Evidence map›Paper›PMID 41606724›Full record

ArticleBMC nephrology2026

Mechanism for adverse renal effects from heavy metals exposure in the CRIC study.

Robert M Taylor, Justin T Baca, Vernon S Pankratz, Wei Yang, Xue Wang, Tanika Kelly, James P Lash, Hernan Rincon-Choles, Bernard G Jaar, Madhumita Jena Mohanty and 6 more

Abstract readMulticenter Study
In one paragraph

Article in BMC nephrology, 2026. 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

16 authors.

Robert M TaylorDepartment of Pharmaceutical Sciences, The University of New Mexico, Albuquerque, NM, 87131, USA.
Justin T BacaDepartment of Emergency Medicine, The University of New Mexico, Albuquerque, NM, 87131, USA.
Vernon S PankratzDepartment of Internal Medicine, The University of New Mexico, Albuquerque, NM, 87131, USA.
Wei YangDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Xue WangDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Tanika KellyDepartment of Medicine, University of Illinois Chicago, Chicago, IL, 60612, USA.
James P LashDepartment of Medicine, University of Illinois Chicago, Chicago, IL, 60612, USA.
Hernan Rincon-CholesDepartment of Kidney Medicine, Cleveland Clinic Foundation, Cleveland, OH, 44195, USA.
Bernard G JaarDivision of Nephrology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, 21205, USA.
Madhumita Jena MohantyDepartment of Internal Medicine, Wayne State University, Detroit, MI, 48201, USA.
Vecihi BatumanDepartment of Medicine, Tulane School of Medicine, New Orleans, LA, 70112, USA.
Jing ChenDepartment of Medicine, Tulane School of Medicine, New Orleans, LA, 70112, USA.
Giselle R SosaDivision of Nephrology, Department of Internal Medicine, Albuquerque, NM, 87131, USA.
Mark UnruhDivision of Nephrology, Department of Internal Medicine, Albuquerque, NM, 87131, USA.
Vallabh ShahDepartment of Internal Medicine and Biochemistry and Molecular Biology, The University of New Mexico, Albuquerque, NM, 87131, USA. vshah@salud.unm.edu.
CRIC Study Investigators

Funding

Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
Tulane COBRE in Cardiometabolic Diseases Clinical Research CoreP20GM109036 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI JING CHEN · 2016 to 2026
$25.3M
American Indian CRIC Study of Diabetic Kidney Disease and Alzheimer Disease.R01DK119199 · NIDDK · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI SHAH, VALLABH O, UNRUH, MARK LYNN · 2019 to 2023
$3.7M
Clinical and Translational Science Center, University of New Mexico UL1TR001449CTSA UL1RR029879Kaiser Permanente NIH/NCRR UCSF-CTSI UL1 RR-024131NCATS NIH HHS UL1TR000003NIDDK NIH HHS U01DK060990, U01DK060984, U01DK061022, U01DK061021, U01DK061028, U01DK060980, U01DK060963, U01DK060902 and U24DK060990NIGMS NIH HHS P20 GM109036NIH HHS R01DK119199
6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) poses a major public health challenge, resulting in substantial illness, death, and financial strain. The potential role of environmental factors, such as heavy metal (HM) exposure, in the exacerbation of the disease is increasingly recognized but not well understood. This study aims to shed light on the impact of HMs on the progression of CKD.

methodsIn this study, we examined nail clippings and plasma samples from 20 participants enrolled in the Chronic Renal Insufficiency Cohort (CRIC), a multi-center study designed to investigate risk factors for CKD progression and cardiovascular outcomes. HM concentrations were quantified using inductively coupled plasma mass spectrometry (ICP/MS). We selected participants from two groups based on CKD progression: stable disease (n = 10) and fast-progressing disease (n = 10). We descriptively summarized variables within the groups and used Mann-Whitney and Fisher’s exact tests for between-group comparisons of continuous and categorical variables, respectively.

resultsBaseline demographic characteristics differed between stable and fast-progressors, with fast-progressors having higher body mass index (BMI) and higher systolic blood pressure. Distinct patterns in HM concentrations were observed. Subjects with more rapid CKD progression displayed higher median baseline metal burdens (293 µg/g) compared to those with stable disease (267 µg/g), but the differences did not reach statistical significance. Markers of ER stress, mitochondrial stress, and inflammation did not show statistically significant differences.

conclusionThis study offers preliminary data regarding a potential association between HM exposure and progression of CKD. Although comparisons did not reach statistical significance, they suggest potential pathways through which HMs may influence disease progression. Future studies with larger cohorts are necessary to validate these findings, improve statistical power, and further elucidate the roles of HMs in CKD progression. This research underscores the importance of considering environmental factors in the management of chronic diseases.

Indexed as

Environmental ExposureMetals, HeavyRenal Insufficiency, ChronicAdultCohort StudiesDisease ProgressionFemaleHumansMaleMiddle AgedNailsMetals, HeavyCellular stressChronic kidney disease (CKD)Endoplasmic reticulum (ER) stressHeavy metal exposureInflammationMetalloidsMitochondrial stressNail clippings

Identifiers

PMID41606724
PMCPMC12924355

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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.