Key result
Microalbuminuria is linked to ~16 g/m² higher LVMI in hypertensive patients.
Why the study?
Microalbuminuria reflects generalized vascular damage in essential hypertension and may predict subclinical cardiac, vascular, and retinal involvement before overt clinical complications arise. This study evaluated its prevalence and association with subclinical target-organ damage.
Is microalbuminuria associated with increased subclinical cardiac, vascular, renal, and retinal target-organ damage in adult patients with essential hypertension?
Cross-Sectional (n=140)
No
Is microalbuminuria associated with increased subclinical cardiac, vascular, renal, and retinal target-organ damage in adult patients with essential hypertension?
Microalbuminuria is present in 43.6% of patients with essential hypertension and is strongly associated with subclinical cardiac, vascular, renal, and retinal target-organ damage, supporting its routine use for risk stratification.
Microalbuminuria may mark higher-risk hypertensive patients with subclinical damage; leaves open its incremental value for screening or risk stratification in prospective studies.
Background: Microalbuminuria (MAU) is a well-established marker of endothelial dysfunction and early renal injury in essential hypertension.It reflects generalized vascular damage and may predict subclinical cardiac, vascular, and retinal involvement even before overt clinical complications arise.Objectives: To evaluate the prevalence of microalbuminuria in essential hypertension and its association with subclinical target-organ damage involving the heart, kidneys, vasculature, and retina.Methods: A hospital-based cross-sectional study was conducted among 140 adult patients with essential hypertension.Demographic, clinical, and biochemical data were collected.Microalbuminuria was measured using the urinary albumin-to-creatinine ratio (UACR, 30-300 mg/g).Echocardiography was performed to determine the left ventricular mass index (LVMI), carotid intima-media thickness (CIMT) was assessed by B-mode ultrasonography, and fundoscopic examination was used to grade hypertensive retinopathy.Patients were classified by hypertension severity and blood-pressure control status.Statistical analysis included t-tests, chi-square tests, and Pearson/Spearman correlations; p < 0.05 was considered significant.Results: Microalbuminuria was present in 43.6% of hypertensive subjects.Compared to those without MAU, affected patients were older (58.4 ± 9.7 vs 54.9 ± 9.1 years; p = 0.031), had higher LVMI (118.7 ± 21.5 vs 102.3 ± 18.9 g/m²; p < 0.0001), greater CIMT (0.86 ± 0.13 vs 0.78 ± 0.12 mm; p = 0.0003), and lower eGFR (74.1 ± 16.8 vs 82.7 ± 17.2 mL/min/1.73m²; p = 0.0035).The prevalence of LVH, elevated CIMT, and hypertensive retinopathy was also significantly higher in the microalbuminuric group (all p < 0.01).UACR correlated positively with LVMI (r = 0.38), CIMT (r = 0.34), and retinopathy grade (ρ = 0.29), and negatively with eGFR (r = -0.41).Microalbuminuria prevalence and severity rose steadily with increasing hypertension stage and poor BP control.Conclusion: Microalbuminuria is highly prevalent in essential hypertension and closely linked with subclinical multi-organ damage.Its presence identifies patients at higher cardiovascular and renal risk who warrant intensified blood-pressure management and follow-up.
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A 2026 study conducted a cross-sectional in Essential hypertension (n=140). Microalbuminuria (UACR 30-300 mg/g) vs. Normoalbuminuria (microalbuminuria absent) was evaluated on Left ventricular mass index (LVMI, g/m²) (MD 16.4 g/m², 95% CI 9.58 to 23.22, p=<0.0001). Microalbuminuria (present in 43.6% of hypertensive patients) was associated with significantly higher left ventricular mass index (118.7 vs 102.3 g/m²; MD 16.4 g/m², p<0.0001) and multi-organ damage.
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