- Open Access
Apolipoprotein B/apolipoprotein A1 ratio and mortality among incident peritoneal dialysis patients
© The Author(s). 2018
- Received: 17 March 2018
- Accepted: 4 May 2018
- Published: 17 May 2018
To investigate the association between the ratio of apolipoprotein B (apo B) / apolipoprotein A1 (apo A1) with all-cause mortality and cardiovascular events in peritoneal dialysis (PD) patients.
Eight hundred and sixty incident PD patients were enrolled from November 1, 2005, to February 28, 2017, and followed until May 31, 2017. Outcomes were all-cause mortality and cardiovascular events. Associations between the apo B/apo A1 ratio with all-cause mortality and cardiovascular events were evaluated using multivariable-adjusted Cox models.
Of the 860 patients, the mean age was 49.9 ± 14.5 years, 57.6% were men, and 19.3% were diabetic patients. The median apo B/apo A1 ratio was 0.65 (range: 0.22–2.24). During a median follow-up period of 27 months (interquartile range, 13 – 41 months), 202 deaths, and 145 cardiovascular events were recorded. After adjustment for age, sex, body mass index, diabetes, cardiovascular disease, systolic blood pressure, total Kt/V, estimated glomerular filtration rate, hemoglobin level, neutrophil to lymphocyte ratio and albumin, triglyceride, and cholesterol, as well as the use of lipid-lowering agents, the highest apo B/apo A1 ratio tertile was significantly associated with a hazard ratio for all-cause mortality of 1.60 (95% CI: 1.02 to 2.49, P = 0.040) and for cardiovascular events of 2.04 (95% CI: 1.21 to 3.44, P = 0.008).
An increased apo B/apo A1 ratio was independently associated with all-cause mortality and cardiovascular events in PD patients.
- Cardiovascular event
- Cohort study
- Peritoneal dialysis
Peritoneal dialysis (PD) patients have an increased risk of morbidity and mortality associated with cardiovascular disease (CVD), which is, at least in part, due to lipid abnormalities, typically called uremic dyslipidemia . Patients typically present with a decrease of the high-density lipoprotein cholesterol (HDL-C), and an increase of triglyceride (TG) and lipoprotein (a) [Lp (a)], with relatively normal or even lower levels of low-density lipoprotein cholesterol (LDL-C) .
LDL-C is widely recognized as the major atherogenic lipoprotein and is considered the primary therapeutic target for coronary heart disease . Furthermore, multiple lines of evidence indicate that other TG-rich lipoproteins, including intermediate density lipoprotein (IDL) or very low-density lipoprotein (VLDL) carry atherogenic potential as well . It has been reported that approximately 50% of patients with abnormalities of atherogenic lipoprotein had an increased risk for the development of CVD . This led to the consideration of non-HDL cholesterol as another important target for hyperlipidemia treatment. It is well known that, lipid-transporting apolipoprotein is an essential structural component of the lipoprotein cholesterol , VLDL, IDL and LDL cholesterol can each carry only a single apolipoprotein B (apo B)  and this characteristic can be used to reliably reflected the number of atherogenic lipoproteins in the plasma. In contrast, apo A1 has a strong association with HDL levels and accounts for approximately 60-70% of the total apolipoproteins in HDL-C, the plasma content of apo A1 represents the total of antiatherogenic particles . Therefore, the ratio of apo B to apo A1 (apo B/apo A1) reflects the balance of proatherogenic and antiatherogenic particles.
Recently, Sato et al.  indicated that a higher ratio of the apo B/apo A1 was associated with higher risk of all-cause and CVD-related mortality in patients on hemodialysis (HD). However, the lipid profile of PD patients was different from HD patients. In particular the lipid profile is more atherogenic in nature with more altered dyslipidemia when compared with those in HD patients . Moreover, the association between the apo B/apo A1 ratio and mortality in PD patients remains uncertain. Therefore, we hypothesized that a higher ratio of apo B/apo A1 is a critical parameter to predict the risk of cardiovascular events and all-cause mortality in PD patients. In this longitudinal cohort study, we assessed the associations between the apo B/apo A1 ratio with all-cause mortality and cardiovascular events in PD patients, and followed the patients for a median of 27 months at our PD center.
Study population and data collection
We studied all incident patients who used PD as their first renal replacement treatment modality and were followed up at the PD center of The First Affiliated Hospital, Nanchang University, Jiangxi, China from November 1, 2005, to February 28, 2017. Inclusion criteria were age ≥ 18 years at the start of PD and survival for at least 90 days from the first PD therapy. The patients who were catheterized in other hospitals, transferred from permanent HD, or failed renal transplantation were excluded in this study. The study was conducted in compliance with the ethical principles of the Helsinki Declaration (https://jamanetwork.com/journals/jama/fullarticle/1760318) and approved by the Human Ethics Committees of Nanchang University.
All patients were followed up until cessation of PD, death, or May 31, 2017. Baseline demographic data included age, sex, primary cause of end-stage renal disease (ESRD), and presence of diabetes and CVD. Clinical and biochemical data at the initiation of PD included body mass index, blood pressure, medication use, hemoglobin, serum albumin, serum creatinine, blood urea nitrogen, total cholesterol (CHOL), TG, HDL-C, LDL-C, Apo B, Apo A1, Lp (a). Immunoturbidimetric method was used to measure apo B and apo A1 concentrations. All baseline data were obtained during the first 1–3 months of PD. Baseline residual renal function was assessed by eGFR using the Chronic Kidney Disease Epidemiology Collaboration creatinine equation. Cardiovascular events were defined by the first occurrence of myocardial infarction, stroke, heart failure, hospitalization for unstable angina, peripheral vascular event, sudden death, death associated with a cardiovascular procedure, or death due to aneurysm dissection or rupture, fatal pulmonary embolism, or death due to other or unknown cardiovascular cause  after the onset of PD, and was determined by the PD follow-up panel composed of PD primary nurses and professors.
Patients with apo B/apo A1 ratio were classified into tertiles (Ts): T1 ≤ 0.545, T2 = 0.545-0.769, T3>0.769. Participant characteristics were calculated by Ts of apo B/apo A1. Results were expressed as frequencies and percentages for categorical variables, means and standard deviations (SDs) for normally distributed continuous variables, and medians and interquartile ranges for continuous variables not normally distributed. Chi-squared, one-way ANOVA, or Kruskal–Wallis tests were used to test for differences in categorical or continuous factors among different categories of apo B/apo A1. Survival times were estimated from Kaplan–Meier curves, and differences in survival probabilities among groups were assessed using the log-rank test. The associations between apo B/apo A1 ratio and all-cause mortality and cardiovascular events were examined in Cox proportional hazards models. The censored data included switching to HD, renal transplantation, moving to another center, declining additional treatment, loss to follow-up, or still at our PD center on May 31, 2017. Unadjusted associations were first examined followed by adjustments for age and sex, diabetes and CVD, systolic blood pressure (SBP), body mass index (BMI), total urea clearances (tKt/V) and eGFR, hemoglobin, neutrophil to lymphocyte ratio (N/L), albumin. Next, TG, CHOL as well as lipid lowering agents were added to examine whether apo B/apo A1 ratio was independently associated with mortality and cardiovascular events. Covariates with P < 0.05 in the univariate Cox analyses or thought to be clinical significant were chosen for multivariate Cox proportional hazards regression. The results were expressed as the hazard ratio (HR) and 95% confidence interval (95% CI). All descriptive and multivariate analyses were conducted using SPSS version 22.0 (SPSS, Inc., Chicago, IL). A value of P < 0.05 was considered statistically significant.
Baseline patient characteristics
Apo B/apo A1 tertiles
Baseline characteristics of individuals stratified by tertiles of apo B/apo A1 ratio
Apo B/Apo A1 Ratio Tertiles
≤0.545 (n = 285)
0.545 − 0.769 (n = 285)
>0.769 (n = 290)
50.9 ± 14.8
48.7 ± 14.3
50.0 ± 14.5
49.9 ± 14.5
Body mass index (kg/m2)
21.0 ± 3.2
22.2 ± 3.5
22.6 ± 3.4
21.9 ± 3.4
Systolic pressure (mmHg)
145 ± 27
148 ± 26
147 ± 26
147 ± 26
Diastolic pressure (mmHg)
87 ± 17
90 ± 15
88 ± 15
87 ± 17
2.01 (1.43, 2.53)
2.26 (1.79, 2.69)
2.23 (1.81, 2.80)
2.18 (1.68, 2.70)
eGFR (ml/min per 1.73 m2)
2.66 (1.54, 4.09)
3.59 (2.02, 5.82)
3.85 (1.89, 6.07)
3.26 (1.78, 5.56)
76.65 ± 16.48
79.71 ± 16.19
80.74 ± 16.75
79.04 ± 16.55
3.27 (2.37, 4.75)
3.50 (2.53, 5.53)
3.86 (2.61, 5.20)
3.58 (2.50, 5.12)
35.90 ± 5.00
35.70 ± 5.31
34.50 ± 5.29
35.36 ± 5.23
Total cholesterol (mmol/L)
3.56 (3.05, 4.30)
4.03 (3.46, 4.80)
4.55 (3.84, 5.40)
4.06 (3.34, 4.89)
1.00 (0.73, 1.36)
1.27 (0.91, 1.72)
1.68 (1.14, 2.21)
1.28 (0.89, 1.78)
Low density lipoprotein (mmol/L)
1.90 (1.40, 2.30)
2.31 (1.89, 2.93)
2.81 (2.24, 3.46)
2.30 (1.83, 2.94)
High density lipoprotein (mmol/L)
1.20 (0.96, 1.53)
1.14 (0.92, 1.42)
0.98 (0.81, 1.16)
1.08 (0.89, 1.37)
Apo B (g/L)
0.60 (0.50, 0.70)
0.80 (0.70, 0.90)
1.07 (0.90, 1.41)
0.80 (0.63, 1.00)
Apo A1 (g/L)
1.38 (1.22, 1.59)
1.23 (1.10, 1.40)
1.09 (0.98, 1.23)
1.22 (1.07, 1.41)
Lipoprotein (a) (mg/L)
284 (141, 514)
303 (160, 501)
409 (226, 663)
328 (172, 586)
Lipid-lowering agents use (%)
The correlation of lipid parameters
Correlation between Apo B/Apo A1 and parameters of lipid and inflammation
Apo B/Apo A1
The correlation of Apo B/apo A1, all-cause mortality, and cardiovascular events
The associations of apo A1, apo B, and the apo B/apo A1 ratio (Tertile3 Vs Tertile1) with all-cause mortality and cardiovascular events
Apo B/Apo A1 ratiod
HR (95% CI)
HR (95% CI)
HR (95% CI)
0.64 (0.39 - 1.08)
1.22 (0.78 - 1.90)
1.62 (1.15 - 2.29)
0.47 (0.25 - 0.89)
0.92 (0.52 - 1.65)
1.59 (1.05 - 2.43)
0.48 (0.24 - 0.94)
0.73 (0.31 - 1.72)
1.60 (1.02 - 2.49)
0.47 (0.25 - 0.90)
1.04 (0.60 - 1.80)
1.76 (1.17 - 2.63)
0.39 (0.18 - 0.83)
0.80 (0.40 - 1.61)
1.72 (1.05 - 2.81)
0.44 (0.19 - 1.02)
1.14 (0.42 - 3.10)
2.04 (1.21 - 3.44)
In this retrospective cohort study, we identified the correlation between the serum apo B/apo A1 ratio and PD patient characteristics. We found, for the first time, that a higher apo B/apo A1 ratio is strongly correlated with increased all-cause mortality and cardiovascular events in PD patients. Consistent with the empirical results from HD patients and non-CKD patients [9, 12–15], the apo B/apo A1 ratio can be used as an important risk indicator for clinicians in various fields, including dialysis.
Apo B is a key basal unit of atherogenic lipoprotein including VLDL, IDL, and LDL. Since each of these lipoproteins detects only one apo B molecule, apo B measurements have been used to determine the precise number of the atherogenic lipoproteins in patients . Previous studies indicated that apo B was a strong predictor of mortality and cardiovascular risk [9, 16]. Contrary to these studies, we did not find a significant correlation between apo B and these events. Some differences between these studies and our results are worth noting. First, in our cohort study, the follow-up time was approximately 2 years, whereas other studies have follow-up times of more than 7 years. Second, we enrolled incident PD patients in our study, whereas Sato et al.  assessed the changes apo B in prevalent HD patients. These possibilities may cause the variations between our results and others, and these contradictions should be further elucidated in future studies.
In contrast to apo B, apo A1 is a main constituent of HDL. Although each HDL particle contains five apo A1 molecules, systemic apo A1 levels have been used as an indicator for HDL cholesterol concentrations . The relationship between apo A1 and cardiovascular events remains controversial. A large meta-analysis of prospective studies in the general populations shows an inverse association between apo A1 and incident coronary heart disease . However, Zhu et al.  found that apo A1 was not correlated with cardiovascular events in the general population. In the diabetes dialysis study in German, apo A1 failed to predict cardiovascular events or all-cause mortality . Sato et al.  also found that apo A1 was not independently associated with CVD-related and all-cause mortality. Interesting, in this study, we found that apo A1 had a higher association with the prevention of mortality in adjusted models, and cardiovascular events in model 1 and model 2, with a marginal significance for cardiovascular events in model 3. We speculate that the difference in population and follow-up time may be important factors for apo A1 adjustment and application.
The apo B/apo A1 ratio is a typical marker for the atherogenic /antiatherogenic condition, and a higher apo B/apo A1 ratio represents progression in the atherosclerotic state. Previous studies have suggested that a high apo B/apo A1 ratio strongly correlates with pathophysiological markers of atherosclerosis defined by coronary angiography [8, 20], and calcium scores of the coronary arteries , and by ultrasound techniques such as the thickness of carotid arteries [16, 22, 23], endothelial dysfunction  and existence of femoral plaques . In addition, a high apo B/apo A1 ratio can also be used to predict risk of carotid plaque development  and major adverse cardiovascular events [14, 27–29]. Our findings are in agreement with these studies and show that the apo B/apo A1 ratio is independently associated with cardiovascular events.
Although the apo B/apo A1 ratio is considered as a risk predictor for CVD mortality in the general population [14, 30], to date, few studies have used the apo B/apo A1 ratio to predict the mortality of dialysis patients. The results were also conflicting. For example, Sato et al.  showed that a higher apo B/apo A1 ratio was associated with an increased risk of all-cause and CVD-related mortality in prevalent HD patients. However, in that study, BMI, which has been associated lower mortality risk, was not adjusted. Another study demonstrated that the baseline apo B/apo A1 ratio did not correlate with 4-year mortality . In that study, after adjustment for confounding factors, a higher apo B/apo A1 ratio predicted first-year survival and the next 3 years mortality, and an increased ratio during the first year was also associated with a survival advantage in dialysis patients. However, this association lost significance after adjustment for the protein-energy wasting index. In this study, our findings extended this observation and indicated that the increased risk of all-cause mortality is associated with an increase of the apo B/apo A1 ratio, independent of BMI and N/L, in PD patients. It was reported that the lipid profile was different in PD and HD, and the apo B/apo A1 ratio was higher in patients on HD than patients receiving PD , which is supported by the previous study by Sato et al.  and our results. However, our study indicated that the association between the apo B/apo A1 ratio and mortality in PD patients was similar to the previous study in HD patients .
The present study also has limitations to discuss. First, this is a retrospective study, which can only lead to associations but not causality. Second, the number of patients is relatively small. Third, in this study, we only applied the baseline data but did not exclude patients who had already taken lipid-lowering medications, nor considered the data changes during the follow-up period. Fourth, because of the limited sample size, the potential risk factors were not all adjusted in this cohort study. Hence, the effects of residual confounding factors cannot be eliminated completely. Our future studies will address the improvement of these issues.
In summary, despite conflicting evidence of lipid effects on the prognosis of PD patients, our results found significant associations between the apo B/apo A1 ratio, cardiovascular events, and all-cause mortality in PD patients. The apo B/apo A1 ratio can serve as a risk marker for the risk of the CVDs and mortality in PD patients.
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
XZ conceived the study, YC, CY and SL participated in the design, LD, YY, PQ, DP, BZ collected the data, XZ performed statistical analyses, XZ drafted the manuscript, QC edited and checked the manuscript. All of the authors have read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the ethics committee of The First Affiliated Hospital of Nanchang University. It was conducted according to the standards of the Declaration of Helsinki.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Kaysen GA. Hyperlipidemia of chronic renal failure. Blood Purif. 1994;12:60–7.View ArticlePubMedGoogle Scholar
- Ikewaki K. In vivo kinetic studies to further understand pathogenesis of abnormal lipoprotein metabolism in chronic kidney disease. Clin Exp Nephrol. 2014;18:261–4.View ArticlePubMedGoogle Scholar
- Zhao W, Zheng XL, Jiang ZN, Liao XB, Zhao SP. Risk factors associated with atherogenic dyslipidemia in the presence of optimal statin therapy. Int J Cardiol. 2017;248:355–60.View ArticlePubMedGoogle Scholar
- Quispe R, Manalac RJ, Faridi KF, Blaha MJ, Toth PP, Kulkarni KR, Nasir K, Virani SS, Banach M, Blumenthal RS, Martin SS, Jones SR. Relationship of the triglyceride to high-density lipoprotein cholesterol (TG/HDL-C) ratio to the remainder of the lipid profile: the very large database of Lipids-4 (VLDL-4) study. Atherosclerosis. 2015;242:243–50.View ArticlePubMedGoogle Scholar
- Yusuf S, Hawken S, Ounpuu S, Dans T, Avezum A, Lanas F, McQueen M, Budaj A, Pais P, Varigos J, Lisheng L. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. 2004;364:937–52.View ArticlePubMedGoogle Scholar
- Sniderman AD, Pedersen T, Kjekshus J. Putting low-density lipoproteins at center stage in atherogenesis. Am J Cardiol. 1997;79:64–7.View ArticlePubMedGoogle Scholar
- Andrikoula M, McDowell IF. The contribution of ApoB and ApoA1 measurements to cardiovascular risk assessment. Diabetes Obes Metab. 2008;10:271–8.View ArticlePubMedGoogle Scholar
- Song Y, Yang Y, Zhang J, Wang Y, He W, Zhang X, Zhu J, Lu Z. The apoB100/apoAI ratio is independently associated with the severity of coronary heart disease: a cross sectional study in patients undergoing coronary angiography. Lipids Health Dis. 2015;14:150.View ArticlePubMedPubMed CentralGoogle Scholar
- Sato Y, Fujimoto S, Toida T, Nakagawa H, Yamashita Y, Iwakiri T, Fukuda A, Iwatsubo S. Apoprotein B/Apoprotein a-1 ratio and mortality among prevalent dialysis patients. Clin J Am Soc Nephrol. 2016;11:840–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Samouilidou EC, Karpouza AP, Kostopoulos V, Bakirtzi T, Pantelias K, Petras D, Tzanatou-Exarchou H, GE J. Lipid abnormalities and oxidized LDL in chronic kidney disease patients on hemodialysis and peritoneal dialysis. Ren Fail. 2012;34:160–4.View ArticlePubMedGoogle Scholar
- Wheeler DC, London GM, Parfrey PS, Block GA, Correa-Rotter R, Dehmel B, Drueke TB, Floege J, Kubo Y, Mahaffey KW, Goodman WG, Moe SM, Trotman ML, Abdalla S, Chertow GM, Herzog CA. Effects of cinacalcet on atherosclerotic and nonatherosclerotic cardiovascular events in patients receiving hemodialysis: the EValuation of Cinacalcet HCl therapy to lower CardioVascular events (EVOLVE) trial. J Am Heart Assoc. 2014;3:e1363.View ArticleGoogle Scholar
- Walldius G, Jungner I, Holme I, Aastveit AH, Kolar W, Steiner E. High apolipoprotein B, low apolipoprotein A-I, and improvement in the prediction of fatal myocardial infarction (AMORIS study): a prospective study. Lancet. 2001;358:2026–33.View ArticlePubMedGoogle Scholar
- Dunder K, Lind L, Zethelius B, Berglund L, Lithell H. Evaluation of a scoring scheme, including proinsulin and the apolipoprotein B/apolipoprotein A1 ratio, for the risk of acute coronary events in middle-aged men: Uppsala longitudinal study of adult men (ULSAM). Am Heart J. 2004;148:596–601.View ArticlePubMedGoogle Scholar
- Walldius G, Aastveit AH, Jungner I. Stroke mortality and the apoB/apoA-I ratio: results of the AMORIS prospective study. J Intern Med. 2006;259:259–66.View ArticlePubMedGoogle Scholar
- Walldius G, Jungner I. The apoB/apoA-I ratio: a strong, new risk factor for cardiovascular disease and a target for lipid-lowering therapy--a review of the evidence. J Intern Med. 2006;259:493–519.View ArticlePubMedGoogle Scholar
- Zhu YM, Verma S, Fung M, McQueen MJ, Anderson TJ, Lonn EM. Association of apolipoproteins b and a-1 with markers of vascular health or cardiovascular events. Can J Cardiol. 2017;33:1305–11.View ArticlePubMedGoogle Scholar
- Catapano AL, Graham I, De Backer G, Wiklund O, Chapman MJ, Drexel H, Hoes AW, Jennings CS, Landmesser U, Pedersen TR, Reiner Z, Riccardi G, Taskinen MR, Tokgozoglu L, Verschuren WM, Vlachopoulos C, Wood DA, Zamorano JL. 2016 ESC/EAS guidelines for the Management of Dyslipidaemias. Eur Heart J. 2016;37:2999–3058.View ArticlePubMedGoogle Scholar
- Thompson A, Danesh J. Associations between apolipoprotein B, apolipoprotein AI, the apolipoprotein B/AI ratio and coronary heart disease: a literature-based meta-analysis of prospective studies. J Intern Med. 2006;259:481–92.View ArticlePubMedGoogle Scholar
- Silbernagel G, Genser B, Drechsler C, Scharnagl H, Grammer TB, Stojakovic T, Krane V, Ritz E, Wanner C, Marz W. HDL cholesterol, apolipoproteins, and cardiovascular risk in hemodialysis patients. J Am Soc Nephrol. 2015;26:484–92.View ArticlePubMedGoogle Scholar
- Liting P, Guoping L, Zhenyue C. Apolipoprotein B/apolipoprotein A1 ratio and non-high-density lipoprotein cholesterol. Predictive value for CHD severity and prognostic utility in CHD patients. Herz. 2015;40(Suppl 1):1–7.View ArticlePubMedGoogle Scholar
- Simon A, Chironi G, Gariepy J, Del PM, Levenson J. Differences between markers of atherogenic lipoproteins in predicting high cardiovascular risk and subclinical atherosclerosis in asymptomatic men. Atherosclerosis. 2005;179:339–44.View ArticlePubMedGoogle Scholar
- Huang F, Yang Z, Xu B, Bi Y, Xu M, Xu Y, Lu J, Liu Y, Dai M, Zhou W, Wang W, Chen Y. Both serum apolipoprotein B and the apolipoprotein B/apolipoprotein A-I ratio are associated with carotid intima-media thickness. PLoS One. 2013;8:e54628.View ArticlePubMedPubMed CentralGoogle Scholar
- Dahlen EM, Lanne T, Engvall J, Lindstrom T, Grodzinsky E, Nystrom FH, Ostgren CJ. Carotid intima-media thickness and apolipoprotein B/apolipoprotein A-I ratio in middle-aged patients with type 2 diabetes. Diabet Med. 2009;26:384–90.View ArticlePubMedGoogle Scholar
- Emoto T, Sawada T, Morimoto N, Tenjin T, Wakimoto T, Ikeda F, Sato C, Terashita D, Mizoguchi T, Mizuguchi T, Okamoto H, Matsuo Y, Kim SK, Takarada A, Yokoyama M. The apolipoprotein B/A1 ratio is associated with reactive oxygen metabolites and endothelial dysfunction in statin-treated patients with coronary artery disease. J Atheroscler Thromb. 2013;20:623–9.View ArticlePubMedGoogle Scholar
- Schmidt C, Fagerberg B. ApoB/apoA-I ratio is related to femoral artery plaques in 64-year-old women also in cases with low LDL cholesterol. Atherosclerosis. 2008;196:817–22.View ArticlePubMedGoogle Scholar
- Steffen BT, Guan W, Remaley AT, Stein JH, Tattersall MC, Kaufman J, Tsai MY. Apolipoprotein B is associated with carotid atherosclerosis progression independent of individual cholesterol measures in a 9-year prospective study of multi-ethnic study of atherosclerosis participants. J Clin Lipidol. 2017;11:1181–91.View ArticlePubMedGoogle Scholar
- van der Steeg WA, Boekholdt SM, Stein EA, El-Harchaoui K, Stroes ES, Sandhu MS, Wareham NJ, Jukema JW, Luben R, Zwinderman AH, Kastelein JJ, Khaw KT. Role of the apolipoprotein B-apolipoprotein A-I ratio in cardiovascular risk assessment: a case-control analysis in EPIC-Norfolk. Ann Intern Med. 2007;146:640–8.View ArticlePubMedGoogle Scholar
- Albers JJ, Slee A, O'Brien KD, Robinson JG, Kashyap ML, Kwiterovich PJ, Xu P, Marcovina SM. Relationship of apolipoproteins A-1 and B, and lipoprotein(a) to cardiovascular outcomes: the AIM-HIGH trial (Atherothrombosis intervention in metabolic syndrome with low HDL/high triglyceride and impact on Global Health outcomes). J Am Coll Cardiol. 2013;62:1575–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Kappelle PJ, Gansevoort RT, Hillege JL, Wolffenbuttel BH, Dullaart RP. Apolipoprotein B/A-I and total cholesterol/high-density lipoprotein cholesterol ratios both predict cardiovascular events in the general population independently of nonlipid risk factors, albuminuria and C-reactive protein. J Intern Med. 2011;269:232–42.View ArticlePubMedGoogle Scholar
- Sierra-Johnson J, Fisher RM, Romero-Corral A, Somers VK, Lopez-Jimenez F, Ohrvik J, Walldius G, Hellenius ML, Hamsten A. Concentration of apolipoprotein B is comparable with the apolipoprotein B/apolipoprotein A-I ratio and better than routine clinical lipid measurements in predicting coronary heart disease mortality: findings from a multi-ethnic US population. Eur Heart J. 2009;30:710–7.View ArticlePubMedGoogle Scholar
- Chmielewski M, Carrero JJ, Qureshi AR, Axelsson J, Heimburger O, Berglund L, Barany P, Rutkowski B, Lindholm B, Stenvinkel P. Temporal discrepancies in the association between the apoB/apoA-I ratio and mortality in incident dialysis patients. J Intern Med. 2009;265:708–16.View ArticlePubMedGoogle Scholar
- Liu J, Rosner MH. Lipid abnormalities associated with end-stage renal disease. Semin Dial. 2006;19:32–40.View ArticlePubMedGoogle Scholar