# Integrative Analysis of Biochemical, Hormonal, and Histopathological Profiles in Thyroid Nodules: A Seven-Year Retrospective Study

**Authors:** Sergiu-Ciprian Matei, Mervat Matei, Sorin Ursoniu, Anna Laura Maiozzi, Ana Silvia Corlan, Bianca Roxana Natarâş, Flavia Medana Petrașcu, Mihaela Maria Vlad, Diana Szekely, Flavia Zara, Cristina Stefania Dumitru

PMC · DOI: 10.3390/biomedicines14010010 · Biomedicines · 2025-12-20

## TL;DR

This study found that standard clinical and biochemical markers are not effective in distinguishing between benign and malignant thyroid nodules.

## Contribution

The study provides evidence that routine markers have limited value for preoperative risk assessment in thyroid nodules.

## Key findings

- Most clinical and biochemical parameters showed no significant differences among benign, benign–malignant, and multiple malignant thyroid nodule groups.
- Neutrophil and lymphocyte counts showed minor differences but lacked strong discriminatory power.
- Common markers like TSH, FT3, and thyroid dimensions failed to distinguish between histopathological patterns.

## Abstract

Background/Objectives: Thyroid nodules exhibit substantial histopathological variability, and systemic markers that differentiate benign from malignant patterns remain poorly defined. This study evaluated clinical, biochemical, hormonal, and histopathological characteristics in patients undergoing total thyroidectomy for nodular thyroid disease. Methods: A retrospective cohort of 926 patients operated between 2017 and 2024 was analyzed. Patients were classified as: Group 1—benign lesions; Group 2—benign–malignant associations; Group 3—multiple malignant lesions. Demographic, biochemical, hormonal, and histopathological data were assessed using the Kruskal–Wallis and Mantel–Haenszel chi-square tests. Thyroid-specific tumor and autoimmunity markers (calcitonin, thyroglobulin, anti-thyroglobulin antibodies, and thyroid peroxidase antibodies) were not included in the comparative analyses due to their non-uniform availability across the retrospective cohort. Results: Most clinical and biochemical parameters showed no significant differences among the three groups, including TSH (p = 0.122), FT3 (p = 0.560), glycemia (p = 0.829), creatinine (p = 0.193), fibrinogen (p = 0.535), and thyroid dimensions (length p = 0.401, width p = 0.183, thickness p = 0.667, and total thyroid mass p = 0.109). Neutrophil count differed in the overall comparison (p = 0.021), although absolute differences were small, and lymphocyte counts were modestly lower in patients with multiple malignant lesions compared with benign disease (p = 0.009). Comorbidities and BMI were similarly distributed across groups (all p > 0.05). Overall, routinely available clinical, biochemical, and hormonal parameters demonstrated limited discriminatory value between patients with different histopathological patterns. Conclusions: Standard clinical, biochemical, and hormonal markers showed minimal ability to reflect underlying histopathological patterns in patients with thyroid nodules, underscoring their limited utility for preoperative risk stratification.

## Full-text entities

- **Genes:** TPO (thyroid peroxidase) [NCBI Gene 7173] {aka MSA, TDH2A, TPX}, TG (thyroglobulin) [NCBI Gene 7038] {aka AITD3, TGN}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** benign disease (MESH:D004194), thyroid (MESH:D013966), Thyroid-specific tumor (MESH:D013964), nodular thyroid disease (MESH:D013959), Thyroid Nodules (MESH:D016606), malignant (MESH:D009369)
- **Chemicals:** creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12839253/full.md

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Source: https://tomesphere.com/paper/PMC12839253