Utility of Optical Coherence Tomography in the Diagnosis and Management of Optic Neuropathy in Patients with Fibrous Dysplasia

被引:4
作者
Pan, Kristen S. [1 ]
FitzGibbon, Edmond J. [2 ]
Vitale, Susan [3 ]
Lee, Janice S. [4 ]
Collins, Michael T. [1 ]
Boyce, Alison M. [1 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Skeletal Disorders & Mineral Homeostasis Sect, NIH, Bethesda, MD USA
[2] NEI, Sensorimotor Res Lab, NIH, Bldg 10, Bethesda, MD 20892 USA
[3] NEI, Div Epidemiol & Clin Applicat, NIH, Bethesda, MD 20892 USA
[4] Natl Inst Dent & Craniofacial Res, Craniofacial Anomalies & Regenerat Sect, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
OPTIC NEUROPATHY; FIBROUS DYSPLASIA; OPTICAL COHERENCE TOMOGRAPHY; RETINAL NERVE FIBER LAYER; NERVE-FIBER LAYER; MCCUNE-ALBRIGHT SYNDROME; REVERSIBLE VISUAL-LOSS; SKULL BASE; THICKNESS; AGE; DECOMPRESSION; BONE; RACE; BLINDNESS;
D O I
10.1002/jbmr.4129
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Optic neuropathy (ON) is a highly disabling complication of fibrous dysplasia (FD). The optimal test for identifying and monitoring ON in FD is unknown. Optical coherence tomography (OCT) is an imaging modality that detects retinal nerve fiber layer (RNFL) thinning, a sign of optic nerve atrophy. The purpose of this study was to (i) assess the ability of OCT RNFL thickness measurements to identify ON in FD; (ii) compare the performance of RNFL thickness to computed tomography measurements; and (iii) examine changes in RNFL thickness over time to assess disease progression. A retrospective cohort study was performed to assess subjects (n= 70) who underwent neuro-ophthalmologic examination, including OCT. The diagnostic utility of RNFL thickness was determined using receiver operator characteristic (ROC) curve analysis, and the accuracy was compared with computed tomography measurements. The relationship between RNFL thickness and age was assessed cross-sectionally, using generalized estimating equation methodology, and longitudinally, using a generalized mixed model. Eleven subjects were identified with ON. RNFL thickness identified ON (area under curve = 0.997,p< 0.0001) with sensitivity and specificity of 100% and 95%, respectively, when using the diagnostic criterion of <= 71 mu m. RNFL thickness outperformed computed tomography measurements of optic canal narrowing and optic nerve stretch. Subjects with ON exhibited a greater decrease in RNFL thickness with each year of age (-0.70 mu m/year,p< 0.001) than subjects with normal vision (-0.16 mu m/year,p< 0.05). When assessed longitudinally, subjects with normal vision demonstrated an increase in RNFL thickness until approximately age 20 years that decreased thereafter. In contrast, subjects with ON exhibited an earlier decrease in RNFL thickness during adolescence. In conclusion, RNFL thickness of <= 71 mu m accurately identified ON in this population. By establishing the difference in rate of RNFL thinning in patients with and without ON, clinicians may distinguish between patients at risk for ON and intervene before irreversible damage. (c) 2020 American Society for Bone and Mineral Research.
引用
收藏
页码:2199 / 2210
页数:12
相关论文
共 52 条
[1]   Analysis of Normal Retinal Nerve Fiber Layer Thickness by Age, Sex, and Race Using Spectral Domain Optical Coherence Tomography [J].
Alasil, Tarek ;
Wang, Kaidi ;
Keane, Pearse A. ;
Lee, Hang ;
Baniasadi, Neda ;
de Boer, Johannes F. ;
Chen, Teresa C. .
JOURNAL OF GLAUCOMA, 2013, 22 (07) :532-541
[2]   Optic nerve elongation: Does it exist? [J].
Alvi, A ;
Janecka, IP ;
Kapadia, S ;
Johnson, BL ;
McVay, W .
SKULL BASE SURGERY, 1996, 6 (03) :171-180
[3]   Surgery versus Watchful Waiting in Patients with Craniofacial Fibrous Dysplasia - a Meta-Analysis [J].
Amit, Moran ;
Collins, Michael T. ;
FitzGibbon, Edmond J. ;
Butman, John A. ;
Fliss, Dan M. ;
Gil, Ziv .
PLOS ONE, 2011, 6 (09)
[4]   Ganglion Cell Complex Analysis as a Potential Indicator of Early Neuronal Loss in Idiopathic Intracranial Hypertension [J].
Athappilly, Geetha ;
Garcia-Basterra, Ignacio ;
Machado-Miller, Flavia ;
Hedges, Thomas R. ;
Mendoza-Santiesteban, Carlos ;
Vuong, Laurel .
NEURO-OPHTHALMOLOGY, 2019, 43 (01) :10-17
[5]   Scoliosis in Fibrous Dysplasia/McCune-Albright Syndrome: Factors Associated With Curve Progression and Effects of Bisphosphonates [J].
Berglund, Jason A. ;
Tella, Sri Harsha ;
Tuthill, Kaitlyn F. ;
Kim, Lauren ;
Guthrie, Lori C. ;
Paul, Scott M. ;
Stanton, Robert ;
Collins, Michael T. ;
Boyce, Alison M. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2018, 33 (09) :1641-1648
[6]  
BLAND LI, 1992, ANN OPHTHALMOL, V24, P263
[7]  
Boyce A.M., 1993, GENEREVIEWS
[8]   A Randomized, Double Blind, Placebo-Controlled Trial of Alendronate Treatment for Fibrous Dysplasia of Bone [J].
Boyce, Alison M. ;
Kelly, Marilyn H. ;
Brillante, Beth A. ;
Kushner, Harvey ;
Wientroub, Shlomo ;
Riminucci, Mara ;
Bianco, Paolo ;
Robey, Pamela G. ;
Collins, Michael T. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2014, 99 (11) :4133-4140
[9]   Optic Neuropathy in McCune-Albright Syndrome: Effects of Early Diagnosis and Treatment of Growth Hormone Excess [J].
Boyce, Alison M. ;
Glover, McKinley ;
Kelly, Marilyn H. ;
Brillante, Beth A. ;
Butman, John A. ;
Fitzgibbon, Edmond J. ;
Brewer, Carmen C. ;
Zalewski, Christopher K. ;
Peck, Carolee M. Cutler ;
Kim, H. Jeffrey ;
Collins, Michael T. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 98 (01) :E126-E134
[10]   Optic nerve decompression in fibrous dysplasia: Indications, efficacy, and safety [J].
Chen, YR ;
Breidahl, A ;
Chang, CN .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1997, 99 (01) :22-30