IgD型全身性轻链淀粉样变性患者临床特点分析

Q3 Medicine
G X Duan, L Wen, N Peng, Y Liu, X L Dou, X L Sun, J Lu
{"title":"IgD型全身性轻链淀粉样变性患者临床特点分析","authors":"G X Duan, L Wen, N Peng, Y Liu, X L Dou, X L Sun, J Lu","doi":"10.3760/cma.j.cn112137-20250218-00384","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To analyze the clinical characteristics of patients with IgD type systemic light chain (AL) amyloidosis. <b>Methods:</b> The patients diagnosed with IgD-type AL amyloidosis at Peking University People's Hospital and the First Affiliated Hospital of Dalian Medical University from June 2013 to April 2023 (IgD group) were retrospectively included. These patients were matched with non-IgD type AL amyloidosis patients using a 1∶4 propensity score (non-IgD group). The general clinical data of the patients (age, gender, the type of light chain, results of relevant examinations and so on), treatment planss, and efficacy were collected (the corresponding sample size was reduced due to the fact that some patients did not undergo relevant examinations or lost testing data). Follow-up was conducted until August 2024 to compare the clinical characteristics of the both groups of patients. <b>Results:</b> A total of 45 patients were included in the study. The IgD group was comprised of 9 patients, with 6 males and 3 females, and an average age of (58±12) years. The non-IgD group consisted of 36 patients, including 24 males and 12 females, with an average age of (58±10) years. The overall median follow-up time [<i>M</i> (<i>Q</i><sub>1</sub>, <i>Q</i><sub>3</sub>)]was 58 (31, 84) months. In the IgD group, one patient had Kappa type while the remaining were Lambda type; seven cases involved kidney, and 6 cases involved heart. Two patients in IgD group had p53 deletion, but there was no p53 deletion in non-IgD group. The rate of soft tissue involvement [55.6% (5/9) vs 13.9% (5/36), <i>P</i>=0.025] and the level of free light chain difference (dFLC) (2 424 vs 140 mg/L, <i>P</i>=0.002) in the IgD group were higher than those in the non IgD group. Hemoglobin levels were lower in the IgD group [(102.3±24.0) vs (128.4±22.1) g/L, <i>P</i>=0.003], as well as lactate dehydrogenase [(190.1±26.0) vs (236.1±62.8) U/L, <i>P</i>=0.002]. A total of 8 patients in the IgD group received first-line treatment, among which 7 achieved hematological remission. Three patients in the IgD group and 5 patients in the non-IgD group died. <b>Conclusions:</b> The incidence rate for soft tissue involvement and dFLC level of the patients with IgD-type AL amyloidosis are higher in the IgD group. Conversely, hemoglobin levels and lactate dehydrogenase are lower.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 33","pages":"2852-2858"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Clinical characteristics analysis of patients with IgD type systemic light chain amyloidosis].\",\"authors\":\"G X Duan, L Wen, N Peng, Y Liu, X L Dou, X L Sun, J Lu\",\"doi\":\"10.3760/cma.j.cn112137-20250218-00384\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Objective:</b> To analyze the clinical characteristics of patients with IgD type systemic light chain (AL) amyloidosis. <b>Methods:</b> The patients diagnosed with IgD-type AL amyloidosis at Peking University People's Hospital and the First Affiliated Hospital of Dalian Medical University from June 2013 to April 2023 (IgD group) were retrospectively included. These patients were matched with non-IgD type AL amyloidosis patients using a 1∶4 propensity score (non-IgD group). The general clinical data of the patients (age, gender, the type of light chain, results of relevant examinations and so on), treatment planss, and efficacy were collected (the corresponding sample size was reduced due to the fact that some patients did not undergo relevant examinations or lost testing data). Follow-up was conducted until August 2024 to compare the clinical characteristics of the both groups of patients. <b>Results:</b> A total of 45 patients were included in the study. The IgD group was comprised of 9 patients, with 6 males and 3 females, and an average age of (58±12) years. The non-IgD group consisted of 36 patients, including 24 males and 12 females, with an average age of (58±10) years. The overall median follow-up time [<i>M</i> (<i>Q</i><sub>1</sub>, <i>Q</i><sub>3</sub>)]was 58 (31, 84) months. In the IgD group, one patient had Kappa type while the remaining were Lambda type; seven cases involved kidney, and 6 cases involved heart. Two patients in IgD group had p53 deletion, but there was no p53 deletion in non-IgD group. The rate of soft tissue involvement [55.6% (5/9) vs 13.9% (5/36), <i>P</i>=0.025] and the level of free light chain difference (dFLC) (2 424 vs 140 mg/L, <i>P</i>=0.002) in the IgD group were higher than those in the non IgD group. Hemoglobin levels were lower in the IgD group [(102.3±24.0) vs (128.4±22.1) g/L, <i>P</i>=0.003], as well as lactate dehydrogenase [(190.1±26.0) vs (236.1±62.8) U/L, <i>P</i>=0.002]. A total of 8 patients in the IgD group received first-line treatment, among which 7 achieved hematological remission. Three patients in the IgD group and 5 patients in the non-IgD group died. <b>Conclusions:</b> The incidence rate for soft tissue involvement and dFLC level of the patients with IgD-type AL amyloidosis are higher in the IgD group. Conversely, hemoglobin levels and lactate dehydrogenase are lower.</p>\",\"PeriodicalId\":24023,\"journal\":{\"name\":\"Zhonghua yi xue za zhi\",\"volume\":\"105 33\",\"pages\":\"2852-2858\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhonghua yi xue za zhi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3760/cma.j.cn112137-20250218-00384\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhonghua yi xue za zhi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/cma.j.cn112137-20250218-00384","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

目的:分析IgD型系统性轻链(AL)淀粉样变的临床特点。方法:回顾性分析2013年6月至2023年4月北京大学人民医院和大连医科大学第一附属医院诊断为IgD型AL淀粉样变的患者(IgD组)。采用1∶4倾向性评分(非igd组)与非igd型AL淀粉样变性患者进行配对。收集患者的一般临床资料(年龄、性别、轻链类型、相关检查结果等)、治疗方案、疗效(因部分患者未进行相关检查或检测资料丢失,减少相应样本量)。随访至2024年8月,比较两组患者的临床特征。结果:共纳入45例患者。IgD组9例,男6例,女3例,平均年龄(58±12)岁。非igd组36例,其中男性24例,女性12例,平均年龄(58±10)岁。总体中位随访时间[M (Q1, Q3)]为58(31,84)个月。IgD组1例为Kappa型,其余为Lambda型;7例累及肾脏,6例累及心脏。IgD组有2例p53缺失,非IgD组无p53缺失。IgD组软组织受累率(55.6% (5/9)vs 13.9% (5/36), P=0.025)和游离轻链差(dFLC)水平(2 424 vs 140 mg/L, P=0.002)高于非IgD组。IgD组血红蛋白水平较低[(102.3±24.0)vs(128.4±22.1)g/L, P=0.003],乳酸脱氢酶水平较低[(190.1±26.0)vs(236.1±62.8)U/L, P=0.002]。IgD组共有8例患者接受一线治疗,其中7例患者血液学缓解。IgD组3例死亡,非IgD组5例死亡。结论:IgD组AL淀粉样变患者的软组织受累发生率及dFLC水平均高于IgD组。相反,血红蛋白水平和乳酸脱氢酶较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical characteristics analysis of patients with IgD type systemic light chain amyloidosis].

Objective: To analyze the clinical characteristics of patients with IgD type systemic light chain (AL) amyloidosis. Methods: The patients diagnosed with IgD-type AL amyloidosis at Peking University People's Hospital and the First Affiliated Hospital of Dalian Medical University from June 2013 to April 2023 (IgD group) were retrospectively included. These patients were matched with non-IgD type AL amyloidosis patients using a 1∶4 propensity score (non-IgD group). The general clinical data of the patients (age, gender, the type of light chain, results of relevant examinations and so on), treatment planss, and efficacy were collected (the corresponding sample size was reduced due to the fact that some patients did not undergo relevant examinations or lost testing data). Follow-up was conducted until August 2024 to compare the clinical characteristics of the both groups of patients. Results: A total of 45 patients were included in the study. The IgD group was comprised of 9 patients, with 6 males and 3 females, and an average age of (58±12) years. The non-IgD group consisted of 36 patients, including 24 males and 12 females, with an average age of (58±10) years. The overall median follow-up time [M (Q1, Q3)]was 58 (31, 84) months. In the IgD group, one patient had Kappa type while the remaining were Lambda type; seven cases involved kidney, and 6 cases involved heart. Two patients in IgD group had p53 deletion, but there was no p53 deletion in non-IgD group. The rate of soft tissue involvement [55.6% (5/9) vs 13.9% (5/36), P=0.025] and the level of free light chain difference (dFLC) (2 424 vs 140 mg/L, P=0.002) in the IgD group were higher than those in the non IgD group. Hemoglobin levels were lower in the IgD group [(102.3±24.0) vs (128.4±22.1) g/L, P=0.003], as well as lactate dehydrogenase [(190.1±26.0) vs (236.1±62.8) U/L, P=0.002]. A total of 8 patients in the IgD group received first-line treatment, among which 7 achieved hematological remission. Three patients in the IgD group and 5 patients in the non-IgD group died. Conclusions: The incidence rate for soft tissue involvement and dFLC level of the patients with IgD-type AL amyloidosis are higher in the IgD group. Conversely, hemoglobin levels and lactate dehydrogenase are lower.

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
Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
400
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信