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. 2019 Nov;41(1):800-807.
doi: 10.1080/0886022X.2019.1659151.

Serum lipoprotein(a) and risk of hemorrhagic stroke among incident peritoneal dialysis patients: a large study from a single center in China

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Serum lipoprotein(a) and risk of hemorrhagic stroke among incident peritoneal dialysis patients: a large study from a single center in China

Yanbing Chen et al. Ren Fail. 2019 Nov.

Abstract

Background: This retrospective study investigated whether baseline serum lipoprotein(a) (Lp(a)) may predict subsequent stroke in patients under chronic peritoneal dialysis (PD). Methods: Eight hundred and sixty incident PD patients, treated from 1 November 2005 to 28 February 2017, were enrolled, and followed until discontinuation of PD, death, or 31 May 2017. Hemorrhagic or ischemic stroke was the primary outcome. The population was stratified by baseline serum Lp(a) tertile. The risk of each stroke subtype was analyzed using the Cox proportional hazard models. Adjustments were made for: age; gender; history of stroke and hypertension; systolic blood pressure; lipid-lowering, antiplatelet and antihypertensive medications; laboratory profiles including hemoglobin, serum albumin, calcium, triglyceride, total and low-density lipoprotein cholesterol; and apolipoprotein A1. Results: Among the 860 participants, 19.3% and 4.1% had diabetes mellitus and a history of stroke, respectively. The median baseline serum Lp(a) was 328 (172-585) mg/L. After 28 (14-41) months of follow-up, 33 (3.84%) and 12 (1.40%) patients developed hemorrhagic and ischemic stroke, respectively. Participants in the highest Lp(a) tertile had a significantly lower risk of hemorrhagic stroke compared with those in the lowest tertile (hazard ratio (HR) 0.3, 95% confidence interval (CI) 0.1-0.86; p = .026); the rates of ischemic stroke were comparable among the tertiles. Each 10 mg/L rise in serum Lp(a) was associated with a 2% (95% CI 0.96-1; p = .033) lower risk of hemorrhagic stroke. Conclusions: Among patients with incident PD, a higher serum Lp(a) level may predict a lower risk of hemorrhagic stroke.

Keywords: End-stage renal disease; hemorrhagic stroke; lipoprotein(a); peritoneal dialysis; stroke.

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Figures

Figure 1.
Figure 1.
A flowchart of study participant enrollment. CAPD: continuous ambulatory peritoneal dialysis; HD: hemodialysis.
Figure 2.
Figure 2.
Hemorrhagic stroke-free survival curves for patients treated with peritoneal dialysis stratified by serum lipoprotein(a) tertile.

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References

    1. Aronis KN, Zhao D, Hoogeveen RC, et al. . Associations of lipoprotein(a) levels with incident atrial fibrillation and ischemic stroke: the ARIC (Atherosclerosis Risk in Communities) Study. J Am Heart Assoc. 2017;6:pii: e007372. - PMC - PubMed
    1. Ishikawa S, Kotani K, Kario K, et al. . Inverse association between serum lipoprotein(a) and cerebral hemorrhage in the Japanese population. Thromb Res. 2013;131:e54–e58. - PubMed
    1. Kim H, Kim KH, Ahn SV, et al. . Risk of major cardiovascular events among incident dialysis patients: a Korean national population-based study. Int J Cardiol. 2015;198:95–101. - PubMed
    1. Fu J, Huang J, Lei M, et al. . Prevalence and impact on stroke in patients receiving maintenance hemodialysis versus peritoneal dialysis: a prospective observational study. PLoS One. 2015;10:e0140887. - PMC - PubMed
    1. Findlay M, MacIsaac R, MacLeod MJ, et al. . Renal replacement modality and stroke risk in end-stage renal disease-a national registry study. Nephrol Dial Transplant. 2018;33:1564–1571. - PubMed

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