Resolution of typical lipoprotein glomerulopathy by intensive lipid-lowering therapy
Resolution of typical lipoprotein glomerulopathy by intensive lipid-lowering therapy
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DOI:
10.1053/ajkd.2003.50016
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发表时间:
2003-01-01
影响因子:
13.2
通讯作者:
Taguma, Y
中科院分区:
文献类型:
--
作者:
Ieiri, N;Hotta, O;Taguma, Y
Lipoprotein glomerulopathy (LPG), characterized by glomerular lipoprotein thrombi, presumably composed of abnormal apolipoprotein E (apoE), leads to a progressive decline in renal function and eventually results in end-stage renal failure. A successful treatment for LPG has not yet been established. The authors treated a 36-year-old woman with LPG and exhibiting a nephrotic syndrome using an intensive lipid-lowering therapy consisting of fenofibrate (300 mg), niceritrol (750 mg), ethyl-icosapentate (1,800 mg), and probucol (500 mg). After the start of treatment, a remarkable decrease in urinary protein excretion and improvement in the hyperlipidemia were obtained; proteinuria was no longer detected 11 months after the initiation of treatment. A second biopsy performed 11 months after the initiation of treatment showed the complete disappearance of the lipoprotein thrombi that had been observed in a diffuse and global manner in the first renal biopsy. These findings suggest that typical LPG could be regressed if the abnormal lipoproteinemia is controlled sufficiently.