Apolipoprotein(a) Phenotype, Albumin Clearance, and Plasma Levels of Lipoprotein(a) in Peritoneal Dialysis

Nephron ◽  
2001 ◽  
Vol 88 (2) ◽  
pp. 168-169 ◽  
Author(s):  
Eduard A. Iliescu ◽  
Santica M. Marcovina ◽  
Alexander R. Morton ◽  
Marlys L. Koschinsky
2018 ◽  
Vol 39 (suppl_1) ◽  
Author(s):  
E A Klesareva ◽  
O I Afanasieva ◽  
O A Razova ◽  
E A Utkina ◽  
M I Afanasieva ◽  
...  

2002 ◽  
Vol 22 (4) ◽  
pp. 492-499 ◽  
Author(s):  
Eduard A. Iliescu ◽  
Santica M. Marcovina ◽  
Alexander R. Morton ◽  
Miu Lam ◽  
Marlys L. Koschinsky

♦ Objective To examine the associations between lipoprotein(a) [Lp(a)] level, apolipoprotein(a) [apo(a)] phenotype, and patient mortality in peritoneal dialysis (PD) patients. ♦ Design Observational prospective study of prevalent PD patients. ♦ Setting Tertiary-care health sciences center. ♦ Patients 54 prevalent PD patients were followed prospectively for 24 months. ♦ Main Outcome Measures The exposures were Lp(a) level and apo(a) phenotype, designated by the apo(a) isoform size (number of kringle 4 repeats). Outcome was death from any cause. ♦ Results There were 24 deaths in 77.9 patient–years’ follow-up. The independent predictors of death in the multivariate survival analysis were age [relative risk (RR) = 1.03, p = 0.23], diabetes (RR = 3.00, p = 0.03), diastolic blood pressure ≤ 70 mmHg (RR = 2.94, p = 0.03), serum albumin (RR = 0.87, p < 0.01), and Lp(a) level (RR = 1.004, p < 0.01). There was strong inverse correlation of Lp(a) with apo(a) isoform size ( r = –0.62, p < 0.01). With Lp(a) removed from the model, apo(a) isoform size was a significant predictor of death (RR = 0.91, p = 0.0497). ♦ Conclusions Lipoprotein(a) level and apo(a) phenotype are associated with PD patient mortality. Measurement of Lp(a) level and apo(a) phenotype may be useful in clinical practice to identify patients at high risk for cardiovascular disease. Large prospective studies are needed to determine if a reversal of the increase in Lp(a) level associated with renal disease and dialysis is feasible and beneficial in reducing the risk of cardiovascular disease and mortality.


1995 ◽  
Vol 6 (1) ◽  
pp. 110-120
Author(s):  
F Kronenberg ◽  
P König ◽  
U Neyer ◽  
M Auinger ◽  
A Pribasnig ◽  
...  

Numerous studies have investigated lipoprotein(a) (Lp(a)) plasma concentrations in patients with ESRD, a patient group with an enormous risk for atherosclerosis. The reported differences in Lp(a) between controls and patients vary from a decrease of 49% to an increase of more than 1,000%. However, data are not consistent, mostly because of problems with statistical analysis, and only limited data are available for patients treated by continuous ambulatory peritoneal dialysis (CAPD). To estimate the significance of Lp(a) in ESRD and to demonstrate the statistical pitfalls concerning Lp(a) in case-control studies, a large multicenter study including 702 patients treated by either hemodialysis (HD) (N = 534) or CAPD (N = 168) was conducted, and results were compared with results from 256 healthy controls. Both patient groups showed significantly elevated Lp(a) levels in comparison with controls: 23.4 +/- 25.0 mg/dL (P < 0.005; HD) and 34.6 +/- 38.4 mg/dL (P < 0.0001; CAPD) versus 18.4 +/- 22.8 mg/dL (controls). CAPD patients showed significantly higher Lp(a) values than did patients treated by HD (P < 0.001). The difference between the two treatment groups possibly reflects an overproduction of Lp(a) to compensate for protein losses in CAPD patients. Both treatment groups included significantly more patients with Lp(a) values greater than the 75th percentile (25.6 mg/dL) of the control group (33.9 and 41.7% for HD and CAPD, respectively; P < 0.005). The higher Lp(a) values in patients were not explained by differences in isoform frequencies and the increase in Lp(a) was apolipoprotein(a) type specific: only patients with high-molecular-weight apolipoprotein(a) isoforms showed a significant elevation in Lp(a) levels. The increased plasma concentrations of Lp(a) may contribute to the high risk for atherosclerosis in ESRD, especially in patients treated by CAPD. Finally, it is believed that small sample sizes are responsible for the diverging results in Lp(a) literature.


2011 ◽  
Vol 57 (15) ◽  
pp. 1611-1621 ◽  
Author(s):  
Esther Merki ◽  
Mark Graham ◽  
Adam Taleb ◽  
Gregor Leibundgut ◽  
Xiaohong Yang ◽  
...  

1996 ◽  
Vol 97 (3) ◽  
pp. 858-864 ◽  
Author(s):  
V Mooser ◽  
M C Seabra ◽  
M Abedin ◽  
K T Landschulz ◽  
S Marcovina ◽  
...  

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