 May;36(4):999-1010. doi: 10.1007/s40620-022-01562-z. Epub 2023 Feb 8.
5
Safety study of somatostatin analogue octreotide for autosomal dominant polycystic kidney disease in Japan.日本生长抑素类似物奥曲肽用于常染色体显性多囊肾病的安全性研究。
Clin Exp Nephrol. 2015 Aug;19(4):746-52. doi: 10.1007/s10157-014-1047-1. Epub 2014 Oct 29.
6
Long-acting somatostatin analogue treatments in autosomal dominant polycystic kidney disease and polycystic liver disease: a systematic review and meta-analysis.常效生长抑素类似物治疗常染色体显性遗传多囊肾病和多囊肝病:系统评价和荟萃分析。
BMJ Open. 2020 Jan 9;10(1):e032620. doi: 10.1136/bmjopen-2019-032620.
7
Hemorrhagic Cysts and Other MR Biomarkers for Predicting Renal Dysfunction Progression in Autosomal Dominant Polycystic Kidney Disease.出血性囊肿及其他磁共振生物标志物在预测常染色体显性多囊肾病肾功能不全进展中的作用
J Magn Reson Imaging. 2021 Feb;53(2):564-576. doi: 10.1002/jmri.27360. Epub 2020 Sep 23.
8
Factors predicting decline in renal function and kidney volume growth in autosomal dominant polycystic kidney disease: a prospective cohort study (Japanese Polycystic Kidney Disease registry: J-PKD).常染色体显性多囊肾病中肾功能下降和肾体积增长的预测因素:一项前瞻性队列研究(日本多囊肾病登记处:J-PKD)
Clin Exp Nephrol. 2021 Sep;25(9):970-980. doi: 10.1007/s10157-021-02068-x. Epub 2021 Apr 29.
9
End-Stage Kidney Disease in Patients With Autosomal Dominant Polycystic Kidney Disease: A 12-Year Study Based on the Canadian Organ Replacement Registry.常染色体显性多囊肾病患者的终末期肾病:一项基于加拿大器官替代登记处的12年研究
Can J Kidney Health Dis. 2018 Jun 11;5:2054358118778568. doi: 10.1177/2054358118778568. eCollection 2018.
10
RESET-PKD: a pilot trial on short-term ketogenic interventions in autosomal dominant polycystic kidney disease.RESET-PKD 研究:常染色体显性遗传多囊肾病中短期生酮干预的初步试验
Nephrol Dial Transplant. 2023 Jun 30;38(7):1623-1635. doi: 10.1093/ndt/gfac311.

引用本文的文献

1
Brachial-ankle pulse wave velocity predicts liver volume in patients with autosomal dominant polycystic kidney disease.肱踝脉搏波速度可预测常染色体显性多囊肾病患者的肝脏体积。
PLoS One. 2025 Jul 21;20(7):e0328133. doi: 10.1371/journal.pone.0328133. eCollection 2025.
2
Nephrectomy in autosomal dominant polycystic kidney disease: a consensus statement of the ERA Genes & Kidney Working Group.常染色体显性多囊肾病的肾切除术:欧洲肾脏协会基因与肾脏工作组的共识声明
Nephrol Dial Transplant. 2025 Apr 28;40(5):1032-1054. doi: 10.1093/ndt/gfaf019.

本文引用的文献

1
Fluid Overload.液体过载
Front Vet Sci. 2021 Jun 29;8:668688. doi: 10.3389/fvets.2021.668688. eCollection 2021.
2
Autosomal Dominant Polycystic Kidney Disease in which the Polycystic Liver Volume Was Reduced by Rigorous Blood Pressure Control.常染色体显性遗传性多囊肾病患者,通过严格的血压控制降低多囊肝体积。
Intern Med. 2022 Jan 1;61(1):49-52. doi: 10.2169/internalmedicine.7441-21. Epub 2021 Jul 3.
3
Autosomal dominant polycystic kidney disease.常染色体显性遗传性多囊肾病。
Lancet. 2019 Mar 2;393(10174):919-935. doi: 10.1016/S0140-6736(18)32782-X. Epub 2019 Feb 25.
4
Use of a micro-balloon catheter in transcatheter arterial embolization of the renal artery for recurrence of symptoms of autosomal dominant polycystic kidney disease.微球囊导管在经导管动脉栓塞肾动脉治疗常染色体显性多囊肾病症状复发中的应用。
Acta Radiol Open. 2018 Dec 10;7(12):2058460118818849. doi: 10.1177/2058460118818849. eCollection 2018 Dec.
5
Suitability of Patients with Autosomal Dominant Polycystic Kidney Disease for Renal Transcatheter Arterial Embolization.常染色体显性遗传性多囊肾病患者接受肾动脉导管栓塞术的适用性
J Am Soc Nephrol. 2016 Jul;27(7):2177-87. doi: 10.1681/ASN.2015010067. Epub 2015 Nov 30.
6
The PROPKD Score: A New Algorithm to Predict Renal Survival in Autosomal Dominant Polycystic Kidney Disease.PROPKD评分:一种预测常染色体显性多囊肾病肾脏存活情况的新算法。
J Am Soc Nephrol. 2016 Mar;27(3):942-51. doi: 10.1681/ASN.2015010016. Epub 2015 Jul 6.
7
Autosomal dominant polycystic kidney disease: the changing face of clinical management.常染色体显性遗传性多囊肾病:临床管理的变化。
Lancet. 2015 May 16;385(9981):1993-2002. doi: 10.1016/S0140-6736(15)60907-2.
8
Volume regression of native polycystic kidneys after renal transplantation.肾移植后天然多囊肾的体积缩小
Nephrol Dial Transplant. 2016 Jan;31(1):73-9. doi: 10.1093/ndt/gfv227. Epub 2015 Jun 4.
9
Evaluation of fluid status related parameters in hemodialysis and peritoneal dialysis patients: Clinical usefulness of bioimpedance analysis.血液透析和腹膜透析患者液体状态相关参数的评估:生物电阻抗分析的临床应用价值
Medicina (Kaunas). 2014;50(5):269-74. doi: 10.1016/j.medici.2014.10.007. Epub 2014 Nov 1.
10
Imaging classification of autosomal dominant polycystic kidney disease: a simple model for selecting patients for clinical trials.常染色体显性遗传多囊肾病的影像学分类:一种用于选择临床试验患者的简单模型。
J Am Soc Nephrol. 2015 Jan;26(1):160-72. doi: 10.1681/ASN.2013101138. Epub 2014 Jun 5.