Lipid profile in chronic allograft nephropathy

被引:3
|
作者
Sahin, S
Sahin, GM
Kantarci, G
Ergin, H
Sezgin, O
机构
[1] SB Goztepe Training Hosp, Dept Nephrol, Istanbul, Turkey
[2] SB Goztepe Training Hosp, Dept Endocrinol, Istanbul, Turkey
关键词
D O I
10.1016/j.transproceed.2005.12.091
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic allograft nephropathy (CAN) represents the cumulative and incremental damage to nephrons by time-dependent immunologic and nonimmunologic causes. Hyperlipidemia is one nonimmunologic mechanism that promotes injury and poor function in a renal transplant. The aim of our study was to determine the effect of lipid profiles on CAN among renal transplant recipients. We retrospectively evaluated 53 renal transplant recipients who were classified according to the presence of CAN: CAN+ = 28 (18 males, 1.0 females) constituted the study group, whereas those with stable graft function CAN- 25 (14 males, 11 females) were the control group. Biochemical parameters included serum urea, creatinine, total cholesterol, triglyceride, HDL cholesterol, LDL cholesterol, apolipoprotein A1 (ApoA1), apolipoprotein B (ApoB), lipoprotein (a), homocysteine, and high-sensitive CRP (hs CRP). Angiotensin-converting enzyme inhibitor (ACEI) and/or angiotensin receptor blocker (ARB) use was significantly greater among the CAN+ group compared with the controls (P = .02, P = .04). Also, higher serum creatinine levels were observed in the CAN+ group (1.49 vs 1.22 mg/dL, P = .002), whereas serum levels of total cholesterol, triglyceride, hs CRP, and albumin were similar in both groups. The levels of ApoA1, ApoB, and lipoprotein (a) were similar, whereas the LDL/HDL cholesterol ratio and homocysteine levels were significantly higher in the CAN+ group (P = .04, P = .04). In conclusion, the LDL/HDL ratio may have a positive impact on CAN and may be used as a parameter during patient follow-up.
引用
下载
收藏
页码:477 / 479
页数:3
相关论文
共 50 条
  • [11] Glomerular hyperfiltration, intrarenal hemodynamics, and chronic allograft nephropathy:: Physiopathology of chronic allograft nephropathy
    Solà, R
    Paredes, D
    Antonijoan, RM
    Estorch, M
    Vila, LP
    Guirado, LL
    Diaz, JM
    Gich, I
    Barbanoj, MJ
    TRANSPLANTATION PROCEEDINGS, 2002, 34 (01) : 340 - +
  • [12] Chronic Allograft Nephropathy (Chronic Allograft Damage): Can It Be Avoided?
    Yilmaz S.
    Current Transplantation Reports, 2014, 1 (2) : 91 - 99
  • [13] Chronic Allograft Nephropathy with Proteinuria
    Etta, Praveen
    Madhavi, Thatipamula
    INDIAN JOURNAL OF TRANSPLANTATION, 2021, 15 (03) : 282 - 283
  • [14] Senescence in chronic allograft nephropathy
    Pena, Maria del Pilar Sosa
    Lopez-Soler, Reynold
    Melendez, J. Andres
    AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2018, 315 (04) : F880 - F889
  • [15] Chronic renal allograft nephropathy
    Morozumi K.
    Uchida K.
    Takeda A.
    Clinical and Experimental Nephrology, 2000, 4 (2) : 87 - 98
  • [16] Pathogenesis of chronic allograft nephropathy
    Paul, LC
    CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 1998, 7 (06): : 635 - 637
  • [17] Chronic allograft nephropathy - Reply
    Nankivell, BJ
    Chapman, JR
    NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (12): : 1255 - 1256
  • [18] Chronic allograft nephropathy: An update
    Paul, LC
    KIDNEY INTERNATIONAL, 1999, 56 (03) : 783 - 793
  • [19] Sirolimus in chronic allograft nephropathy
    Garvey, J. P.
    Chotirmall, Sanjay Haresh
    Curran, Simon
    Conlon, Peter
    Donohoe, John
    Walshe, Joseph
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2006, 21 : 268 - 268
  • [20] Sirolimus in chronic allograft nephropathy
    Wu, MJ
    Shu, KH
    Cheng, CH
    Chen, CH
    TRANSPLANTATION PROCEEDINGS, 2004, 36 (07) : 2053 - 2055