Manganese Exposure in Occupational Settings: Disruptions in Endothelial Function and Thyroid Regulation

<b>Background:</b> Manganese (Mn) exposure is common in welding and metal-processing occupations and has been implicated in both thyroid disruption and endothelial dysfunction through oxidative and nitric-oxide-related pathways. However, endocrine and vascular biomarkers have rarely been examined together in occupational settings. <b>Methods:</b> In this cross-sectional study, 95 Mn-exposed workers and 95 non-exposed controls were evaluated. Whole-blood Mn, triiodothyronine (T3), thyroxine (T4), thyroid-stimulating hormone (TSH), asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), arginine and citrulline were measured using validated Inductively Coupled Plasma-Mass Spectrometer and chemiluminescent immunoassays. Group differences were assessed using independent samples t-tests, and exposure-biomarker associations were evaluated using Pearson correlations (<i>p</i> < 0.05). <b>Results:</b> Mn-exposed workers had significantly higher blood Mn levels than controls (19.82 ± 4.54 vs. 10.22 ± 3.07 µg/L; <i>p</i> < 0.001). Thyroid hormones (T3, T4, and TSH) were significantly lower among Mn workers, representing a non-classical hormonal pattern, including T3 (2.47 ± 0.31 vs. 3.14 ± 0.42 ng/L; <i>p</i> < 0.001), T4 (1.02 ± 0.13 vs. 1.21 ± 0.18 ng/L; <i>p</i> < 0.001), and TSH (1.75 ± 0.53 vs. 2.88 ± 0.37 mIU/L; <i>p</i> < 0.001). Endothelial biomarkers also differed: ADMA (0.26 ± 0.14 vs. 0.19 ± 0.08 µmol/L; <i>p</i> < 0.001) and SDMA (0.24 ± 0.06 vs. 0.20 ± 0.03 µmol/L; <i>p</i> < 0.001) were higher, while citrulline was lower (18.77 ± 10.23 vs. 22.82 ± 6.70 µmol/L; <i>p</i> = 0.002). In Mn workers, blood Mn showed negative correlations with T3 (r = -0.535, <i>p</i> < 0.01), T4 (r = -0.331, <i>p</i> < 0.01), and TSH (r = -0.652, <i>p</i> < 0.01), and positive correlations with ADMA (r = 0.205, <i>p</i> < 0.05) and SDMA (r = 0.193, <i>p</i> < 0.05). <b>Conclusions:</b> These findings indicate measurable differences in thyroid hormones and dimethylarginine-related endothelial markers among Mn-exposed workers. While the cross-sectional design precludes causal inference, the combined pattern suggests a possible unusual biological response involving both endocrine regulation and nitric-oxide-related pathways. Further longitudinal studies incorporating oxidative stress markers, co-exposure assessment, and functional endothelial testing are needed to clarify the biological relevance of these associations.

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Journal
Metabolites
Published
2025-12-19
DOI
https://doi.org/10.3390/metabo16010001
Primary Topic
Heavy Metal Exposure and Toxicity
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article
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article

Manganese Exposure in Occupational Settings: Disruptions in Endothelial Function and Thyroid Regulation

Deniz Özkan Vardar, Melih Gaffar Gözükara, Servet Birgin İritaş, Serdar Deniz et al.
Metabolites
Heavy Metal Exposure and Toxicity
article

Manganese Exposure in Occupational Settings: Disruptions in Endothelial Function and Thyroid Regulation

Deniz Özkan Vardar, Melih Gaffar Gözükara, Servet Birgin İritaş, Serdar Deniz, Vugar Ali Türksoy, Özlem İRİTAŞ, Lütfiye Tutkun, Murat Büyükşekerci, Engіn Tutkun
article en

Abstract

<b>Background:</b> Manganese (Mn) exposure is common in welding and metal-processing occupations and has been implicated in both thyroid disruption and endothelial dysfunction through oxidative and nitric-oxide-related pathways. However, endocrine and vascular biomarkers have rarely been examined together in occupational settings. <b>Methods:</b> In this cross-sectional study, 95 Mn-exposed workers and 95 non-exposed controls were evaluated. Whole-blood Mn, triiodothyronine (T3), thyroxine (T4), thyroid-stimulating hormone (TSH), asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), arginine and citrulline were measured using validated Inductively Coupled Plasma-Mass Spectrometer and chemiluminescent immunoassays. Group differences were assessed using independent samples t-tests, and exposure-biomarker associations were evaluated using Pearson correlations (<i>p</i> < 0.05). <b>Results:</b> Mn-exposed workers had significantly higher blood Mn levels than controls (19.82 ± 4.54 vs. 10.22 ± 3.07 µg/L; <i>p</i> < 0.001). Thyroid hormones (T3, T4, and TSH) were significantly lower among Mn workers, representing a non-classical hormonal pattern, including T3 (2.47 ± 0.31 vs. 3.14 ± 0.42 ng/L; <i>p</i> < 0.001), T4 (1.02 ± 0.13 vs. 1.21 ± 0.18 ng/L; <i>p</i> < 0.001), and TSH (1.75 ± 0.53 vs. 2.88 ± 0.37 mIU/L; <i>p</i> < 0.001). Endothelial biomarkers also differed: ADMA (0.26 ± 0.14 vs. 0.19 ± 0.08 µmol/L; <i>p</i> < 0.001) and SDMA (0.24 ± 0.06 vs. 0.20 ± 0.03 µmol/L; <i>p</i> < 0.001) were higher, while citrulline was lower (18.77 ± 10.23 vs. 22.82 ± 6.70 µmol/L; <i>p</i> = 0.002). In Mn workers, blood Mn showed negative correlations with T3 (r = -0.535, <i>p</i> < 0.01), T4 (r = -0.331, <i>p</i> < 0.01), and TSH (r = -0.652, <i>p</i> < 0.01), and positive correlations with ADMA (r = 0.205, <i>p</i> < 0.05) and SDMA (r = 0.193, <i>p</i> < 0.05). <b>Conclusions:</b> These findings indicate measurable differences in thyroid hormones and dimethylarginine-related endothelial markers among Mn-exposed workers. While the cross-sectional design precludes causal inference, the combined pattern suggests a possible unusual biological response involving both endocrine regulation and nitric-oxide-related pathways. Further longitudinal studies incorporating oxidative stress markers, co-exposure assessment, and functional endothelial testing are needed to clarify the biological relevance of these associations.

MetabolitesVol. 16(1)
Ministry of Agriculture and Forestry (LA), Yozgat Bozok Üniversitesi (TR), Ankara Atatürk Eğitim ve Araştırma Hastanesi (TR), Psychiatric Association of Turkey (TR), Malatya Turgut Özal Üniversitesi (TR), Lokman Hekim Üniversitesi (TR), Turkish Electro Technology (Turkey) (TR), Ankara Yıldırım Beyazıt University (TR), General Directorate of Forestry (TR), Turgut Özal University (TR)
Openalex Percentile: Top 50%
Heavy Metal Exposure and Toxicity
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