• 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

难治性乳糜泻和肠病相关T细胞淋巴瘤患者在诊断时表现出严重营养不良和吸收不良。

Refractory celiac disease and EATL patients show severe malnutrition and malabsorption at diagnosis.

作者信息

Wierdsma Nicolette J, Nijeboer Petula, de van der Schueren Marian A E, Berkenpas Marijke, van Bodegraven Ad A, Mulder Chris J J

机构信息

Department of Nutrition and Dietetics, VU University Medical Centre, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.

Department of Gastroenterology, Celiac Centre Amsterdam, VU University Medical Centre, Amsterdam, The Netherlands.

出版信息

Clin Nutr. 2016 Jun;35(3):685-91. doi: 10.1016/j.clnu.2015.04.014. Epub 2015 Apr 30.

DOI:10.1016/j.clnu.2015.04.014
PMID:25979847
Abstract

BACKGROUND & AIMS: Refractory celiac disease type II (RCDII) and EATL (Enteropathy Associated T-cell Lymphoma) are (pre)malignant complications of celiac disease (CD). Data on malnutrition and intestinal absorption is lacking in these patients. Therefore, the aim of the study is to comprehensively assess nutritional status and intestinal absorption capacity of patients with RCDII and EATL, compared with data of newly diagnosed CD patients.

METHODS

Observational study in tertiary care setting in RCDII (n = 24, 63.8 ± 8.2 y), EATL (n = 25, 62.3 ± 5.7 y) and CD patients (n = 43, 45.6 ± 14.8 y). At diagnosis, anthropometry (BMI, unintentional weight loss, fat-free mass index (FFMI), handgrip strength (HGS), nutritional intake, fecal losses and Resting Energy Expenditure (REE)) were assessed.

RESULTS

Low BMI (<18.5) was more often observed in RCDII patients than in CD or EATL patients (in 33%, 12% and 12%, respectively, p = 0.029). EATL patients more frequently had unintentional weight loss (>10%) than CD or RCDII patients (in 58%, 19% and 39% of patients, respectively; p = 0.005/0.082). Energy malabsorption (<85%) was detected in 44% and 33% of RCDII and EATL patients, vs 21.6% in CD (NS). Fecal energy losses were higher in RCDII than in CD patients (589 ± 451 vs 277 ± 137 kcal/d, p = 0.017). REE was underestimated by predicted-REE with>10% in 60% of RCDII, 89% of EATL, and 38% of CD patients (p = 0.006). Low FFMI and HGS were detected in one third and two thirds of all patients, respectively.

CONCLUSIONS

The nutritional status of patients with RCDII and EATL is inferior compared with untreated naïve CD patients at presentation. Both malabsorption as well as hypermetabolism contribute to malnutrition.

摘要

背景与目的

II型难治性乳糜泻(RCDII)和肠病相关T细胞淋巴瘤(EATL)是乳糜泻(CD)的(前)恶性并发症。这些患者缺乏营养不良和肠道吸收方面的数据。因此,本研究的目的是全面评估RCDII和EATL患者的营养状况和肠道吸收能力,并与新诊断的CD患者的数据进行比较。

方法

在三级医疗机构对RCDII患者(n = 24,63.8±8.2岁)、EATL患者(n = 25,62.3±5.7岁)和CD患者(n = 43,45.6±14.8岁)进行观察性研究。在诊断时,评估人体测量指标(体重指数、非故意体重减轻、去脂体重指数(FFMI)、握力(HGS))、营养摄入、粪便损失和静息能量消耗(REE)。

结果

RCDII患者中低体重指数(<18.5)的发生率高于CD或EATL患者(分别为33%、12%和12%,p = 0.029)。EATL患者非故意体重减轻(>10%)的发生率高于CD或RCDII患者(分别为58%、19%和39%的患者;p = 0.005/0.082)。44%的RCDII患者和33%的EATL患者存在能量吸收不良(<85%),而CD患者中这一比例为21.6%(无统计学差异)。RCDII患者的粪便能量损失高于CD患者(589±451 vs 277±137千卡/天,p = 0.017)。60%的RCDII患者、89%的EATL患者和38%的CD患者的静息能量消耗被预测静息能量消耗低估>10%(p = 0.006)。所有患者中分别有三分之一和三分之二检测到低去脂体重指数和低握力。

结论

与初诊时未经治疗的单纯CD患者相比,RCDII和EATL患者的营养状况较差。吸收不良和高代谢均导致营养不良。

相似文献

1
Refractory celiac disease and EATL patients show severe malnutrition and malabsorption at diagnosis.难治性乳糜泻和肠病相关T细胞淋巴瘤患者在诊断时表现出严重营养不良和吸收不良。
Clin Nutr. 2016 Jun;35(3):685-91. doi: 10.1016/j.clnu.2015.04.014. Epub 2015 Apr 30.
2
Oncogenetic landscape of lymphomagenesis in coeliac disease.腹腔疾病相关淋巴瘤发病的oncogenetic 图谱。
Gut. 2022 Mar;71(3):497-508. doi: 10.1136/gutjnl-2020-322935. Epub 2021 Feb 12.
3
Complications of coeliac disease.乳糜泻的并发症。
Best Pract Res Clin Gastroenterol. 2015 Jun;29(3):451-8. doi: 10.1016/j.bpg.2015.05.005. Epub 2015 May 14.
4
Enteropathy-Associated T cell Lymphoma.肠病相关 T 细胞淋巴瘤。
Curr Hematol Malig Rep. 2021 Apr;16(2):140-147. doi: 10.1007/s11899-021-00634-4. Epub 2021 May 19.
5
Malabsorption is a major contributor to underweight in Crohn's disease patients in remission.吸收不良是缓解期克罗恩病患者体重过轻的主要原因。
Nutrition. 2006 Sep;22(9):855-9. doi: 10.1016/j.nut.2006.05.013.
6
NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: a CELAC study.NKp46 是一种诊断生物标志物,可能是胃肠道 T 细胞淋巴增生性疾病的治疗靶点:CELAC 研究。
Gut. 2019 Aug;68(8):1396-1405. doi: 10.1136/gutjnl-2018-317371. Epub 2018 Nov 17.
7
Enteropathy associated T-cell lymphoma and its precursor lesions.肠病相关 T 细胞淋巴瘤及其前驱病变。
Best Pract Res Clin Gastroenterol. 2010 Feb;24(1):43-56. doi: 10.1016/j.bpg.2009.11.002.
8
[Acute intestinal obstruction revealing enteropathy associated t-cell lymphoma, about a case].[急性肠梗阻揭示肠病相关T细胞淋巴瘤,一例报告]
Pan Afr Med J. 2016 Feb 19;23:48. doi: 10.11604/pamj.2016.23.48.8909. eCollection 2016.
9
Surgery in (pre)malignant celiac disease.(前)恶性腹腔疾病的外科手术
World J Gastroenterol. 2015 Nov 21;21(43):12403-9. doi: 10.3748/wjg.v21.i43.12403.
10
Type II enteropathy-associated T-cell lymphoma: a distinct aggressive lymphoma with frequent γδ T-cell receptor expression.Ⅱ型肠病相关 T 细胞淋巴瘤:一种具有显著侵袭性的淋巴瘤,常表达γδ T 细胞受体。
Am J Surg Pathol. 2011 Oct;35(10):1557-69. doi: 10.1097/PAS.0b013e318222dfcd.

引用本文的文献

1
Malignancies in Celiac Disease-A Hidden Threat with Diagnostic Pitfalls.乳糜泻相关恶性肿瘤——存在诊断陷阱的隐匿威胁
Biomedicines. 2025 Jun 19;13(6):1507. doi: 10.3390/biomedicines13061507.
2
Enteropathy-Associated T-Cell Lymphoma Treated With Autologous Hematopoietic Stem-Cell Transplant: A Glimmer of Hope?自体造血干细胞移植治疗肠病相关T细胞淋巴瘤:一线希望?
ACG Case Rep J. 2024 Oct 10;11(10):e01529. doi: 10.14309/crj.0000000000001529. eCollection 2024 Oct.
3
Refractory celiac disease and its mimickers: a review on pathogenesis, clinical-pathological features and therapeutic challenges.
难治性乳糜泻及其模仿者:关于发病机制、临床病理特征和治疗挑战的综述
Front Oncol. 2023 Nov 7;13:1273305. doi: 10.3389/fonc.2023.1273305. eCollection 2023.
4
Follow-Up of Celiac Disease in Adults: "When, What, Who, and Where".成人乳糜泻的随访:“何时、何事、何人以及何地”。
Nutrients. 2023 Apr 24;15(9):2048. doi: 10.3390/nu15092048.
5
The Dietary and Non-Dietary Management of Osteoporosis in Adult-Onset Celiac Disease: Current Status and Practical Guidance.成人发病乳糜泻中骨质疏松症的饮食和非饮食管理:现状和实用指南。
Nutrients. 2022 Oct 28;14(21):4554. doi: 10.3390/nu14214554.
6
Artificial Intelligence Analysis of Celiac Disease Using an Autoimmune Discovery Transcriptomic Panel Highlighted Pathogenic Genes including BTLA.使用自身免疫发现转录组面板对乳糜泻进行人工智能分析,突出了包括BTLA在内的致病基因。
Healthcare (Basel). 2022 Aug 16;10(8):1550. doi: 10.3390/healthcare10081550.
7
Epidemiological, clinical, and histological presentation of celiac disease in Northwest China.中国西北地区乳糜泻的流行病学、临床和组织学表现。
World J Gastroenterol. 2022 Mar 28;28(12):1272-1283. doi: 10.3748/wjg.v28.i12.1272.
8
The Risk of Malignancies in Celiac Disease-A Literature Review.乳糜泻患者发生恶性肿瘤的风险——文献综述
Cancers (Basel). 2021 Oct 21;13(21):5288. doi: 10.3390/cancers13215288.
9
Enteropathy-Associated T cell Lymphoma.肠病相关 T 细胞淋巴瘤。
Curr Hematol Malig Rep. 2021 Apr;16(2):140-147. doi: 10.1007/s11899-021-00634-4. Epub 2021 May 19.
10
Refractory Celiac Disease.难治性乳糜泻
Curr Gastroenterol Rep. 2020 Mar 17;22(4):18. doi: 10.1007/s11894-020-0756-8.