• 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

心力衰竭患者缺铁纠正前后器官铁的磁共振成像。

Magnetic resonance imaging of organ iron before and after correction of iron deficiency in patients with heart failure.

机构信息

Department of Cardiology and Pneumology, University of Göttingen Medical Center, Göttingen, Germany.

German Center for Cardiovascular Research (DZHK), Partner site Göttingen, Göttingen, Germany.

出版信息

ESC Heart Fail. 2023 Jun;10(3):1847-1859. doi: 10.1002/ehf2.14329. Epub 2023 Mar 12.

DOI:10.1002/ehf2.14329
PMID:36907649
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10192268/
Abstract

AIMS

Intravenous iron therapy (IVIT) is known to improve functional status in chronic heart failure (CHF) patients. The exact mechanism is not completely understood. We correlated magnetic resonance imaging (MRI) patterns of T2* iron signal in various organs to systemic iron and exercise capacity (EC) in CHF before and after IVIT.

METHODS AND RESULTS

We prospectively analysed 24 patients with systolic CHF for T2* MRI pattern of the left ventricle (LV), small and large intestines, spleen, liver, skeletal muscle, and brain for iron. In 12 patients with iron deficiency (ID), we restored iron deficit by IVIT using ferric carboxymaltose. The effects after 3 months were analysed by spiroergometry and MRI. Patients with vs. without ID showed lower blood ferritin, haemoglobin (76 ± 63 vs. 196 ± 82 μg/L and 12.3 ± 1.1 vs. 14.2 ± 1.1 g/dL, all P < 0.002), and in trend a lower transferrin saturation (TSAT) (19.1 [13.1; 28.2] vs. 25.1 [21.3; 29.1] %, P = 0.05). Spleen and liver iron was lower as expressed by higher T2* value (71.8 [66.4; 93.1] vs. 36.9 [32.9; 51.7] ms, P < 0.002 and 33.5 ± 5.9 vs. 28.8 ± 3.9 ms, and P < 0.03). There was a strong trend for a lower cardiac septal iron content in ID (40.6 [33.0; 57.3] vs. 33.7 [31.3; 40.2] ms, P = 0.07). After IVIT, ferritin, TSAT, and haemoglobin increased (54 [30; 104] vs. 235 [185; 339] μg/L, 19.1 [13.1; 28.2] vs. 25.0 [21.0; 33.7] %, 12.3 ± 1.1 vs. 13.3 ± 1.3 g/L, all P < 0.04). Peak VO improved (18.2 ± 4.2 vs. 20.9 ± 3.8 mL/min/kg , P = 0.05). Higher peak VO at anaerobic threshold was associated with higher blood ferritin, reflecting higher metabolic exercise capacity after therapy (r = 0.9, P = 0.0009). Increase in EC was associated with haemoglobin increase (r = 0.7, P = 0.034). LV iron increased by 25.4% (48.5 [36.2; 64.8] vs. 36.2 [32.9; 41.9] ms, P < 0.04). Spleen and liver iron increased by 46.4 and 18.2%, respectively (71.8 [66.4; 93.1] vs. 38.5 [22.4; 76.9] ms, P < 0.04 and 33.5 ± 5.9 vs. 27.4 ± 8.6 ms, P < 0.007). Iron in skeletal muscle, brain, intestine, and bone marrow remained unchanged (29.6 [28.6; 31.2] vs. 30.4 [29.7; 30.7] ms, P = 0.7, 81.0 ± 6.3 vs. 82.9 ± 9.9 ms, P = 0.6, 34.3 ± 21.4 vs. 25.3 ± 14.1 ms, P = 0.2, 9.4 [7.5; 21.8] vs. 10.3 [6.7; 15.7] ms, P = 0.5 and 9.8 ± 1.5 vs. 13.7 ± 8.9 ms, P = 0.1).

CONCLUSIONS

CHF patients with ID showed lower spleen, liver, and in trend lower cardiac septal iron. After IVIT, iron signal of the left ventricle as well as spleen and liver increased. Improvement in EC was associated with increase in haemoglobin after IVIT. In ID, liver, spleen, and brain but not heart iron were associated with markers of systemic ID.

摘要

目的

静脉铁治疗(IVIT)已知可改善慢性心力衰竭(CHF)患者的功能状态。确切的机制尚不完全清楚。我们将铁磁共振成像(MRI)T2*铁信号的各种器官模式与 CHF 患者 IVIT 前后的系统铁和运动能力(EC)相关联。

方法和结果

我们前瞻性地分析了 24 例收缩性 CHF 患者的左心室(LV)、小肠、大肠、脾脏、肝脏、骨骼肌和大脑的 T2* MRI 模式。在 12 例缺铁(ID)患者中,我们使用羧基麦芽糖铁通过 IVIT 来纠正缺铁。在 3 个月后通过测功计和 MRI 分析效果。与 ID 患者相比,无 ID 患者的血铁蛋白、血红蛋白(76±63 vs. 196±82μg/L 和 12.3±1.1 vs. 14.2±1.1g/dL,均 P<0.002)和转铁饱和度(TSAT)较低(19.1[13.1; 28.2] vs. 25.1[21.3; 29.1]%,P=0.05)。脾脏和肝脏铁的 T2*值较高,表明铁含量较低(71.8[66.4; 93.1] vs. 36.9[32.9; 51.7]ms,P<0.002 和 33.5±5.9 vs. 28.8±3.9ms,P<0.03)。ID 患者的心脏间隔铁含量也有较低的趋势(40.6[33.0; 57.3] vs. 33.7[31.3; 40.2]ms,P=0.07)。IVIT 后,铁蛋白、TSAT 和血红蛋白升高(54[30; 104] vs. 235[185; 339]μg/L,19.1[13.1; 28.2] vs. 25.0[21.0; 33.7]%,12.3±1.1 vs. 13.3±1.3g/L,均 P<0.04)。峰值 VO 改善(18.2±4.2 vs. 20.9±3.8mL/min/kg,P=0.05)。更高的无氧阈峰值 VO 与更高的血铁蛋白相关,反映出治疗后更高的代谢运动能力(r=0.9,P=0.0009)。EC 的增加与血红蛋白的增加相关(r=0.7,P=0.034)。LV 铁增加了 25.4%(48.5[36.2; 64.8] vs. 36.2[32.9; 41.9]ms,P<0.04)。脾脏和肝脏铁分别增加了 46.4%和 18.2%(71.8[66.4; 93.1] vs. 38.5[22.4; 76.9]ms,P<0.04 和 33.5±5.9 vs. 27.4±8.6ms,P<0.007)。骨骼肌、大脑、肠道和骨髓中的铁含量保持不变(29.6[28.6; 31.2] vs. 30.4[29.7; 30.7]ms,P=0.7,81.0±6.3 vs. 82.9±9.9ms,P=0.6,34.3±21.4 vs. 25.3±14.1ms,P=0.2,9.4[7.5; 21.8] vs. 10.3[6.7; 15.7]ms,P=0.5 和 9.8±1.5 vs. 13.7±8.9ms,P=0.1)。

结论

ID 的 CHF 患者的脾脏、肝脏和心脏中隔的铁含量较低。IVIT 后,左心室、脾脏和肝脏的铁信号增加。IVIT 后血红蛋白增加与 EC 改善相关。在 ID 中,肝脏、脾脏和大脑中的铁,但不是心脏铁,与全身 ID 的标志物相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/1e07197c563d/EHF2-10-1847-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/d03ac3edb760/EHF2-10-1847-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/ffbe7f76c0b1/EHF2-10-1847-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/d9041c75716c/EHF2-10-1847-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/990974b57a2d/EHF2-10-1847-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/43f735160d56/EHF2-10-1847-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/be7b202503c1/EHF2-10-1847-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/015494db6bdf/EHF2-10-1847-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/1e07197c563d/EHF2-10-1847-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/d03ac3edb760/EHF2-10-1847-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/ffbe7f76c0b1/EHF2-10-1847-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/d9041c75716c/EHF2-10-1847-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/990974b57a2d/EHF2-10-1847-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/43f735160d56/EHF2-10-1847-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/be7b202503c1/EHF2-10-1847-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/015494db6bdf/EHF2-10-1847-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/10192268/1e07197c563d/EHF2-10-1847-g008.jpg

相似文献

1
Magnetic resonance imaging of organ iron before and after correction of iron deficiency in patients with heart failure.心力衰竭患者缺铁纠正前后器官铁的磁共振成像。
ESC Heart Fail. 2023 Jun;10(3):1847-1859. doi: 10.1002/ehf2.14329. Epub 2023 Mar 12.
2
In Search of Optimal Criteria for Iron Deficiency in CHF Patients. Post-hoc Analysis of the Study "Prevalence of Iron Deficiency in Patients With Chronic Heart Failure in the Russian Federation (ID-CHF-RF)".探寻 CHF 患者缺铁的最佳标准。研究“俄罗斯联邦慢性心力衰竭患者缺铁患病率(ID-CHF-RF)”的事后分析。
Kardiologiia. 2024 Sep 30;64(9):16-27. doi: 10.18087/cardio.2024.9.n2732.
3
Iron deficiency is an independent risk factor of increased myocardial energy expenditure in chronic heart failure patients.缺铁是慢性心力衰竭患者心肌能量消耗增加的独立危险因素。
Ann Palliat Med. 2021 Dec;10(12):12061-12071. doi: 10.21037/apm-21-2297.
4
Intravenous iron therapy improves the hypercapnic ventilatory response and sleep disordered breathing in chronic heart failure.静脉铁治疗可改善慢性心力衰竭患者的高碳酸血症通气反应和睡眠呼吸障碍。
Eur J Heart Fail. 2022 Oct;24(10):1940-1949. doi: 10.1002/ejhf.2628. Epub 2022 Aug 8.
5
Influence of serum transferrin concentration on diagnostic criteria for iron deficiency in chronic heart failure.血清转铁蛋白浓度对慢性心力衰竭铁缺乏症诊断标准的影响。
ESC Heart Fail. 2023 Oct;10(5):2826-2836. doi: 10.1002/ehf2.14438. Epub 2023 Jul 3.
6
Iron deficiency predicts impaired exercise capacity in patients with systolic chronic heart failure.缺铁预测收缩性慢性心力衰竭患者运动能力受损。
J Card Fail. 2011 Nov;17(11):899-906. doi: 10.1016/j.cardfail.2011.08.003.
7
Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long-term study.铁羧基麦芽糖在肺动脉高压伴缺铁患者中的长期研究。
J Cachexia Sarcopenia Muscle. 2021 Dec;12(6):1501-1512. doi: 10.1002/jcsm.12764. Epub 2021 Sep 9.
8
Re-defining iron deficiency in patients with heart failure.重新定义心力衰竭患者的缺铁症。
Expert Rev Cardiovasc Ther. 2022 Aug;20(8):667-681. doi: 10.1080/14779072.2022.2100349. Epub 2022 Jul 13.
9
Iron deficiency is related to low functional outcome in patients at early rehabilitation after acute stroke.缺铁与急性脑卒中后早期康复患者的功能结局不良有关。
J Cachexia Sarcopenia Muscle. 2022 Apr;13(2):1036-1044. doi: 10.1002/jcsm.12927. Epub 2022 Feb 14.
10
Effect of Ferric Carboxymaltose on Exercise Capacity in Patients With Chronic Heart Failure and Iron Deficiency.羧麦芽糖铁对慢性心力衰竭合并缺铁患者运动能力的影响
Circulation. 2017 Oct 10;136(15):1374-1383. doi: 10.1161/CIRCULATIONAHA.117.027497. Epub 2017 Jul 12.

引用本文的文献

1
Iron deficiency in heart failure: Epidemiology, diagnostic criteria and treatment modalities.心力衰竭中的缺铁:流行病学、诊断标准及治疗方式
ESC Heart Fail. 2025 Apr;12(2):723-726. doi: 10.1002/ehf2.15157. Epub 2024 Oct 30.
2
Unveiling the invisible: Is there a role of CMR in biopsy-negative graft dysfunction post-heart transplantation?揭示无形之物:心脏移植后活检阴性移植物功能障碍中,心脏磁共振成像有作用吗?
ESC Heart Fail. 2024 Oct;11(5):2484-2486. doi: 10.1002/ehf2.14994. Epub 2024 Jul 23.
3
Interplay of the heart, spleen, and bone marrow in heart failure: the role of splenic extramedullary hematopoiesis.

本文引用的文献

1
Myocardial Iron Deficiency and Mitochondrial Dysfunction in Advanced Heart Failure in Humans.心肌铁缺乏和人类晚期心力衰竭中的线粒体功能障碍。
J Am Heart Assoc. 2022 Jun 7;11(11):e022853. doi: 10.1161/JAHA.121.022853. Epub 2022 Jun 3.
2
Myocardial iron overload by cardiovascular magnetic resonance native segmental T1 mapping: a sensitive approach that correlates with cardiac complications.心血管磁共振原生节段 T1 映射显示心肌铁过载:一种与心脏并发症相关的敏感方法。
J Cardiovasc Magn Reson. 2021 Jun 14;23(1):70. doi: 10.1186/s12968-021-00765-w.
3
Ferric carboxymaltose for iron deficiency at discharge after acute heart failure: a multicentre, double-blind, randomised, controlled trial.
心力衰竭中心、脾、骨髓的相互作用:脾髓外造血的作用。
Heart Fail Rev. 2024 Sep;29(5):1049-1063. doi: 10.1007/s10741-024-10418-6. Epub 2024 Jul 10.
4
Identification of three mechanistic pathways for iron-deficient heart failure.鉴定缺铁性心力衰竭的三种机制途径。
Eur Heart J. 2024 Jul 9;45(26):2281-2293. doi: 10.1093/eurheartj/ehae284.
5
Iron deficiency and supplementation in heart failure.心力衰竭中的铁缺乏与补充。
Nat Rev Cardiol. 2024 Jul;21(7):463-486. doi: 10.1038/s41569-024-00988-1. Epub 2024 Feb 7.
6
Pathophysiology and Treatment Opportunities of Iron Deficiency in Heart Failure: Is There a Need for Further Trials?心力衰竭中铁缺乏的病理生理学和治疗机会:是否需要进一步的试验?
Curr Heart Fail Rep. 2023 Aug;20(4):300-307. doi: 10.1007/s11897-023-00611-3. Epub 2023 Jul 10.
铁羧基麦芽糖治疗急性心力衰竭出院后缺铁:一项多中心、双盲、随机、对照试验。
Lancet. 2020 Dec 12;396(10266):1895-1904. doi: 10.1016/S0140-6736(20)32339-4. Epub 2020 Nov 13.
4
Short-term changes in left and right systolic function following ferric carboxymaltose: a substudy of the Myocardial-IRON trial.羧基麦芽糖铁治疗后左右心室收缩功能的短期变化:心肌铁试验的一项子研究
ESC Heart Fail. 2020 Dec;7(6):4222-4230. doi: 10.1002/ehf2.13053. Epub 2020 Oct 11.
5
Overdosing on iron: Elevated iron and degenerative brain disorders.铁过量:铁升高与退行性脑疾病。
Exp Biol Med (Maywood). 2020 Oct;245(16):1444-1473. doi: 10.1177/1535370220953065. Epub 2020 Sep 2.
6
Age-Related Changes and Sex-Related Differences in Brain Iron Metabolism.脑铁代谢的年龄相关性变化和性别相关性差异。
Nutrients. 2020 Aug 27;12(9):2601. doi: 10.3390/nu12092601.
7
Cardiac iron concentration in relation to systemic iron status and disease severity in non-ischaemic heart failure with reduced ejection fraction.非缺血性射血分数降低心力衰竭中心脏铁浓度与全身铁状态和疾病严重程度的关系。
Eur J Heart Fail. 2020 Nov;22(11):2038-2046. doi: 10.1002/ejhf.1781. Epub 2020 Mar 10.
8
Noninvasive Imaging Estimation of Myocardial Iron Repletion Following Administration of Intravenous Iron: The Myocardial-IRON Trial.静脉铁剂给药后心肌铁补充的无创影像学评估:心肌铁剂试验。
J Am Heart Assoc. 2020 Feb 18;9(4):e014254. doi: 10.1161/JAHA.119.014254. Epub 2020 Feb 13.
9
Role of iron metabolism in heart failure: From iron deficiency to iron overload.铁代谢在心力衰竭中的作用:从缺铁到铁过载。
Biochim Biophys Acta Mol Basis Dis. 2019 Jul 1;1865(7):1925-1937. doi: 10.1016/j.bbadis.2018.08.030. Epub 2018 Aug 26.
10
Iron and the heart: A paradigm shift from systemic to cardiomyocyte abnormalities.铁与心脏:从系统性异常到心肌细胞异常的范式转变。
J Cell Physiol. 2019 Dec;234(12):21613-21629. doi: 10.1002/jcp.28820. Epub 2019 May 20.