Myocardial Iron Deficiency in Hemodialysis-Dependent End-Stage Renal Disease Patients Undergoing Oral Iron Therapy
Myocardial Iron Deficiency in Hemodialysis-Dependent End-Stage Renal Disease Patients Undergoing Oral Iron Therapy
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接受口服铁治疗的血液透析依赖性终末期肾病患者的心肌缺铁
DOI:
10.1016/j.jacc.2017.09.013
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发表时间:
2017
影响因子:
24
通讯作者:
Guo Ying-kun
中科院分区:
文献类型:
--
作者:
Xu Hua-yan;Yang Zhi-gang;Li Rui;Shi Ke;Zhang Yi;Li Zhen-lin;Xia Chun-chao;Peng Wan-lin;Chen Qing-yong;Guo Ying-kun
Iron deficiency is the most common complication and the main cause of anemia in patients with hemodialysis-dependent end-stage renal disease (ESRD). There are possible relations among iron deficiency, cardiac failure, renal failure, and anemia, termed as the cardio-renal-anemia iron deficiency syndrome (1). Correction of this iron deficiency is necessary to improve anemia and reduce the risk of cardiovascular complications in patients with ESRD. Oral iron therapy is relatively inexpensive and widely used, but the evidence for the clinical benefits of using oral iron is limited and controversial (2). Clinically, iron deficiency is usually identified on serum ferritin (SF) because of its ease of use and wide availability, and stored levels are often determined on the liver iron content. However, there is evidence indicating that SF and liver iron are poor indicators for tissue iron in some vital organs such as the heart (3). Thus, quantitative assessment of myocardial iron levels in patients with hemodialysis-dependent ESRD may be useful for iron management, even for cases in which SF levels are within or higher than the normal range. In this study, we aimed to assess myocardial iron levels in patients with hemodialysis-dependent ESRD taking oral iron using cardiac magnetic resonance (CMR) T2* mapping, and further, to determine the predictive value of T2* for left ventricular (LV) dysfunction.We included 61 patients with ESRD (age 55.39±15.96 years, 23 men) and 29 normal control subjects with similar age and sex distributions (age 52.58±13.40 years, 12 men) in our institution. All patients with ESRD were treated with regular dialysis (twice weekly) and routine oral iron drugs (polysaccharide iron complex, 600 mg/day). The 8 echo T2* source images were obtained in a series of basal, middle, and apical short-axis slices (8 echoes, echo time range: 2.59 to 15.68 ms; repetition time: 816.40 ms; slice thickness: 8 mm; field of view: 357.50× 440.00 mm; flip angle: 40) on a 3.0-T magnetic resonance scanner (Skyra, Siemens Medical Solutions, Erlangen, Germany), and were used to generate the T2* map and values. LV T2* mapping and function were analyzed using offline software (cmr42, Circle Cardiovascular Imaging Inc., Calgary, Alberta, Canada).