Abstract

ObjectivePrediction of therapy response to intravenous methylprednisolone pulses (ivMP) is crucial for thyroid-associated ophthalmopathy (TAO). Image histograms may offer sensitive imaging biomarkers for therapy effect prediction. This study aimed to investigate whether pretherapeutic, multiparametric T2 relaxation time(T2RT) histogram features of extraocular muscles (EOMs) can be used to predict therapy response.Materials and MethodsForty-five active and moderate-severe TAO patients, who were treated with standard ivMP and underwent orbital MRI before therapy, were retrospectively included in this study. The patients were divided into responsive (n = 24, 48 eyes) and unresponsive group(n = 21, 42 eyes) according to clinical evaluation. Baseline clinical features of patients and histogram-derived T2RT parameters of the EOMs were analyzed and compared. Logistic regression model was conducted to determine independent predictors, and a histogram features nomogram was formulated for personalized prediction.ResultsResponsive group displayed lower values for 5th, 10th percentiles (P < 0.050, respectively), and higher values for 75th, 90th, and 95th percentiles, skewness, entropy, and inhomogeneity (P < 0.050, respectively) than unresponsive group. Multivariate logistic regression analysis showed that 95th percentile of >88.1 [odds ratio (OR) = 12.078; 95% confidence interval (CI) = 3.98–36.655, p < 0.001], skewness of >0.31 (OR = 3.935; 95% CI = 2.28–6.788, p < 0.001) and entropy of >3.41 (OR = 4.375; 95% CI = 2.604–7.351, p < 0.001) were independent predictors for favorable response. The nomogram integration of three independent predictors demonstrated optimal predictive efficiency, with a C-index of 0.792.ConclusionsPre-treatment volumetric T2RT histogram features of EOMs could function to predict the response to ivMP in patients with TAO. The nomogram based on histogram features facilitates the selection of patients who will derive maximal benefit from ivMP.

Highlights

  • Thyroid-associated ophthalmopathy (TAO) is an autoimmune disorder affecting the orbital and periorbital tissues

  • The overall response to Intravenous methylprednisolone pulse (ivMP) therapy is not very satisfactory [1, 2], many patients exhibit non-response or progression [3]. This may relate to other complex pathogenesis of TAO, including helper T-cells, T-regulatory cells, and interleukin-17/23

  • Therapeutic response prediction is essential for patienttailored treatment, as it helps to identify those patients who will truly benefit from the potentially toxic ivMP therapy, thereby both preventing overtreatment/futile treatment and optimizing the management of TAO

Read more

Summary

Introduction

Thyroid-associated ophthalmopathy (TAO) is an autoimmune disorder affecting the orbital and periorbital tissues. Intravenous methylprednisolone pulse (ivMP) remains the first-line treatment for active, moderate-to-severe TAO [1]. The overall response to ivMP therapy is not very satisfactory [1, 2], many patients exhibit non-response or progression [3]. This may relate to other complex pathogenesis of TAO, including helper T-cells, T-regulatory cells, and interleukin-17/23. Therapeutic response prediction is essential for patienttailored treatment, as it helps to identify those patients who will truly benefit from the potentially toxic ivMP therapy, thereby both preventing overtreatment/futile treatment and optimizing the management of TAO

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.