TY - JOUR
T1 - Favorable therapeutic efficacy of low-density lipoprotein apheresis for nephrotic syndrome with impaired renal function
AU - Muso, Eri
AU - Sakai, Soichi
AU - Ogura, Youske
AU - Yukawa, Susumu
AU - Nishizawa, Yoshiki
AU - Yorioka, Noriaki
AU - Saito, Takao
AU - Mune, Masatoshi
AU - Sugiyama, Satoshi
AU - Iino, Yasuhiko
AU - Hirano, Tsutomu
AU - Hattori, Motoshi
AU - Watanabe, Tsuyoshi
AU - Yokoyama, Hitoshi
AU - Sato, Hiroshi
AU - Uchida, Shunya
AU - Wada, Takashi
AU - Shoji, Tetsuo
AU - Oda, Hiroaki
AU - Mori, Kiyoshi
AU - Kimura, Hideki
AU - Ito, Osamu
AU - Nishiyama, Akira
AU - Maruyama, Shoichi
AU - Inagi, Reiko
AU - Fujimoto, Shoichi
AU - Tsukamoto, Tatsuo
AU - Suzuki, Yusuke
AU - Honda, Hirokazu
AU - Babazono, Tetsuya
AU - Tsuruya, Kazuhiko
AU - Yuzawa, Yukio
N1 - Publisher Copyright:
© 2021 The Authors. Therapeutic Apheresis and Dialysis published by John Wiley & Sons Australia, Ltd on behalf of International Society for Apheresis, Japanese Society for Apheresis, and Japanese Society for Dialysis Therapy.
PY - 2022/2
Y1 - 2022/2
N2 - Many reports have shown the therapeutic efficacy of LDL apheresis (LDL-A) in drug-resistant nephrotic syndrome (NS) for improvement of heavy proteinuria and severely impaired renal function. To obtain comprehensive results in a large number of cases, a post hoc analysis of the Prospective Observational survey on the Long-Term Effects of the LDL-Apheresis on the Drug Resistant Nephrotic Syndrome (POLARIS) study was performed by stratifying enrolled cases according to the pretreatment estimated glomerular filtration rate (eGFR) levels indicating normal (N) (≥60 ml/min/1.73 m2), moderately impaired (M) (≥30 to <60 ml/min/1.73 m2), and severely impaired (S) (<30 ml/min/1.73 m2) renal function. Significant improvements of proteinuria and renal function were found in Group N and, most interestingly, in Group M. A tendency for improvement in proteinuria was found in Group S. Most cases in all groups had not entered end-stage renal disease at 2 years after LDL-A treatment. These results suggest that LDL-A has therapeutic efficacy even in cases in which renal function has declined to 30 ml/min/1.73 m2.
AB - Many reports have shown the therapeutic efficacy of LDL apheresis (LDL-A) in drug-resistant nephrotic syndrome (NS) for improvement of heavy proteinuria and severely impaired renal function. To obtain comprehensive results in a large number of cases, a post hoc analysis of the Prospective Observational survey on the Long-Term Effects of the LDL-Apheresis on the Drug Resistant Nephrotic Syndrome (POLARIS) study was performed by stratifying enrolled cases according to the pretreatment estimated glomerular filtration rate (eGFR) levels indicating normal (N) (≥60 ml/min/1.73 m2), moderately impaired (M) (≥30 to <60 ml/min/1.73 m2), and severely impaired (S) (<30 ml/min/1.73 m2) renal function. Significant improvements of proteinuria and renal function were found in Group N and, most interestingly, in Group M. A tendency for improvement in proteinuria was found in Group S. Most cases in all groups had not entered end-stage renal disease at 2 years after LDL-A treatment. These results suggest that LDL-A has therapeutic efficacy even in cases in which renal function has declined to 30 ml/min/1.73 m2.
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U2 - 10.1111/1744-9987.13694
DO - 10.1111/1744-9987.13694
M3 - Article
C2 - 34057286
AN - SCOPUS:85108384269
SN - 1744-9979
VL - 26
SP - 220
EP - 228
JO - Therapeutic Apheresis and Dialysis
JF - Therapeutic Apheresis and Dialysis
IS - 1
ER -