Clinical Efficacy of Budesonide Enteric-Coated Capsules in the Treatment of IgA nephropathy with subclassication of focal segmental glomerulosclerosis and Analysis of Influencing Factors

 

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https://storage.unitedwebnetwork.com/files/1099/ef6728d15a957d42196b1358ffe47120.pdf
Clinical Efficacy of Budesonide Enteric-Coated Capsules in the Treatment of IgA nephropathy with subclassication of focal segmental glomerulosclerosis and Analysis of Influencing Factors

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Shu
Rong
Shu Rong jingweisy@126.com Shanghai general hospital Nephrology Shanghai China *
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To investigate the clinical efficacy of budesonide enteric-coated capsules (trade name: Naifukang) in patients with subclassication of focal segmental glomerulosclerosis of immunoglobulin A nephropathy (IgAN), and to analyze the impacts of baseline renal function, pathological features, and comorbid metabolic diseases on therapeutic outcomes, so as to provide evidence for individualized treatment.

A retrospective analysis was performed on the clinical data of 22 IgAN patients with subclassication of focal segmental glomerulosclerosis who received Naifukang treatment from October 2024 to September 2025. Data collected included demographic characteristics, baseline comorbidities, pathological parameters, Naifukang administration regimens, and key laboratory indicators before and after treatment, such as 24-hour urinary protein excretion (24h UPE), serum creatinine (Scr), and estimated glomerular filtration rate (eGFR). Descriptive analysis and intergroup comparison were employed to assess differences in therapeutic efficacy.

Among the 22 patients, 14 were male (63.6%), and middle-aged patients (31-45 years) accounted for 68.2%. The proportions of patients with hypertension, hyperlipidemia, and hyperuricemia were 59.1%, 63.6%, and 59.1%, respectively. After treatment, 63.6% of patients achieved a ≥30% reduction in 24h UPE compared with baseline, and 68.2% of patients had an eGFR fluctuation of <5 ml/min/1.73m². The proteinuria improvement rate in the group with baseline eGFR ≥40 ml/min/1.73m² (78.9%) was significantly higher than that in the group with eGFR <40 ml/min/1.73m² (33.3%) (P<0.05). Following comprehensive management, there was no significant difference in therapeutic efficacy between patients with 3 comorbid metabolic diseases and those without (P>0.05).(Tab. 1, Fig. 1)

Tab. 1 Treatment effect

Group

n

≥30% reduction in 24h UPE (n, %)

eGFR fluctuation of <5 ml/min (n, %)

P Value

Overall Efficacy

All Patients

22

14 (63.6%)

15 (68.2%)

-

By Baseline Renal Function

Baseline eGFR ≥ 40

19

15 (78.9%)

14 (73.7%)

P=0.027

 

Baseline eGFR < 40

3

1 (33.3%)

1 (33.3%)

 

By Metabolic Disease

Combined with Metabolic Diseases)

13

8 (61.5%)

10 (76.9%)

P0.05

 

Combined without Metabolic Disease)

9

6 (66.7%)

6 (66.7%)

Fig. 1  Subgroup efficacy comparison

Budesonide enteric-coated capsules exhibit definite overall efficacy in the treatment of IgAN with subclassication of focal segmental glomerulosclerosis, and patients with better baseline renal function gain more significant benefits. High-risk patients with renal insufficiency require combined intensive therapy, and synchronous control of metabolic parameters can ensure therapeutic efficacy in patients with comorbid metabolic diseases.

Kewords