Atherosclerotic vascular disease is more prevalent among black ESKD patients on long-term CAPD in South Africa.
Adult
Atherosclerosis
/ blood
Black People
/ statistics & numerical data
Carotid Intima-Media Thickness
Case-Control Studies
Cross-Sectional Studies
Echocardiography
Female
Humans
Hypertrophy, Left Ventricular
/ diagnostic imaging
Kidney Failure, Chronic
/ blood
Male
Middle Aged
Peritoneal Dialysis, Continuous Ambulatory
/ adverse effects
Prevalence
Renal Dialysis
/ adverse effects
Renal Insufficiency, Chronic
/ blood
South Africa
/ epidemiology
Atherosclerotic vascular disease
Chronic kidney disease
Continous ambulatory peritoneal dialysis
End-stage kidney disease
Haemodialysis
Left ventricular hypertrophy
Journal
BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793
Informations de publication
Date de publication:
30 10 2019
30 10 2019
Historique:
received:
13
02
2018
accepted:
09
10
2019
entrez:
1
11
2019
pubmed:
2
11
2019
medline:
22
10
2020
Statut:
epublish
Résumé
Occurrence of cardiovascular disease (CVD) in the setting of chronic kidney disease (CKD) can be described as a "cruel alliance", with CVD responsible for about half of all deaths among CKD patients. Chronic kidney disease patients are more likely to die from CVD than progress to end stage kidney disease (ESKD). Dyslipidaemia, a known traditional risk factor for CVD, is highly prevalent among CKD patients and with an even higher frequency among ESKD patients on dialytic therapies. Prolonged exposure of continuous ambulatory peritoneal dialysis (CAPD) patients to high glucose concentrations in CAPD fluid have been associated with increased risk of cardiovascular events. In this study, we investigated the relationship of atherosclerotic vascular disease (AsVD) to clinical and echocardiographic parameters among black South Africans with CKD (stage 3) and ESKD on CAPD and haemodialysis (HD). This was a cross-sectional study of 40 adult (18-65 years) non-diabetic CKD patients (kidney disease outcome quality initiative [KDOQI] stage 3), 40 ESKD patients on CAPD, 40 ESKD patients on HD and 41 age and sex-matched healthy controls. An interviewer-administered questionnaire was used to obtain information on participants' sociodemographic and cardiovascular risk factors. Anthropometric parameters were measured. Serum blood samples were analysed for creatinine, albumin and lipid profile; lipoprotein ratios, Framingham's risk score and the 10-year risk of developing coronary heart disease (CHD) were calculated. Echocardiography was performed on all patients and carotid intima media thickness (CIMT) was measured in both right and left carotid arteries at 1 cm proximal to the carotid bulb. Spearman's rank correlation and binary logistic regression were conducted to determine the relationship of AsVD to clinical and echocardiographic parameters. Atherosclerotic vascular disease was most prevalent among ESKD patients on CAPD (70%, n = 28/40). Chronic kidney disease and HD patients exhibited a similar prevalence (47.5%, n = 19/40), while the prevalence in controls was 17.1% (n = 7/41). Presence of AsVD was associated with significantly older age, higher waist hip ratio (WHR), left ventricular mass index (LVMI) and Framingham's 10-year risk of developing CHD. Significant differences in clinical and echocardiographic parameters were observed when the study groups were compared. Age and LVH independently predicted AsVD. Atherosclerotic vascular disease was more prevalent among CAPD patients compared to pre-dialysis CKD and HD patients. Among all lipoprotein ratios assessed, non-HDL-C showed the most consistent significant difference between the groups. Age (> 40 years) and presence of LVH were independent predictors of AsVD.
Sections du résumé
BACKGROUND
Occurrence of cardiovascular disease (CVD) in the setting of chronic kidney disease (CKD) can be described as a "cruel alliance", with CVD responsible for about half of all deaths among CKD patients. Chronic kidney disease patients are more likely to die from CVD than progress to end stage kidney disease (ESKD). Dyslipidaemia, a known traditional risk factor for CVD, is highly prevalent among CKD patients and with an even higher frequency among ESKD patients on dialytic therapies. Prolonged exposure of continuous ambulatory peritoneal dialysis (CAPD) patients to high glucose concentrations in CAPD fluid have been associated with increased risk of cardiovascular events. In this study, we investigated the relationship of atherosclerotic vascular disease (AsVD) to clinical and echocardiographic parameters among black South Africans with CKD (stage 3) and ESKD on CAPD and haemodialysis (HD).
METHODS
This was a cross-sectional study of 40 adult (18-65 years) non-diabetic CKD patients (kidney disease outcome quality initiative [KDOQI] stage 3), 40 ESKD patients on CAPD, 40 ESKD patients on HD and 41 age and sex-matched healthy controls. An interviewer-administered questionnaire was used to obtain information on participants' sociodemographic and cardiovascular risk factors. Anthropometric parameters were measured. Serum blood samples were analysed for creatinine, albumin and lipid profile; lipoprotein ratios, Framingham's risk score and the 10-year risk of developing coronary heart disease (CHD) were calculated. Echocardiography was performed on all patients and carotid intima media thickness (CIMT) was measured in both right and left carotid arteries at 1 cm proximal to the carotid bulb. Spearman's rank correlation and binary logistic regression were conducted to determine the relationship of AsVD to clinical and echocardiographic parameters.
RESULTS
Atherosclerotic vascular disease was most prevalent among ESKD patients on CAPD (70%, n = 28/40). Chronic kidney disease and HD patients exhibited a similar prevalence (47.5%, n = 19/40), while the prevalence in controls was 17.1% (n = 7/41). Presence of AsVD was associated with significantly older age, higher waist hip ratio (WHR), left ventricular mass index (LVMI) and Framingham's 10-year risk of developing CHD. Significant differences in clinical and echocardiographic parameters were observed when the study groups were compared. Age and LVH independently predicted AsVD.
CONCLUSION
Atherosclerotic vascular disease was more prevalent among CAPD patients compared to pre-dialysis CKD and HD patients. Among all lipoprotein ratios assessed, non-HDL-C showed the most consistent significant difference between the groups. Age (> 40 years) and presence of LVH were independent predictors of AsVD.
Identifiants
pubmed: 31666030
doi: 10.1186/s12882-019-1583-8
pii: 10.1186/s12882-019-1583-8
pmc: PMC6821013
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
399Références
Kidney Int Suppl. 2003 Nov;(87):S24-31
pubmed: 14531770
J Am Coll Cardiol. 2007 Jul 17;50(3):217-24
pubmed: 17631213
J Clin Invest. 1985 Mar;75(3):809-17
pubmed: 3884667
Clin J Am Soc Nephrol. 2009 Aug;4(8):1302-11
pubmed: 19541818
Arch Intern Med. 2004 May 10;164(9):969-76
pubmed: 15136305
Nephrol Dial Transplant. 2008 Jan;23(1):65-71
pubmed: 17965436
Am J Kidney Dis. 2005 Sep;46(3):512-9
pubmed: 16129214
N Engl J Med. 1990 May 31;322(22):1561-6
pubmed: 2139921
Medicine (Baltimore). 2017 Sep;96(37):e8058
pubmed: 28906400
Arch Intern Med. 2006 Sep 25;166(17):1884-91
pubmed: 17000946
Metabolism. 1995 Feb;44(2):228-33
pubmed: 7869920
Perit Dial Int. 2006 Sep-Oct;26(5):523-39
pubmed: 16973506
J Am Heart Assoc. 2017 Sep 22;6(9):null
pubmed: 28939714
Arq Bras Cardiol. 2014 May;102(5):473-80
pubmed: 24759948
Curr Opin Nephrol Hypertens. 2014 Nov;23(6):578-85
pubmed: 25295959
Ann Afr Med. 2017 Oct-Dec;16(4):192-195
pubmed: 29063904
Hemodial Int. 2012 Jan;16(1):59-68
pubmed: 22099423
Nephrol Dial Transplant. 2010 May;25(5):1474-8
pubmed: 19945955
Ann Intern Med. 2012 Jun 5;156(11):785-95, W-270, W-271, W-272, W-273, W-274, W-275, W-276, W-277,
pubmed: 22312131
J Am Soc Echocardiogr. 2005 Dec;18(12):1440-63
pubmed: 16376782
S Afr Med J. 2007 Apr;97(4):285-8
pubmed: 17446954
Handb Exp Pharmacol. 2015;224:423-53
pubmed: 25522997
Drugs. 1986;31 Suppl 4:192-201
pubmed: 2942387
N Engl J Med. 1974 Mar 28;290(13):697-701
pubmed: 4813742
PLoS One. 2016 Jun 14;11(6):e0156642
pubmed: 27300372
Pan Afr Med J. 2014 Jan 07;17:3
pubmed: 25184020
Am J Nephrol. 2012;36(4):342-7
pubmed: 23107930
Stroke. 2004 Dec;35(12):2782-7
pubmed: 15514185
Nephrology (Carlton). 2012 Sep;17(7):607-15
pubmed: 22515484
N Engl J Med. 1987 Oct 22;317(17):1098
pubmed: 3657876
S Afr Med J. 2007 Aug;97(8 Pt 2):708-15
pubmed: 17952228
Nephrol Dial Transplant. 2003 May;18(5):977-82
pubmed: 12686674
Perit Dial Int. 2007 Jun;27 Suppl 2:S82-6
pubmed: 17556336
Am J Cardiol. 1987 May 29;59(14):91G-94G
pubmed: 3591674
Am J Kidney Dis. 2002 Feb;39(2 Suppl 1):S1-266
pubmed: 11904577
Circulation. 1997 Sep 2;96(5):1432-7
pubmed: 9315528
Clin Sci (Lond). 1997 Dec;93(6):519-25
pubmed: 9497788
Saudi J Kidney Dis Transpl. 2017 Jul-Aug;28(4):818-829
pubmed: 28748884
Perit Dial Int. 2002 Mar-Apr;22(2):220-8
pubmed: 11990407
Nutr Metab Cardiovasc Dis. 2014 Sep;24(9):1035-42
pubmed: 24880738