Lagrou Lisa M, Gilbert Jesse, Hannibal Mark, Caird Michelle S, Thomas Inas, Moroi Sayoko E, Bohnsack Brenda L
Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan.
Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan.
J AAPOS. 2018 Jun;22(3):183-187.e1. doi: 10.1016/j.jaapos.2017.12.015. Epub 2018 Apr 7.
To evaluate biomechanical corneal properties in children with osteogenesis imperfecta (OI).
A prospective, observational, case-control study was conducted on children 6-19 years of age diagnosed with OI. Patients with OI and healthy control subjects underwent complete ophthalmic examinations. Additional tests included Ocular Response Analyzer (ORA) and ultrasonic pachymetry. Primary outcomes were central corneal thickness (CCT), corneal hysteresis (CH), and corneal resistance factor (CRF). Intraocular pressure (IOP) was measured directly by either iCare or Goldmann applanation and indirectly by the ORA (Goldmann-correlated and corneal-compensated IOP). Statistically significant differences between OI and control groups were determined using independent samples t test.
A total of 10 of 18 OI cases (mean age, 13 ± 4.37 years; 8 males) and 30 controls (mean age, 12.76 ± 2.62 years; 16 males) were able to complete the corneal biomechanics and pachymetry testing. Children with OI had decreased CH (8.5 ± 1.0 mm Hg vs 11.6 ± 1.2 mm Hg [P < 0.001]), CRF (9.0 ± 1.9 mm Hg vs 11.5 ± 1.5 [P < 0.001]) and CCT (449.8 ± 30.8 μm vs 568 ± 47.6 μm [P < 0.001]) compared to controls. The corneal-compensated IOP was significantly higher in OI cases (18.8 ± 3.1 mm Hg) than in controls (15.0 ± 1.6 mm Hg, P < 0.004), but there was no significant difference in Goldmann-correlated IOP (16.3 ± 4.2 mm Hg vs 15.8 ± 2.2 mm Hg).
Collagen defects in OI alter corneal structure and biomechanics. Children with OI have decreased CH, CRF, and CCT, resulting in IOPs that are likely higher than measured by tonometry. These corneal alterations are present at a young age in OI. Affected individuals should be routinely screened for glaucoma and corneal pathologies.
评估成骨不全症(OI)患儿的角膜生物力学特性。
对6至19岁诊断为OI的患儿进行了一项前瞻性、观察性病例对照研究。OI患者和健康对照受试者均接受了全面的眼科检查。额外的检查包括眼反应分析仪(ORA)和超声测厚法。主要观察指标为中央角膜厚度(CCT)、角膜滞后量(CH)和角膜阻力因子(CRF)。眼压(IOP)通过iCare或Goldmann压平眼压计直接测量,并通过ORA间接测量(Goldmann相关眼压和角膜补偿眼压)。使用独立样本t检验确定OI组和对照组之间的统计学显著差异。
18例OI病例中的10例(平均年龄13±4.37岁;8例男性)和30例对照(平均年龄12.76±2.62岁;16例男性)能够完成角膜生物力学和测厚测试。与对照组相比,OI患儿的CH(8.5±1.0 mmHg对11.6±1.2 mmHg [P<0.001])、CRF(9.0±1.9 mmHg对11.5±1.5 [P<0.001])和CCT(449.8±30.8μm对568±47.6μm [P<0.001])均降低。OI病例的角膜补偿眼压(18.8±3.1 mmHg)显著高于对照组(15.0±1.6 mmHg,P<0.004),但Goldmann相关眼压无显著差异(16.3±4.2 mmHg对15.8±2.2 mmHg)。
OI中的胶原蛋白缺陷会改变角膜结构和生物力学。OI患儿的CH、CRF和CCT降低,导致眼压可能高于眼压计测量值。这些角膜改变在OI患儿中出现较早。受影响个体应常规筛查青光眼和角膜病变。