# Distribution of Toxic and Essential Elements in Autopsy Organs of Subjects Living in South-Eastern Poland

**Authors:** Wojciech Flieger, Przemysław Niedzielski, Michał Flieger, Zofia Wojciechowska, Aleksandra Proch, Jędrzej Proch, Alicja Forma, Andrzej Torbicz, Dariusz Majerek, Grzegorz Teresiński, Jacek Baj, Eliasz Dzierżyński, Jolanta Flieger

PMC · DOI: 10.3390/ijms27062585 · International Journal of Molecular Sciences · 2026-03-11

## TL;DR

This study analyzed heavy metal concentrations in organs of people from South-Eastern Poland to understand how environmental exposure affects health.

## Contribution

The study reveals organ-specific accumulation patterns of toxic and essential elements in a moderately industrialized region.

## Key findings

- The liver preferentially sequesters essential elements like Zn, Se, Mn, and Cu.
- Toxic metals like Cd and Pb accumulate in the liver and Cr in the lungs due to long biological half-lives.
- Strong correlations between Se–Zn and Se–Cu suggest integrated antioxidant responses.

## Abstract

Chronic exposure to heavy metals poses significant health risks. This study analyzed the concentrations of toxic (Cr, Pb, Cd, Ni) and essential (Cu, Zn, Se, Mn) elements in autopsy samples (the frontal pole area of the brain, the 6th intercostal space of the liver, and lungs (average of left and right lung samples) from 45 residents of South-Eastern Poland using ICP-MS. The aim was to determine the average body burden and organ-specific accumulation in a moderately industrialized region. HDBSCAN clustering revealed highly homogeneous elemental profiles, suggesting a unifying influence of local environmental factors. The liver acted as a metabolic hub, showing preferential sequestration (p < 0.0001) of essential elements (Zn, Se, Mn, Cu) regulated by homeostatic mechanisms. Toxic metals exhibited ‘metabolic trap’ patterns, particularly Cd and Pb in the liver and Cr in the lungs, due to their long biological half-lives. Strong positive correlations (Se–Zn, Se–Cu) indicated integrated antioxidant responses, while toxic pairs (Cr–Ni, Pb–Cd) suggested shared exposure pathways and molecular mimicry via transporters such as DMT1. Results confirmed long-term bioaccumulation, with toxic elements in the brain remaining below 0.25 µg/g. In the lungs, the accumulation hierarchy (Pb > Mn > Cd > Cr) reflected inhalation exposure. These findings emphasize the role of organ-specific sequestration in assessing long-term environmental exposure.

## Linked entities

- **Chemicals:** Cr (PubChem CID 23976), Pb (PubChem CID 5352425), Cd (PubChem CID 23973), Ni (PubChem CID 934), Cu (PubChem CID 23978), Zn (PubChem CID 23994), Se (PubChem CID 5460640), Mn (PubChem CID 23930)

## Full-text entities

- **Genes:** DMRT1 (doublesex and mab-3 related transcription factor 1) [NCBI Gene 1761] {aka CT154, DMT1}
- **Diseases:** Toxic (MESH:D064420)
- **Chemicals:** Se (MESH:D012643), Cu (MESH:D003300), Pb (MESH:D007854), Zn (MESH:D015032), heavy metals (MESH:D019216), Cr (MESH:D002857), Mn (MESH:D008345), Cd (MESH:D002104), Ni (MESH:D009532)

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026681/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026681/full.md

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Source: https://tomesphere.com/paper/PMC13026681