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Table of Content

    22 October 2020, Volume 44 Issue 5
    The history of elimination of blinding trachoma in China
    Hu Ailian, Wang Ningli
    2020, 44(5):  289-295.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.001
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    Trachoma was the leading blinding eye disease in China. With the unremitting efforts of several generations, it was finally eliminated. The discovery of chlamydia trachomatis provided the scientific basis for the prevention and control of trachoma. In the 70 years since the founding of the People's Republic of China, during trachoma prevention and control process,with comprehensive prevention and control measures including  the prioritization by chinese government, long-term effects in the improvement of water and toilet hygiene and environmental sanitation, increased investment in primary medical care, continuous construction of the three-tier medical service network, expanded coverage of the new rural cooperative medical system, greatly increased accessibility of medical services and availability of medications,  the elimination of blinding trachoma was ultimately achieved.This paper reviews the history of trachoma prevention and control in China, including trachoma epidemic period (before the founding of the People's Republic of China), discovery of chlamydia trachomatis and comprehensive and effective prevention and control of trachoma (after the founding of the People's Republic of China and before the reform and opening up), effective control of trachoma (after reform and opening up to 1999), and elimination of blinding trachoma (after 2000). (Int Rev Ophthalmol, 2020, 44: 289-295)
    Research progress on congenital nystagmus
    Liu Yanzi, Shi Xuefeng
    2020, 44(5):  296-305.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.002
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    Congenital nystagmus (CN) is an involuntary, rhythmic ocular oscillations that is often detected at birth or within 3 months of birth. The etiology of CN is complex and diverse. Till now, the pathogenesis of CN has not been entirely clear. CN is a difficult disease in the clinic of pediatric ophthalmology and strabismus, its treatment is difficult. In recent years, researchers have tried to improve the original surgical procedures in order to give patients better visual quality. Randomized, controlled, double-blind clinical studies have found that some drugs can reduce nystagmus intensity, prolong foveal fixation, and improve vision in patients. The genetic modes of CN are varied, and the pathogenesis of most of the CN is still unclear. Studies on model animals have revealed that the mechanism by which the FRMD7 gene, one of the pathogenic genes of X-linked CN,  is related to the loss of horizontal motion detection of direction selective retinal ganglion cells. This article reviews the recent progress research of CN in order to provide references for future clinical and basic studies. (Int Rev Ophthalmol, 2020, 44:  296-305)
    Intraoperative optical coherence tomography in anterior segment surgery
    Ma Zhongxu
    2020, 44(5):  306-312.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.003
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    Intraoperative optical coherence tomography (iOCT) enables real-time visualization of ocular structures during surgery and provides a dynamic view of the surgical process and instrument-tissue interactions to enhance our understanding of the surgical process, facilitate decision making at crucial steps of surgery, and optimize outcomes. At present, the applications of iOCT in anterior segment are continually expanding, whether hand-held or microscope integrated, and increasingly emerging as a useful adjunct in phacoemulsification, keratoplasty, glaucoma surgeries. It assumes both diagnostic and therapeutic importance in pediatric cases where pre-operative assessment is often not feasible. Otherwise,the applications of iOCT in refractive surgeries and ocular surface disorders is increasingly being evaluated. The limitations of present-day iOCT systems are related to instrument compatibility, automated tracking of the surgical field, and on-table volumetric analysis of the real-time images.(Int Rev Ophthalmol, 2020, 44: 306-312)
    Advances in related mechanisms of intense pulsed light therapy in ocular surface diseases
    Dong Wenhui, Yan Xiaoming
    2020, 44(5):  313-317.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.004
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    The ocular surface indications of intense pulse light therapy have been extended to six diseases such as meibomian gland dysfunction, and the mechanism of intense pulsed light treatment is mainly based on the two major theories of selective photothermatology and photobiomodulation. In addition to photopyrolysis target substrates, photobiomodulation plays an increasingly essential role as one of the important mechanisms of intense pulsed light. Intense pulsed light can not only improve ocular surface symptoms in a short-term, but also has a cumulative treatment efficacy to promote meibomian gland resuscitation.(Int Rev Ophthalmol, 2020, 44:  313-317)

     

    New progress of ocular signal transduction in the pathogenesis of myopia
    Xu Yushan, Zhang Fengju
    2020, 44(5):  318-323.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.005
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    With the increasing prevalence of myopia in China, many studies have been done to explore the pathogenesis of myopia to prevent and treat myopia effectively. Previous studies have shown that the abnormal visual stimulation of myopia is detected by retinal neurons, which generates signals through RPE and choroid into sclera, resulting in scleral remodeling and axial elongation. However, it is not clear how signals are transducted from retina to sclera. Studies have found that TGF-β/Smad, JAK/STAT, retinoic acid, PPAR, Wnt/β-catenin, dopamine, acetylcholine receptor and GABA signaling pathways play an important role in transduction, the study of which has significant clinical value in the prevention and treatment of myopia. (Int Rev Ophthalmol, 2020, 44:  318-323)
    Advances in etiologies and management of congenital hereditary endothelial dystrophy
    Qiu Yingping, Bi Yanlong
    2020, 44(5):  324-330.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.006
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    Congenital hereditary endothelial dystrophy (CHED) is a rare autosomal recessive disorder of the corneal endothelium characterized by nonprogressive bilateral corneal edema and opacification present at birth or shortly thereafter. The role of SLC4A11 in the pathogenesis of CHED has been one of highlights and difficulties in recent years. In addition to SLC4A11, other potential pathogenic genes for CHED, such as MPDZ, should also be considered. Understanding the role of SLC4A11 and other potential pathogenic genes in the pathogenesis of CHED is an important research direction in the future. At present, the only definitive treatment for corneal endothelial dysfunction is corneal transplantation.  Transplantation of tissue-engineered corneal endothelial cells and the use of Rho-associated kinase inhibition has become a positive way to expand the source of donor tissue, which has a certain application prospect in the treatment of CHED. With the development of molecular genetics and pathophysiology of CHED, it is possible that individualized non-surgical treatment with lower trauma and lower cost will realize early intervention of CHED and become the main treatment direction of CHED in the future. Non-steroidal anti-inflammatory drug, engineered SLC4A11-EL3-containing protein and drugs promoting mitochondrial ROS clearance may be effective for different patients, but further verification is needed. It is also very important to screen suitable patients for different treatment methods. (Int Rev Ophthalmol, 2020, 44:324-330)

    Drug therapy of dry eye
    Zhao Lu, Pan Zhiqiang
    2020, 44(5):  331-339.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.007
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    Dry eye is a multifactorial disease characterized by tear hyperosmotic and ocular surface inflammation. Complex pathogenesis and recurrent attacks are the main features of it. Recent studies have proposed that immune reaction and neurosensory abnormalities are also involved in its pathogenesis. With the continuous exploration of its etiology and pathogenesis, the treatment methods are also constantly improving. The traditional medical treatments consist of physical therapy, pharmaceutical and surgery, in which drug plays an important role.  According to etiology and pathogenesis of dry eye, the drugs of it are classified into two categories. One is to improve the quality and stability of tear film, including tear substitutes (such as autologous serum, vitamins and artificial tear complemented with aqueous solution, mucin and lipid), secretagogues (such as aqueous and mucous secretion stimulants) and omega-3 fatty acid supplements. Secondly, more effective, ophthalmic pharmacological drugs targeting various distinct etiology of dry eye have been investigated in improving the ocular surface microenvironment. The corresponding drugs include glucocorticoid eyedrops, non-steroidal anti-inflammatory drugs, immunosuppressants, adhesion factor inhibitors, other treatments in new anti-inflammatory models, antibiotics, reconstruction of microecological balance, antioxidants, neuroprotectants and so on.(Int Rev Ophthalmol, 2020, 44:331-339)

    Application of fundus fluorescein angiography on retinopathy of prematurity
    Wu Lei, Li Manhong, Zhang Zifeng, Wang Yusheng
    2020, 44(5):  340-345.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.008
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    Retinopathy of prematurity (ROP) is the leading cause of childhood blindness worldwide. The clinical fundus examination by indirect ophthalmoscopy and wide-field digital pediatric retinal imaging system is mainly used in ROP screening and management nowadays. The fundus fluorescein angiography (FFA) designed for pediatric patients can provide more useful information regarding retinal and choroidal vasculature in the development and treatment of ROP. FFA has been shown to be critical in ROP diagnosis, treatment guidance, efficacy evaluation, and follow-up. It contributes to the body of ROP knowledge, and will continue to have an evolving role in the prevention and management of ROP. (Int Rev Ophthalmol, 2020, 44:340-345)

    Ozurdex in the treatment of macular edema caused by posterior ophthalmic diseases
    Tan Cong, Qin Mei
    2020, 44(5):  346-350.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.009
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    Macular edema is one of the main causes of visual dysfunction in patients with fundus disease. Many factors cause the destruction of blood-retinal barrier and form macular edema, among which inflammation plays an important role in the formation of macular edema. In order to overcome the limitations of traditional intravitreous hormone injection, dexamethasone vitreous implant (Ozurdex) came into being. Its good clinical effect and unique drug delivery system provide a new choice for the treatment of macular edema. Ozurdex has good efficacy and safety in the theatment of macular edema caused by fundus diseases such as retinal vein occlusion, diabetic retinopathy and non-infective uveitis.(Int Rev Ophthalmol, 2020, 44:346-350)

    Application of OCTA on diagnosis and treatment of retinal vascular diseases
    Linghu Minli, Huang Xionggao
    2020, 44(5):  351-357.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.010
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    【Abstract】As a new fundus vessel examination technology, optical coherence tomography angiography (OCTA) has the advantages of non-invasiveness, swiftness, high resolution and 3D imaging etc. It doesn’t require contrast agent and can clearly and intuitively display the form of the layers of retinal vessels. It has been widely applied in the diagnosis, treatment and analysis of diabetic retinopathy, retinal vein occlusion, choroidal neovascularization, polypoidal choroidal vasculopathy, macular telangiectasia, central serous chorioretinopathy etc. (Int Rev Ophthalmol, 2020, 44:351-357)

    Medical treatment of glaucoma in pregnancy
    Wang Bingsong, Wang Tao
    2020, 44(5):  358-362.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.011
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    In recent years, more women are conceiving at older ages and the treatment of glaucoma in pregnancy is an unique challenge faced by more and more glaucoma specialists. The treatment needs consideration of balancing the effective control of the progress of glaucoma to the mother as against the potential harm to the fetus.  Most of the available researches of glaucoma medication in pregnancy were based on individual case reports or animal experiments. Although at present there is no strong evidence to verify that anti-glaucoma drug is safe for the fetus, if we carefully select appropriate anti-glaucoma drugs and pay attention to the drug administration method, we can help the glaucoma patients and the fetus pass the pregnancy as safely as possible. (Int Rev Ophthalmol, 2020, 44:  358-362)

    Monokine induced by interferon-γ and thyroid associated ophthalmopathy
    Tong Fei, Chen Xinxin, Mou Pei, Wei Ruili
    2020, 44(5):  362-365.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.012
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    Monokine induced by interferon-γ(MIG)is a T-cell chemotactic factor induced by interferon-γ. In many specific autoimmune diseases, MIG is highly expressed in tissue and in serum. In patients with thyroid associated ophthalmopathy (TAO), under the combined influence of IFN-γ and TNF-α, the high level of MIG is secreted by orbital fibroblasts (OFs) and preadipocytes. The activity of TAO is related to the existence of circulating MIG, and the activity of orbital inflammation can be reflected at least in part by the increase of MIG concentration. During corticosteroid, MIG levels decreased significantly compared with baseline values in control and TAO patients. As the specific pathogenesis of TAO is not clear, it is necessary to continue to study the interaction between chemokines and cytokines in the pathogenesis of TAO.(Int Rev Ophthalmol, 2020, 44:  362-365)

    Progress on degradation mechanisms of ubiquitinated proteins in ophthalmic diseases
    Chen Xiaojuan, Zhang Guowei, Qin Miaomiao, Guan Huaijin
    2020, 44(5):  366-372.  doi:10.3760/ cma.j.issn.1673-5803.2020.05.013
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    Ubiquitination is the process by which ubiquitin is covalently attached to substrate proteins through multistage enzymatic reactions. When the aggregated ubiquitinated proteins are overloaded and cannot be cleaned up in time, the health and viability of cells will be threatened. However, the ubiquitination and degradation of some key proteins may cause related diseases. In this review, we summarize the research progress on the degradation mechanisms of ubiquitinated proteins in ophthalmic diseases, in order to provide new ideas and strategies for clinical diagnosis and treatment.(Int Rev Ophthalmol, 2020, 44:366-372)