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Portrait of the Inflammatory Response to Radioiodine Therapy in Female Patients with Differentiated Thyroid Cancer with/without Type 2 Diabetes Mellitus.

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Cancers 📖 저널 OA 100% 2021: 20/20 OA 2022: 79/79 OA 2023: 89/89 OA 2024: 156/156 OA 2025: 683/683 OA 2026: 512/512 OA 2021~2026 2023 Vol.15(15)
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: differentiated thyroid cancer (DTC) associated with type 2 diabetes mellitus (T2DM) and obesity
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Considering the immune response to I therapy, the two groups of patients can be seen as a synchronous portrait of two sides. The explanation could lie in the different radiosensitivity of T and B lymphocytes, with T lymphocytes being predominant in patients with DTC/-T2DM and, most likely, B lymphocytes being predominant in T2DM.

Stanciu AE, Hurduc A, Stanciu MM, Gherghe M, Gheorghe DC, Prunoiu VM

📝 환자 설명용 한 줄

No clinical studies have investigated the effect of radioiodine (I)-targeted therapy on the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) as inflammatory response markers

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↓ .bib ↓ .ris
APA Stanciu AE, Hurduc A, et al. (2023). Portrait of the Inflammatory Response to Radioiodine Therapy in Female Patients with Differentiated Thyroid Cancer with/without Type 2 Diabetes Mellitus.. Cancers, 15(15). https://doi.org/10.3390/cancers15153793
MLA Stanciu AE, et al.. "Portrait of the Inflammatory Response to Radioiodine Therapy in Female Patients with Differentiated Thyroid Cancer with/without Type 2 Diabetes Mellitus.." Cancers, vol. 15, no. 15, 2023.
PMID 37568611 ↗

Abstract

No clinical studies have investigated the effect of radioiodine (I)-targeted therapy on the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) as inflammatory response markers in patients with differentiated thyroid cancer (DTC) associated with type 2 diabetes mellitus (T2DM) and obesity. This study aimed to assess the relationship between blood radioactivity, body mass index (BMI), and peripheral blood cells three days after I intake in 56 female patients without T2DM (DTC/-T2DM) vs. 24 female patients with T2DM (DTC/+T2DM). Blood radioactivity, measured three days after I intake, was significantly lower in the DTC/+T2DM than in the DTC/-T2DM patients (0.7 mCi vs. 1.5 mCi, < 0.001). The relationship between blood radioactivity and BMI (r = 0.83, < 0.001), blood radioactivity and NLR (r = 0.53, = 0.008), and BMI and NLR (r = 0.58, = 0.003) indicates a possible connection between the bloodstream I uptake and T2DM-specific chronic inflammation. In patients without T2DM, I therapy has immunosuppressive effects, leading to increased NLR (19.6%, = 0.009) and PLR (39.1%, = 0.002). On the contrary, in the chronic inflammation context of T2DM, I therapy amplifies immune metabolism, leading to a drop in NLR (10%, = 0.032) and PLR (13.4%, = 0.021). Our results show that, in DTC/+T2DM, the bidirectional crosstalk between neutrophils and obesity may limit I uptake in the bloodstream. Considering the immune response to I therapy, the two groups of patients can be seen as a synchronous portrait of two sides. The explanation could lie in the different radiosensitivity of T and B lymphocytes, with T lymphocytes being predominant in patients with DTC/-T2DM and, most likely, B lymphocytes being predominant in T2DM.

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