Evolution of Left Ventricular Hypertrophy After Stabilisation of Chronic Kidney Disease: Results of a Prospective Study

Authors

Amine Zineb

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Moufid Omar

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Rouiyess Dounia

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Bouziane Maha

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Haboub Meryem

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Arous Salim

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Med el Ghali Bennouna

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

Drighil Abdenasser

Cardiology Department, Ibn Rochd Hospital, Casablanca (Morocco)

A.Karaky

Cardioloy Department, Saint-Raphael –Frejus Intercommunal Hospital Center (Morocco)

D.Yomi

Cardioloy Department, Saint-Raphael –Frejus Intercommunal Hospital Center (Morocco)

I.Kotirkow

Cardioloy Department, Saint-Raphael –Frejus Intercommunal Hospital Center (Morocco)

Article Information

DOI: 10.51244/IJRSI.2025.120800137

Subject Category: Public Health

Volume/Issue: 12/8 | Page No: 1569-1574

Publication Timeline

Submitted: 2025-08-05

Accepted: 2025-08-13

Published: 2025-09-15

Abstract

Background: Left ventricular hypertrophy (LVH) is a common and serious cardiovascular complication in patients with chronic kidney disease (CKD), contributing significantly to morbidity and mortality. Whether LVH can regress after stabilisation of CKD remains a key clinical question.
Objective: To evaluate the regression of LVH after one year of optimised treatment aimed at stabilising renal function and controlling cardiovascular risk factors in patients with CKD stages 3 to 5.
Methods: A prospective study included 40 patients (30–75 years old) with CKD stages 3–5 and echocardiographic LVH. Patients received optimised management over 12 months, including tight blood pressure control (<130/80 mmHg), correction of anaemia, and management of phosphocalcium metabolism. Echocardiographic measurements of left ventricular mass index (LVMI) were compared at baseline and after 12 months.
Results: After 12 months, 70% of patients showed regression of LVH, with complete normalisation in 25% and partial reduction in 45%. Regression was associated with optimal blood pressure control (p<0.01), effective correction of anaemia (p<0.05), and treatment of phosphocalcium disorders (p<0.05). Conversely, persistent LVH (30%) was linked to advanced myocardial fibrosis, rapid CKD progression (GFR <15 ml/min), and poor treatment adherence. LVH regression was accompanied by improved diastolic function, reduced NT-proBNP levels, fewer heart failure symptoms, and a 40% decrease in hospitalisations for cardiac decompensation.

Keywords

Left ,Ventricular ,Hypertrophy, Stabilisation ,Chronic Kidney Disease

Downloads

References

1. London GM, Marchais SJ, Guerin AP, et al (2001). Cardiovascular disease in chronic renal failure: Pathophysiologic aspects. Journal of the American Society of Nephrology, 12(2), 473-481.
→ Describes the impact of CKD on cardiac structure, including the development of LVH. [Google Scholar] [Crossref]

2. Mizuno M, Shimizu M, Matsumoto Y, et al. (2018). Regression of left ventricular hypertrophy after strict blood pressure control in patients with chronic kidney disease. Hypertension Research, 41(8), 650-658.
→ Confirms that optimised management of hypertension in patients with CKD promotes regression of LVH. [Google Scholar] [Crossref]

3. Wright JT Jr, Bakris G, Greene T, et al (2002). Effect of blood pressure lowering and antihypertensive drug class on progression of hypertensive kidney disease: Results from the AASK trial. JAMA, 288(19), 2421-2431.
→ Highlights the effect of RAAS inhibitors on the regression of LVH. [Google Scholar] [Crossref]

4. Singh AK, Szczech L, Tang KL, et al (2006). Correction of anemia with epoetin alfa in chronic kidney disease. New England Journal of Medicine, 355(20), 2085-2098.
→ Shows the impact of correction of anemia on LVH and cardiac function. [Google Scholar] [Crossref]

5. Drüeke TB, Locatelli F, Clyne N, et al (2006). Normalization of hemoglobin level in patients with chronic kidney disease and anemia. New England Journal of Medicine, 355(20), 2071-2084.
→ Confirms that optimisation of phosphocalcium metabolism and anaemia reduces ventricular remodelling. [Google Scholar] [Crossref]

6. Querejeta R, Varo N, López B, et al. (2004). Serum carboxy-terminal propeptide of procollagen type I is a marker of myocardial fibrosis in hypertensive patients. Circulation, 110(7), 812-817.
→ Demonstrates that myocardial fibrosis limits the reversibility of LVH. [Google Scholar] [Crossref]

7. Briet M, Bozec E, Laurent S, et al. (2012). Arterial stiffness and pulse pressure amplification in chronic kidney disease patients. Hypertension, 60(1), 145-150.
→ Describes the association between CKD progression, arterial stiffness and LVH. [Google Scholar] [Crossref]

8. Dahlof B, Pennert K, Hansson L. (2002). Reversal of left ventricular hypertrophy in hypertensive patients: A meta-analysis of 109 treatment studies. American Journal of Hypertension, 15(8), 692-700.
→ Shows the impact of LVH regression on cardiovascular mortality and quality of life. [Google Scholar] [Crossref]

9. Heerspink HJ, Perkovic V, Jardine MJ, et al. (2020). Canagliflozin and renal outcomes in type 2 diabetes and nephropathy. New England Journal of Medicine, 380(24), 2295-2306 [Google Scholar] [Crossref]

Metrics

Views & Downloads

Similar Articles