Evidence map›Paper›PMID 40594210›Full record

Trial reportScientific reports2025

Effect of oral sodium bicarbonate supplementation on urine TGF-𝜷 in normal serum bicarbonate CKD, a randomized controlled trial.

Nipon Ngupis, Bancha Satirapoj, Theerasak Tangwonglert, Ouppatham Supasyndh, Paramat Thimachai, Narongrit Siriwattanasit

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Nipon NgupisDivision of Nephrology, Department of Medicine, Phramongkutklao Hospital, College of Medicine, Bangkok, 10400, Thailand.
Bancha SatirapojDivision of Nephrology, Department of Medicine, Phramongkutklao Hospital, College of Medicine, Bangkok, 10400, Thailand.
Theerasak TangwonglertDivision of Nephrology, Department of Medicine, Phramongkutklao Hospital, College of Medicine, Bangkok, 10400, Thailand.
Ouppatham SupasyndhDivision of Nephrology, Department of Medicine, Phramongkutklao Hospital, College of Medicine, Bangkok, 10400, Thailand.
Paramat ThimachaiDivision of Nephrology, Department of Medicine, Phramongkutklao Hospital, College of Medicine, Bangkok, 10400, Thailand.
Narongrit SiriwattanasitDivision of Nephrology, Department of Medicine, Phramongkutklao Hospital, College of Medicine, Bangkok, 10400, Thailand. nsiriwattanasit@gmail.com.ORCID http://orcid.org/0009-0001-8412-4021

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The consequences of chronic subclinical metabolic acidosis, characterized by an increase in single nephron ammonium generation, contribute to the progression of chronic kidney disease (CKD). Therefore, sodium bicarbonate (NaHCO₃) supplementation in CKD with normal serum bicarbonate patients may reduce kidney fibrosis and slow CKD progression. This study aimed to evaluate the impact of high-dose NaHCO₃ supplementation on urinary transforming growth factor-beta (TGF-β), a biomarker of kidney fibrosis, in non-diabetic CKD patients with normal serum bicarbonate levels. We conducted a single-center, randomized, open-label controlled trial in patients with non-diabetic CKD stage 3-4 and normal serum bicarbonate (22-26 mEq/L). Participants were randomized to receive high-dose NaHCO₃ (0.8 mEq/kg/day) or standard care for 12 weeks. The primary outcome was the change in urinary TGF-β-to-creatinine ratio from baseline. Secondary outcomes included changes in urinary albumin-to-creatinine ratio (UACR), urine pH, serum electrolytes, blood pressure, and adverse events. A total of 64 participants were randomized (NaHCO₃ group: n = 32; control group: n = 32). There was no significant difference in the percentage change of urinary TGF-β (NaHCO₃: -1.86% vs. control: 5.75%; p = 0.477). However, the NaHCO₃ group demonstrated a significant increase in urine pH mean difference (0.56; 95% CI: 0.3,0.82 vs. 0,95% CI -0.24,0.24; p = 0.002) compared to the control group. Similarly, no significant differences were observed in UACR, serum electrolytes, blood pressure, or body weight between groups. No serious adverse events were reported. High-dose NaHCO₃ supplementation in non-diabetic CKD patients with normal serum bicarbonate levels did not significantly reduce urinary TGF-β over 12 weeks but effectively increased urine pH without adverse effects. These findings suggest that NaHCO₃ is safe; however, its role in modulating profibrotic biomarkers in CKD requires further investigation. Longer-term studies and alternative alkali therapies should be explored to determine the optimal strategies for preserving kidney function in this population.Clinical trial registration: TCTR20240817007 (17/08/2024).

Indexed as

BicarbonatesRenal Insufficiency, ChronicSodium BicarbonateTransforming Growth Factor betaAdministration, OralAdultAgedBiomarkersCreatinineDietary SupplementsFemaleHumansMaleMiddle AgedBicarbonatesBiomarkersCreatinineSodium BicarbonateTransforming Growth Factor betaChronic kidney diseaseSubclinical metabolic acidosisUrinary TGF-β

Identifiers

PMID40594210
PMCPMC12215713

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.