A Prediction Model for Detecting Dysthyroid Optic Neuropathy Based on Clinical Factors and Imaging Markers of the Optic Nerve and Cerebrospinal Fluid in the Optic Nerve Sheath

Hong-yu Wu, Ban Luo, Gang Yuan, Qiu-xia Wang, Ping Liu, Ya-li Zhao, Lin-han Zhai, Wen-zhi Lv, Jing Zhang, Lang Chen

Current Medical Science ›› 2024, Vol. 44 ›› Issue (4) : 827-832.

Current Medical Science ›› 2024, Vol. 44 ›› Issue (4) : 827-832. DOI: 10.1007/s11596-024-2890-2
Original Article

A Prediction Model for Detecting Dysthyroid Optic Neuropathy Based on Clinical Factors and Imaging Markers of the Optic Nerve and Cerebrospinal Fluid in the Optic Nerve Sheath

Author information +
History +

Abstract

Objective

This study aimed to develop and test a model for predicting dysthyroid optic neuropathy (DON) based on clinical factors and imaging markers of the optic nerve and cerebrospinal fluid (CSF) in the optic nerve sheath.

Methods

This retrospective study included patients with thyroid-associated ophthalmopathy (TAO) without DON and patients with TAO accompanied by DON at our hospital. The imaging markers of the optic nerve and CSF in the optic nerve sheath were measured on the water-fat images of each patient and, together with clinical factors, were screened by Least absolute shrinkage and selection operator. Subsequently, we constructed a prediction model using multivariate logistic regression. The accuracy of the model was verified using receiver operating characteristic curve analysis.

Results

In total, 80 orbits from 44 DON patients and 90 orbits from 45 TAO patients were included in our study. Two variables (optic nerve subarachnoid space and the volume of the CSF in the optic nerve sheath) were found to be independent predictive factors and were included in the prediction model. In the development cohort, the mean area under the curve (AUC) was 0.994, with a sensitivity of 0.944, specificity of 0.967, and accuracy of 0.901. Moreover, in the validation cohort, the AUC was 0.960, the sensitivity was 0.889, the specificity was 0.893, and the accuracy was 0.890.

Conclusions

A combined model was developed using imaging data of the optic nerve and CSF in the optic nerve sheath, serving as a noninvasive potential tool to predict DON.

Cite this article

Download citation ▾
Hong-yu Wu, Ban Luo, Gang Yuan, Qiu-xia Wang, Ping Liu, Ya-li Zhao, Lin-han Zhai, Wen-zhi Lv, Jing Zhang, Lang Chen. A Prediction Model for Detecting Dysthyroid Optic Neuropathy Based on Clinical Factors and Imaging Markers of the Optic Nerve and Cerebrospinal Fluid in the Optic Nerve Sheath. Current Medical Science, 2024, 44(4): 827‒832 https://doi.org/10.1007/s11596-024-2890-2

References

[1]
Khong JJ, Finch S, De Silva C, et al.. Risk Factors for Graves’ Orbitopathy; the Australian Thyroid-Associated Orbitopathy Research (ATOR) Study. J Clin Endocrinol Metab, 2016, 101(7): 2711-2720
CrossRef Google scholar
[2]
Bartalena L, Wiersinga WM, Pinchera A. Graves’ ophthalmopathy: state of the art and perspectives. J Endocrinol Invest, 2004, 27(3): 295-301
CrossRef Google scholar
[3]
Neigel JM, Rootman J, Belkin RI, et al.. Dysthyroid Optic Neuropathy. Ophthalmology, 1988, 95(11): 1515-1521
CrossRef Google scholar
[4]
McKeag D, Lane C, Lazarus JH, et al.. Clinical features of dysthyroid optic neuropathy: a European Group on Graves’ Orbitopathy (EUGOGO) survey. Br J Ophthalmol, 2007, 91(4): 455-458
CrossRef Google scholar
[5]
Nugent RA, Belkin RI, Neigel JM, et al.. Graves orbitopathy: correlation of CT and clinical findings. Radiology, 1990, 177(3): 675-682
CrossRef Google scholar
[6]
Saeed P, Tavakoli Rad S, Bisschop PHLT. Dysthyroid Optic Neuropathy. Ophthalmic Plast Reconstr Surg, 2018, 34(4SSuppl1): S60-S67
CrossRef Google scholar
[7]
Riemann CD, Foster JA, Kosmorsky GS. Direct orbital manometry in patients with thyroid-associated orbitopathy. Ophthalmology, 1999, 106(7): 1296-1302
CrossRef Google scholar
[8]
Perez-Lopez M, Sales-Sanz M, Rebolleda G, et al.. Retrobulbar ocular blood flow changes after orbital decompression in Graves’ ophthalmopathy measured by color Doppler imaging. Invest Ophthalmol Vis Sci, 2011, 52(8): 5612-5617
CrossRef Google scholar
[9]
Soni CR, Johnson LN. Visual Neuropraxia and Progressive Vision Loss from Thyroid-Associated Stretch Optic Neuropathy. Eur J Ophthal, 2010, 20(2): 429-436
CrossRef Google scholar
[10]
Dodds NI, Atcha AW, Birchall D, et al.. Use of high-resolution MRI of the optic nerve in Graves’ ophthalmopathy. Br J Radiol, 2009, 82(979): 541-544
CrossRef Google scholar
[11]
Rutkowska-Hinc B, Maj E, Jablonska A, et al.. Prevalence of Radiological Signs of Dysthyroid Optic Neuropathy in Magnetic Resonance Imaging in Patients with Active, Moderate-to-Severe, and Very Severe Graves Orbitopathy. Eur Thyroid J, 2018, 7(2): 88-94
CrossRef Google scholar
[12]
Kaichi Y, Tanitame K, Itakura H, et al.. Orbital Fat Volumetry and Water Fraction Measurements Using T2-Weighted FSE-IDEAL Imaging in Patients with Thyroid-Associated Orbitopathy. AJNR Am J Neuroradiol, 2016, 37(11): 2123-2128
CrossRef Google scholar
[13]
Das T, Roos JCP, Patterson AJ, et al.. T2-relaxation mapping and fat fraction assessment to objectively quantify clinical activity in thyroid eye disease: an initial feasibility study. Eye (Lond), 2019, 33(2): 235-243
CrossRef Google scholar
[14]
Reeder SB, Pineda AR, Wen Z, et al.. Iterative decomposition of water and fat with echo asymmetry and least-squares estimation (IDEAL): application with fast spin-echo imaging. Magn Reson Med, 2005, 54(3): 636-644
CrossRef Google scholar
[15]
Yu H, Reeder SB, Shimakawa A, et al.. Field map estimation with a region growing scheme for iterative 3-point water-fat decomposition. Magn Reson Med, 2005, 54(4): 1032-1039
CrossRef Google scholar
[16]
Bartley GB, Gorman CA. Diagnostic Criteria for Graves’ Ophthalmopathy. Am J Ophthalmol, 1995, 119(6): 792-795
CrossRef Google scholar
[17]
Wu H, Luo B, Yuan G, et al.. The diagnostic value of the IDEAL-T2WI sequence in dysthyroid optic neuropathy: a quantitative analysis of the optic nerve and cerebrospinal fluid in the optic nerve sheath. Eur Radiol, 2021, 31(10): 7419-7428
CrossRef Google scholar
[18]
Humbert IA, Reeder SB, Porcaro EJ, et al.. Simultaneous estimation of tongue volume and fat fraction using IDEAL-FSE. J Magn Reson Imaging, 2008, 28(2): 504-508
CrossRef Google scholar
[19]
Ollitrault A, Charbonneau F, Herdan ML, et al.. Dixon-T2WI magnetic resonance imaging at 3 tesla outperforms conventional imaging for thyroid eye disease. Eur Radiol, 2021, 31(7): 5198-5205
CrossRef Google scholar
[20]
Costa DN, Pedrosa I, McKenzie C, et al.. Body MRI using IDEAL. AJR Am J Roentgenol, 2008, 190(4): 1076-1084
CrossRef Google scholar
[21]
Nardo L, Karampinos DC, Lansdown DA, et al.. Quantitative assessment of fat infiltration in the rotator cuff muscles using water-fat MRI. J Magn Reson Imaging, 2014, 39(5): 1178-1185
CrossRef Google scholar
[22]
Nedergaard M, Goldman SA. Glymphatic failure as a final common pathway to dementia. Science, 2020, 370(6512): 50-56
CrossRef Google scholar
[23]
Mathieu E, Gupta N, Ahari A, et al.. Evidence for Cerebrospinal Fluid Entry Into the Optic Nerve via a Glymphatic Pathway. Invest Ophthalmol Vis Sci, 2017, 58(11): 4784-4791
CrossRef Google scholar
[24]
Mathieu E, Gupta N, Paczka-Giorgi LA, et al.. Reduced Cerebrospinal Fluid Inflow to the Optic Nerve in Glaucoma. Invest Ophthalmol Vis Sci, 2018, 59(15): 5876-5884
CrossRef Google scholar
[25]
Suzuki H, Oku H, Horie T, et al.. Changes in expression of aquaporin-4 and aquaporin-9 in optic nerve after crushing in rats. PLoS One, 2014, 9(12): e114694
CrossRef Google scholar
[26]
Lambin P, Rios-Velazquez E, Leijenaar R, et al.. Radiomics: extracting more information from medical images using advanced feature analysis. Eur J Cancer, 2012, 48(4): 441-446
CrossRef Google scholar

Accesses

Citations

Detail

Sections
Recommended

/