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Purpose: Radiolabelled fibroblast activation protein inhibitors (FAPIs) are becoming increasingly important for imaging various tumour diseases. However, it is essential to be aware of potential pitfalls. Here, we investigate FAP expression in the thyroid gland in autoimmune thyroiditis (AIT).
Methods: AIT patients with pathological thyroid uptake on [Ga]Ga-FAPI PET were compared with glucose metabolism on 2-[F]FDG PET in terms of SUV/SUV/SUV/tissue-to-background ratio (TBR), and with a healthy control group.
Results: Between September 2019 and July 2021, 6 patients presented with a visually increased thyroid uptake and TBR on [Ga]Ga-FAPI PET. In the retrospective clinical work-up, all patients had known or newly diagnosed AIT. Compared to a matched healthy control group, FAP expression and glucose metabolism were significantly increased ([Ga]Ga-FAPI (SUV): 7.0 vs. 1.7; p = 0.004/(TBR): 6.8 vs. 1.7; p = 0.002; 2-[F]FDG (SUV): 3.9 vs. 1.4; p = 0.004/(TBR): 4.0 vs. 1.2; p = 0.041). However, there was no significant difference in median uptake between [Ga]Ga-FAPI and 2-[18F]FDG PET (SUV: 7.3 vs. 5.6; p = 0.104).
Conclusion: Patients with AIT show higher thyroid uptake on [Ga]Ga-FAPI and 2-[F]FDG PET. Incidental thyroid uptake is another pitfall in the interpretation of [Ga]Ga-FAPI PET and should prompt a clinical work-up.
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http://dx.doi.org/10.1186/s13550-024-01129-y | DOI Listing |
Clin Nucl Med
September 2025
Hepatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Hepatocellular carcinoma is one of the leading causes of cancer-related death worldwide. Immune checkpoint inhibitors (ICI) have improved progression and overall survival in patients progressing on sorafenib therapy. But activation of the immune system can lead to numerous immune-related adverse events.
View Article and Find Full Text PDFClin Chim Acta
September 2025
Pain Management Center, Hospital Angeles Mocel, Mexico City, Mexico.
Glucose metabolism alterations are frequently observed in patients with secretory pituitary adenomas. The most commonly secreted hormones in these tumors include prolactin, growth hormone (GH), adrenocorticotropic hormone (ACTH), and thyroid-stimulating hormone (TSH), all of which can disrupt glucose homeostasis through distinct pathophysiological mechanisms. Prolactin stimulates pancreatic β-cell proliferation, enhances insulin gene transcription, increases intracellular insulin content, and augments glucose-induced insulin secretion.
View Article and Find Full Text PDFJCI Insight
September 2025
Department of Internal Medicine, The University of Texas Medical Branch, Galveston, United States of America.
Maternal low thyroxine (T4) serum levels during the first trimester of pregnancy correlate with cerebral cortex volume and mental development of the progeny, but why neural cells during early fetal brain development are vulnerable to maternal T4 levels remains unknown. In this study, using iPSCs obtained from a boy with a loss-of-function mutation in MCT8-a transporter previously identified as critical for thyroid hormone uptake and action in neural cells-we demonstrate that thyroid hormones induce transcriptional changes that promote the progression of human neural precursor cells along the dorsal projection trajectory. Consistent with these findings, single-cell, spatial, and bulk transcriptomics from MCT8-deficient cerebral organoids and cultures of human neural precursor cells underscore the necessity for optimal thyroid hormone levels for these cells to differentiate into neurons.
View Article and Find Full Text PDFJ Radiol Prot
September 2025
National Cancer Institute Division of Cancer Epidemiology and Genetics, Bethesda, Maryland, UNITED STATES.
Exposure to radioactive iodine (radioiodine) during pregnancy and lactation poses unique risks to both mothers and their offspring due to altered iodine metabolism and heightened radiosensitivity. Existing biokinetic models, such as those developed by Berkovski, have provided a foundation for understanding iodine kinetics in these physiological states but lack integration with the latest International Commission on Radiological Protection (ICRP) reference model for non-pregnant adults. In this study, we developed integrated biokinetic models for pregnancy and lactation that are structurally consistent with the ICRP Publication 137 adult iodine model.
View Article and Find Full Text PDFAdv Mater
September 2025
Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Glucose consumption by tumors induces metabolic restriction of T cells, which results in immune evasion and tumor progression. Regulating cellular metabolism represents a promising strategy to enhance cancer immunotherapy; however, redirecting glucose utilization from tumor cells to T cells is challenging. Herein, the activation of cytotoxic T cells using engineered peptide coacervates (PCs) containing interferon alpha (IFNα) and membranized with metal-phenolic networks (MPNs) (PC-IFNα@MPNs), which promote glucose uptake and glycolysis, is reported.
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