D-Mannose for Kidney Disease

Verdict: No evidence for kidney disease

No clinical studies have tested oral D-mannose supplements as a treatment for kidney disease, so its benefit cannot be claimed. The grade reflects an absence of relevant evidence, not proof that it works or that it has been disproven for this use.

U ⚫ U Unverified Insufficient Evidence

🔬Why this grade7-layer evidence engine

This pairing earns an Unverified grade because no trial has ever measured oral D-mannose against any kidney-disease outcome (eGFR, proteinuria, CKD progression, or acute kidney injury). The only randomized data, the Manotras pilot in 60 kidney-transplant recipients (PMID 38637262), tested D-mannose plus proanthocyanidins for urinary tract infection prophylaxis, found no benefit, and reported no kidney-function endpoints.

The wider D-mannose trial base targets UTIs, not the kidneys: a 2025 meta-analysis of six RCTs (PMID 41004704, n=1167) found it did not reduce recurrent UTIs versus control or antibiotics. The one paper directly linking mannose to the kidney is a Mendelian randomization analysis (PMID 38354117) suggesting higher endogenous serum mannose is associated with worse CKD outcomes. That signal points opposite to the consumer hope of kidney protection, but it concerns the body's own metabolite, not a swallowed supplement, so it neither proves harm nor disproves a benefit.

Authoritative bodies are silent on this specific use. FDA action and an EFSA rejection both concern UTI claims, NHS frames D-mannose as a non-prescription sugar rather than a medicine, and the NIH ODS, Mayo Clinic, Cleveland Clinic, Harvard Health, and kidney specialty societies do not address it for kidney disease. Because D-mannose is cleared by the kidneys, several sources advise people with reduced kidney function to consult a clinician before use, but this is precautionary opinion, not trial evidence.

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Scoring transparency

All scores computed by a 7-layer evidence engine — fully auditable
Raw score 0.44
D
C
B
A
S
← counter-evidence / ineffectiveeffective / strong evidence →
Final grade
U · Insufficient Evidence
Confidence
71%
Broadly consistent
Evidence level
E3
Single high-quality meta-analysis

How strongly each layer supports this effect

lower = less supportive
L11 AI re-checkIndependent read
0.20
L2 PubMedPrimary literature
0.45
L3 MechanismPlausibility
0.45
L1 ExamineGlobal benchmark
0.50
L5 Clinical bodiesAuthoritative stance
0.50
Against Mixed Supports
View the full decision path (audit trail)
  1. compute_raw_score — 加權公式: L2×0.30 + L3×0.25 + L5×0.25 + L11×0.10 + L1×0.10 = 0.443
  2. tier_from_score — 依分數區間映射至 tier letter
  3. apply_hec_rules — 高階證據未達主導 (0 positive vs 1 negative),由 raw_score 決定
  4. tier_strict_requirement_check — | C→U 因 scope.conflation_risk=true 且 L11 獨評較低 (B7-2 tier cap)
  5. detect_disputes — 偵測到 0 個 hard + 0 個 soft dispute
  6. decide_status — 依 tier + dispute 結果決定 status

📄PubMed studies (3)L2 · primary research & systematic reviews

Randomized clinical trial of non-antibiotic prophylaxis with d-Mannose plus Proanthocyanidins vs. Proanthocyanidins alone for urinary tract infections and asymptomatic bacteriuria in de novo kidney…
PMID: 38637262 2024 RCT (double-blind) n = 60
Finding: 「the use of d-Mannose plus PAC does not seem capable to prevent it」— D-mannose + PAC did NOT reduce UTI vs PAC alone (cystitis 7% vs 4%; pyelonephritis 4% vs 5%; asymptomatic bacteriuria 17% vs 14%). No renal function outcomes reported.
🟠 Limited quality Effect size: No significant difference; small pilot
View on PubMed
Mannose and glycine: Metabolites with potentially causal implications in chronic kidney disease pathogenesis
PMID: 38354117 2024 Other
Finding: Serum mannose levels showed putatively causal associations with CKD, eGFR (creatinine-based), microalbuminuria, and UACR after Bonferroni correction. Authors describe mannose as a potential biomarker / therapeutic target for CKD — direction of effect indicates higher endogenous mannose linked to worse CKD outcomes. Does NOT evaluate oral D-mannose supplementation.
Effect size: Causal estimate via MR; effect size not directly interpretable as supplement dose-response
View on PubMed
Efficacy of D-mannose as prophylaxis of recurrent urinary tract infection: a systematic review and meta-analysis of randomized controlled trials
PMID: 41004704 2025 統合分析 n = 1,167
Finding: 「D-mannose did not reduce the incidence of recurrent UTIs compared with control or antibiotics in high-risk patients」(RR 0.57, 95% CI 0.29–1.15 vs control; RR 0.39, 95% CI 0.12–1.25 vs antibiotics). Included one kidney-transplant trial but analysis is UTI-focused only; no renal function endpoints.
Effect size: Non-significant
View on PubMed

🏛️Regulatory & authoritative positionsL4/L5 · FDA / EMA / NIH ODS / Cochrane / Mayo …

L4a US FDA
Cautious
Advanced U-Tract consists of D-mannose, which is used to help prevent bacteria from adhering to the walls of the urinary tract and reduce the occurrence of urinary tract infections. ... Therefore, this product is intended for treatment of diseases that are not amenable to self-diagnosis or treatment without the supervision of a licensed practitioner. As such, adequate directions cannot be writt… source↗
L4b EU EFSA
Against
L4c UK NHS
Cautious
D-mannose – a sugar you can buy as a powder or tablets to take every day source↗
L4d TW TFDA / 衛福部
Neutral
D-甘露糖屬自然界存在的單糖,為葡萄糖異構體,可以從植物與微生物中獲得,被廣泛應用於食品、化妝品以及醫藥業等領域。 source↗
L5c Cleveland Clinic
Not addressed
L5e Specialty Society (condition-mapped)
Not addressed
PMID 100% verifiedevery citation checked via NCBI Entrez
🔬3 PubMed studiesindependently re-checked by multiple sub-agents
engine_version: v1.0 claim_id: CLM-COND-kidney-disease-INT-d-mannose-001 繁體中文版 →