Low triiodothyronine and cardiomyopathy in patients with end-stage renal disease

被引:49
作者
Zoccali, Carmine
Benedetto, Francesco
Mallamaci, Francesca
Tripepi, Giovanni
Cutrupi, Sebastiano
Pizzini, Patrizia
Malatino, Lorenzo Salvatore
Bonanno, Graziella
Seminara, Giuseppe
机构
[1] Ki Point Gransial Srl, CNR, Ist Biomed Epidemiol Clin & Fisiopatol, IBIM,Malattie Renal & Ipertens Arteriosa, I-89125 Reggio Di Calabria, Italy
[2] Div Nephrol, Reggio Di Calabria, Italy
[3] Riuniti Hosp, Cardiol Unit, Reggio Di Calabria, Italy
[4] Univ Catania, Dept Internal Med L Condorelli, Catania, Italy
关键词
dialysis; left ventricular hypertrophy; systolic dysfunction; subclinical hypothyroidism; inflammation;
D O I
10.1097/01.hjh.0000244954.62362.8f
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objectives and methods Low free plasma triiodothyronine (fT3) is associated with inflammation and cardiovascular damage in patients with end-stage renal disease (ESRD). We investigated the relationship between fT3, left ventricular systolic function and left ventricular mass in a group of 234 dialysis patients, and modelled the association between fT3 and cardiomyopathy in statistical analyses including both direct (interleukin-6 and C-reactive protein) and inverse (serum albumin) acute phase inflammation markers. Results Plasma fT3 concentration in dialysis patients was significantly (P < 0.001) reduced in comparison with healthy participants and clinically euthyroid patients with normal renal function. Left ventricular systolic function was depressed (P <= 0.003) and left ventricular mass increased (P < 0.001) in patients in the first fT3 quartile as compared with patients in other quartiles. In multiple regression analyses these associations remained significant also after adjustment for Framingham risk factors and antihypertensive therapy (P <= 0.01), and for risk factors peculiar to ESRD (P = 0.03). Adjustments for interleukin-6 or for albumin, however, abrogated these relationships. Conclusions Low triiodothyronine is associated with left ventricular dysfunction and left ventricular hypertrophy in ESRD patients. These associations appear largely mediated by inflammation. Low fT3 may be an intermediate mechanism implicated in the adverse cardiac effects of inflammation in patients with ESRD.
引用
收藏
页码:2039 / 2046
页数:8
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