Evidence map›Paper›PMID 42620295›Full record

ArticleToxicology reports2026

Integrated biomarker analysis of multi-organ effects following MDMA and alcohol co-consumption in Pakistan: A pilot study.

Anila Jaleel, Mahnoor Khan, Kiran Namoos, Muhammad Waleed Ibrahim, Junaid Majid Sheikh, Tahira Naseem, Shahila Jaleel, Ghulam Farid

Abstract read
In one paragraph

Article in Toxicology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Anila JaleelDepartment of Biochemistry, Shalamar Medical and Dental College, Lahore, Pakistan.
Mahnoor KhanBiochemistry and Chemical Pathology Dept, Shaikh Zayed Postgraduate Medical Institute, Lahore, Pakistan.
Kiran NamoosDepartment of Biochemistry, Shalamar Medical and Dental College, Lahore, Pakistan.
Muhammad Waleed IbrahimShalamar Medical and Dental College, Lahore, Pakistan.
Junaid Majid SheikhShalamar Medical and Dental College, Lahore, Pakistan.
Tahira NaseemBiochemistry and Chemical Pathology Dept, Shaikh Zayed Postgraduate Medical Institute, Lahore, Pakistan.
Shahila JaleelPathology Department, Shaikh Zayed Postgraduate Medical Institute, Lahore, Pakistan.
Ghulam FaridShalamar Medical & Dental College, Lahore, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy") is a widely abused recreational drug associated with multi-organ toxicity. Objective was to compare hepatic, renal, and systemic biochemical abnormalities after acute MDMA exposure alone and with alcohol. This cross-sectional pilot study was conducted at Sheikh Zayed bin Al Nahyan and Shalamar Medical and Dental Colleges, Pakistan. The study included 24 exposed participants (ecstasy-only n = 10; ecstasy and alcohol n = 14) and 20 controls. Blood samples were analyzed for AST (<37 U/L), ALT (<63 U/L), ALP (46-116 U/L), GGT (<55 U/L), LDH (81-234 U/L), Urea (10-50 mg/dl), Creatinine (0.7-1.4 mg/dL), Uric Acid (3.5-7.2 mg/dl), and CK (39-232 U/L). Marked hepatorenal biochemical injury was predefined as ALP > 3 times the laboratory specific upper limit of normal or serum urea > 150 mg/dl. Group comparison, age and sex adjusted multivariable linear regression and ROC analyses were performed. The study group exhibited significantly elevated hepatorenal biomarkers vs. controls. Median AST, ALT and ALP were117.0, 117.5 and 439.0 U/L, equivalent to 3.16, 1.86 and 3.78 x ULN, respectively. Median urea and creatinine levels were 172.5 mg/dL and 1.42 mg/dL respectively. No significant difference was found between ecstasy-only and ecstasy and alcohol after correction. Adjusted models showed significantly higher ALP, urea, and creatinine in both study groups versus controls. RSI and STI showed high apparent discrimination (AUC 1.000 and 0.890, respectively). Acute MDMA exposure was associated with marked hepatic and renal biochemical abnormalities. Alcohol co-consumption did not independently exacerbate organ damage. The RSI and STI are novel, cost-effective, and highly accurate tools for emergency triage using routine laboratory parameters.

Indexed as

3,4-MethylenedioxymethamphetamineAcute Kidney InjuryBiomarkersChemical and Drug Induced Liver InjuryEthanol

Identifiers

PMID42620295
PMCPMC13485660

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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.