Evidence map›Paper›PMID 40361175›Full record

ArticleBMC pharmacology & toxicology2025

Predictive role of cystatin C and increased proteinuria in early assessment of acute renal toxicity in patient poisoned by nephrotoxic drugs and poisons.

Esam Mohammed Abdallah Ali, Emad Ahmad Mohamad Yousef, Maha Abd El-Hamed Helal, Mohammed Hamdi Mohammed, Meray Medhat Shokry Zaghary, Marwa Ahmed Hasb Elnabi

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Toxidromes.Nature reviews. Disease primers · 2026
    Review
  2. Article
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.

Esam Mohammed Abdallah AliForensic Medicine & Clinical Toxicology Department, Faculty of Medicine, Sohag University, Sohag, 82524, Egypt.
Emad Ahmad Mohamad YousefInternal Medicine Department, Faculty of Medicine, Sohag University Sohag, Sohag, 82524, Egypt.
Maha Abd El-Hamed HelalForensic Medicine & Clinical Toxicology Department, Faculty of Medicine, Sohag University, Sohag, 82524, Egypt.
Mohammed Hamdi MohammedForensic Medicine & Clinical Toxicology Department, Faculty of Medicine, Sohag University, Sohag, 82524, Egypt.
Meray Medhat Shokry ZagharyForensic Medicine & Clinical Toxicology Department, Faculty of Medicine, Sohag University, Sohag, 82524, Egypt. meraymedhat@med.sohag.edu.eg.ORCID 0000-0002-3787-2158
Marwa Ahmed Hasb ElnabiForensic Medicine & Clinical Toxicology Department, Faculty of Medicine, Sohag University, Sohag, 82524, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is prevalent in critical care, often due to nephrotoxic drug exposure, which accounts for significant morbidity and mortality. Current biomarkers, like serum creatinine, lack sensitivity for early detection of nephrotoxicity.

aimThis study evaluates proteinuria and serum cystatin C as early indicators of nephrotoxicity in acutely poisoned patients at Sohag University Hospitals.

methodsThis prospective study involved 100 acutely poisoned patients with nephrotoxic effects admitted to Sohag University Hospitals from April to August 2021. Inclusion criteria required symptomatic patients who provided at least four blood or urine samples, including one within 24 h post-ingestion. AKI was classified using the Acute Kidney Injury Network (AKIN) criteria, with baseline serum creatinine estimated from the lowest value during hospitalization. Biomarkers, including serum creatinine and cystatin C, were measured using standard assays for analysis.

resultsThe study included 100 patients aged 2 to 58 years, predominantly male (72%). Most participants were from rural areas (82%). Serum creatinine levels significantly increased from day 1 (mean ± SD: 1.67 ± 0.6 mg/dL) to day 2 (mean ± SD: 2.98 ± 1.35 mg/dL). Significant predictors of acute renal toxicity included serum creatinine on both days (P < 0.001), proteinuria ACR (P = 0.023), and cystatin C (P < 0.001). Cystatin C had the highest predictive value (AUC = 0.993), while proteinuria ACR and day 2 serum creatinine showed significant predictive capabilities (AUCs of 0.805 and 0.873, respectively).

conclusionIn conclusion, proteinuria and cystatin C are reliable predictors for early nephrotoxicity detection in acutely poisoned patients at Sohag University Hospitals. These biomarkers effectively indicate and assess the severity of kidney injury caused by toxicity.

Indexed as

Acute Kidney InjuryCystatin CPoisoningProteinuriaAdolescentAdultBiomarkersChildChild, PreschoolCreatinineFemaleHumansMaleMiddle AgedProspective StudiesYoung AdultBiomarkersCreatinineCystatin CAcute kidney injuryAcute poisoningCystatin CNephrotoxicityProteinuria

Identifiers

PMID40361175
PMCPMC12076890

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.