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1.
Int J Mol Sci ; 25(12)2024 Jun 14.
Article de Anglais | MEDLINE | ID: mdl-38928273

RÉSUMÉ

Age-related macular degeneration (AMD) is a chronic disease, which often develops in older people, but this is not the rule. AMD pathogenesis changes include the anatomical and functional complex. As a result of damage, it occurs, in the retina and macula, among other areas. These changes may lead to partial or total loss of vision. This disease can occur in two clinical forms, i.e., dry (progression is slowly and gradually) and exudative (wet, progression is acute and severe), which usually started as dry form. A coexistence of both forms is possible. AMD etiology is not fully understood. Extensive genetic studies have shown that this disease is multifactorial and that genetic determinants, along with environmental and metabolic-functional factors, are important risk factors. This article reviews the impact of heavy metals, macro- and microelements, and genetic factors on the development of AMD. We present the current state of knowledge about the influence of environmental factors and genetic determinants on the progression of AMD in the confrontation with our own research conducted on the Polish population from Kuyavian-Pomeranian and Lubusz Regions. Our research is concentrated on showing how polluted environments of large agglomerations affects the development of AMD. In addition to confirming heavy metal accumulation, the growth of risk of acute phase factors and polymorphism in the genetic material in AMD development, it will also help in the detection of new markers of this disease. This will lead to a better understanding of the etiology of AMD and will help to establish prevention and early treatment.


Sujet(s)
Dégénérescence maculaire , Humains , Dégénérescence maculaire/génétique , Dégénérescence maculaire/étiologie , Facteurs de risque , Prédisposition génétique à une maladie , Métaux lourds/toxicité , Métaux lourds/effets indésirables , Exposition environnementale/effets indésirables , Immunogénétique
2.
Sci Rep ; 14(1): 14788, 2024 06 26.
Article de Anglais | MEDLINE | ID: mdl-38926484

RÉSUMÉ

This study aims to assess the association between nicotine replacement therapy (NRT), varenicline, and untreated smoking with the risk of developing eye disorders. We employed a new-user design to investigate the association between NRT use and the incidence of eye disorders by the Taiwan National Health Insurance program. This study included 8416 smokers who received NRT and 8416 smokers who did not receive NRT (control group) matched using propensity scores between 2007 and 2018. After adjustment for relevant factors, a multivariable Cox regression analysis revealed that compared with untreated smokers, NRT use was associated with a significantly reduced risk of macular degeneration (hazard ratio [HR]: 0.34; 95% confidence interval [CI]: 0.13-0.87, P = 0.024). When stratified by dose, short-term NRT use (8-28 defined daily doses) was associated with significantly lower risk of glaucoma (HR: 0.35; 95% CI: 0.16-0.80, P = 0.012) and a trend toward reduced risk of cataract (HR: 0.60; 95% CI: 0.36-1.01, P = 0.053) compared to no treatment. However, these associations were not observed with long-term NRT use. The results of this real-world observational study indicate that NRT use, particularly short-term use, was associated with a lower risk of certain eye disorders compared to no treatment for smoking cessation. Long-term NRT use did not demonstrate the same benefits. Thus, short-term NRT may be a beneficial treatment strategy for reducing the risk of eye disorders in smokers attempting to quit. However, further evidence is required to verify these findings and determine the optimal duration of NRT use.


Sujet(s)
Cataracte , Glaucome , Dégénérescence maculaire , Arrêter de fumer , Humains , Mâle , Femelle , Glaucome/épidémiologie , Glaucome/étiologie , Adulte d'âge moyen , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Études rétrospectives , Cataracte/épidémiologie , Taïwan/épidémiologie , Sujet âgé , Adulte , Fumer/effets indésirables , Fumer/épidémiologie , Dispositifs de sevrage tabagique , Incidence , Varénicline/usage thérapeutique
3.
FASEB J ; 38(10): e23676, 2024 May 31.
Article de Anglais | MEDLINE | ID: mdl-38783765

RÉSUMÉ

The escalating prevalence of metabolic syndrome poses a significant public health challenge, particularly among aging populations, with metabolic dysfunctions contributing to pro-inflammatory states. In this review, we delved into the less recognized association between hyperuricemia (HUA), a manifestation of metabolic syndrome and a primary risk factor for gout, and age-related macular degeneration (AMD), a sight-threatening ailment predominantly affecting the elderly. In recent years, inflammation, particularly its involvement in complement pathway dysregulation, has gained prominence in AMD pathophysiology. The contradictory role of uric acid (UA) in intercellular and intracellular environments was discussed, highlighting its antioxidant properties in plasma and its pro-oxidant effects intracellularly. Emerging evidence suggests a potential link between elevated serum uric acid levels and choroid neovascularization in AMD, providing insights into the role of HUA in retinal pathologies. Various pathways, including crystal-induced and non-crystal-induced mechanisms, were proposed to indicate the need for further research into the precise molecular interactions. The implication of HUA in AMD underscores its potential involvement in retinal pathologies, which entails interdisciplinary collaboration for a comprehensive understanding of its impact on retina and related clinical manifestations.


Sujet(s)
Goutte , Hyperuricémie , Dégénérescence maculaire , Humains , Hyperuricémie/complications , Hyperuricémie/métabolisme , Dégénérescence maculaire/étiologie , Dégénérescence maculaire/métabolisme , Goutte/métabolisme , Goutte/étiologie , Acide urique/métabolisme , Acide urique/sang , Animaux
4.
Nutrients ; 16(9)2024 Apr 25.
Article de Anglais | MEDLINE | ID: mdl-38732522

RÉSUMÉ

This study assessed the prevalence of myopia, cataracts, glaucoma, and macular degeneration among Koreans over 40, utilizing data from the 7th Korea National Health and Nutrition Examination Survey (KNHANES VII, 2018). We analyzed 204,973 adults (44% men, 56% women; mean age 58.70 ± 10.75 years), exploring the association between myopia and these eye diseases through multivariate logistic regression, adjusting for confounders and calculating adjusted odds ratios (ORs) with 95% confidence intervals (CIs). Results showed a myopia prevalence of 44.6%, cataracts at 19.4%, macular degeneration at 16.2%, and glaucoma at 2.3%, with significant differences across ages and genders. A potential link was found between myopia and an increased risk of cataracts and macular degeneration, but not with glaucoma. Additionally, a higher dietary intake of carbohydrates, polyunsaturated and n-6 fatty acids, vitamins, and minerals correlated with lower risks of these diseases, underscoring the importance of the diet in managing and preventing age-related eye conditions. These findings highlight the need for dietary considerations in public health strategies and confirm myopia as a significant risk factor for specific eye diseases in the aging Korean population.


Sujet(s)
Cataracte , Régime alimentaire , Dégénérescence maculaire , Myopie , Enquêtes nutritionnelles , Humains , Mâle , Femelle , République de Corée/épidémiologie , Adulte d'âge moyen , Études transversales , Myopie/épidémiologie , Myopie/étiologie , Sujet âgé , Prévalence , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Adulte , Facteurs de risque , Cataracte/épidémiologie , Cataracte/étiologie , Régime alimentaire/statistiques et données numériques , Régime alimentaire/effets indésirables , Maladies de l'oeil/épidémiologie , Maladies de l'oeil/étiologie , Glaucome/épidémiologie , Glaucome/étiologie , Odds ratio , Nutriments
5.
Sci Rep ; 14(1): 11016, 2024 05 14.
Article de Anglais | MEDLINE | ID: mdl-38745035

RÉSUMÉ

The aim of this study is to assess the relationship between dietary intake of fatty acids and the age-related macular degeneration (AMD) in the United States population. Adult participants of the 2005-2008 National Health and Nutrition Examination Survey (NHANES) were included in this nationwide cross-sectional study. Dietary fatty acid intake was obtained from two 24-h dietary recall interviews. The intake of dietary fatty acids was analyzed as a continuous and categorical variable. AMD status was assessed using nonmydriatic fundus photographs. Univariate and multivariate logistic regression analyses were used to assess the association between dietary fatty acid intake and AMD. The unweighted population included 4702 individuals of whom 374 had AMD. After adjusting for relevant variables, each 1 unit increase (1 mg/1000 kcal) intake of EPA (OR: 0.996, 95% CI: 0.993-0.996, P = 0.018), DPA (OR: 0.976, 95% CI: 0.962-0.990, P = 0.002), and DHA (OR: 0.996, 95% CI: 0.994-0.999, P = 0.003) were significantly decreased odds of any AMD. The highest versus lowest quartile of EPA (OR: 0.476, P for trend < 0.001), DPA (OR: 0.467, P for trend = 0.005) and DHA (OR: 0.586, P for trend = 0.008) were negatively associated with the odds of any AMD. Subgroup analysis showed that higher quartiles of EPA (OR: 0.461, P for trend < 0.002), DPA (OR: 0.467, P for trend = 0.006) and DHA (OR: 0.578, P for trend = 0.007) exhibited a negative association with early AMD. The study found no significant association between the intake of dietary fatty acids, including n-3 PUFA, and the odds of late AMD. In the 2005-2008 NHANES population, higher dietary DHA, DPA and EPA intake associated with decreased odds of early AMD. However, no clear association was found between specific types of FAs and late AMD.


Sujet(s)
Acides gras , Dégénérescence maculaire , Enquêtes nutritionnelles , Humains , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Études transversales , Acides gras/administration et posologie , États-Unis/épidémiologie , Matières grasses alimentaires/administration et posologie , Adulte , Régime alimentaire , Acide eicosapentanoïque/administration et posologie
6.
Neurobiol Aging ; 140: 41-59, 2024 Aug.
Article de Anglais | MEDLINE | ID: mdl-38723422

RÉSUMÉ

Aging is the main risk factor for age-related macular degeneration (AMD), a retinal neurodegenerative disease that leads to irreversible blindness, particularly in people over 60 years old. Retinal pigmented epithelium (RPE) atrophy is an AMD hallmark. Genome-wide chromatin accessibility, DNA methylation, and gene expression studies of AMD and control RPE demonstrate epigenomic/transcriptomic changes occur during AMD onset and progression. However, mechanisms by which molecular alterations of normal aging impair RPE function and contribute to AMD pathogenesis are unclear. Here, we specifically interrogate the RPE translatome with advanced age and across sexes in a novel RPE reporter mouse model. We find differential age- and sex- associated transcript expression with overrepresentation of pathways related to inflammation in the RPE. Concordant with impaired RPE function, the phenotypic changes in the aged translatome suggest that aged RPE becomes immunologically active, in both males and females, with some sex-specific signatures, which supports the need for sex representation for in vivo studies.


Sujet(s)
Vieillissement , Dégénérescence maculaire , Épithélium pigmentaire de la rétine , Caractères sexuels , Animaux , Épithélium pigmentaire de la rétine/métabolisme , Épithélium pigmentaire de la rétine/anatomopathologie , Femelle , Mâle , Vieillissement/génétique , Vieillissement/physiologie , Vieillissement/anatomopathologie , Dégénérescence maculaire/génétique , Dégénérescence maculaire/anatomopathologie , Dégénérescence maculaire/étiologie , Transcriptome , Modèles animaux de maladie humaine , Expression des gènes , Inflammation , Souris , Souris de lignée C57BL
7.
Hum Cell ; 37(4): 1056-1069, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38744794

RÉSUMÉ

Epithelial mesenchymal transition (EMT) occurring in retinal pigment epithelial cells (RPE) is a crucial mechanism that contributes to the development of age-related macular degeneration (AMD), a pivotal factor leading to permanent vision impairment. Long non-coding RNAs (lncRNAs) have emerged as critical regulators orchestrating EMT in RPE cells. In this study, we explored the function of the lncRNA CYTOR (cytoskeleton regulator RNA) in EMT of RPE cells and its underlying mechanisms. Through weighted correlation network analysis, we identified CYTOR as an EMT-related lncRNA associated with AMD. Experimental validation revealed that CYTOR orchestrates TGF-ß1-induced EMT, as well as proliferation and migration of ARPE-19 cells. Further investigation demonstrated the involvement of CYTOR in regulating the WNT5A/NFAT1 pathway and NFAT1 intranuclear translocation in the ARPE-19 cell EMT model. Mechanistically, CHIP, EMSA and dual luciferase reporter assays confirmed NFAT1's direct binding to CYTOR's promoter, promoting transcription. Reciprocally, CYTOR overexpression promoted NFAT1 expression, while NFAT1 overexpression increased CYTOR transcription. These findings highlight a mutual promotion between CYTOR and NFAT1, forming a positive feedback loop that triggers the EMT phenotype in ARPE-19 cells. These discoveries provide valuable insights into the molecular mechanisms of EMT and its association with AMD, offering potential avenues for targeted therapies in EMT-related conditions, including AMD.


Sujet(s)
Transition épithélio-mésenchymateuse , Rétrocontrôle physiologique , Dégénérescence maculaire , Facteurs de transcription NFATC , ARN long non codant , Épithélium pigmentaire de la rétine , Transition épithélio-mésenchymateuse/génétique , Humains , Épithélium pigmentaire de la rétine/métabolisme , Épithélium pigmentaire de la rétine/cytologie , Facteurs de transcription NFATC/métabolisme , Facteurs de transcription NFATC/génétique , ARN long non codant/physiologie , ARN long non codant/génétique , ARN long non codant/métabolisme , Dégénérescence maculaire/génétique , Dégénérescence maculaire/métabolisme , Dégénérescence maculaire/anatomopathologie , Dégénérescence maculaire/étiologie , Expression des gènes/génétique , Prolifération cellulaire/génétique , Mouvement cellulaire/génétique , Facteur de croissance transformant bêta-1/métabolisme , Transduction du signal/génétique , Transduction du signal/physiologie , Cellules épithéliales/métabolisme , Lignée cellulaire , Cellules cultivées
8.
Sci Total Environ ; 938: 173580, 2024 Aug 15.
Article de Anglais | MEDLINE | ID: mdl-38810762

RÉSUMÉ

BACKGROUND: As the leading cause of blindness, age-related macular degeneration (AMD) performs an adverse impact on human health and disability. AMD have been reported to be associated with environmental factors; however, the association between ultraviolet (UV) radiation, warm-season ambient ozone pollution, and incident AMD remains unclear. METHODS: In this study, 19,707 participants without AMD at baseline were included from a nationwide longitudinal cohort in China. UV radiation and warm-season ozone exposure were evaluated through satellite-based models. Incident AMD was diagnosed via ophthalmological fundus images. Cox proportional hazard regression models were employed to explore the association of UV radiation and warm-season ozone with incident AMD, and the hazard ratios (HRs) and 95 % confidence intervals (CIs) were reported. RESULTS: During 312,935 person-month of follow-up, 3774 participants developed to AMD. High exposure to both UV radiation and warm-season ozone was associated with increasing risk of incident AMD, with HRs and 95 % CIs of 1.32 (1.23, 1.41) and 1.20 (1.11, 1.29) in two-exposure models, respectively. Moreover, negative interaction between UV radiation and warm-season ozone was identified, and it was found that exposure to high UV radiation and low ozone presented the highest hazard for AMD. Subgroup analyses showed that the UV-AMD association was stronger in southern China, while the ozone-AMD association was greater in northern China and rural areas. CONCLUSION: Our study provides the first epidemiological evidence that both UV radiation and warm-season ozone would elevate the risk of incident AMD, and the hazard of higher UV radiation may be attenuated by exposure to ozone. Strategies for decreasing AMD burden should jointly consider environmental exposures and geographic locations.


Sujet(s)
Polluants atmosphériques , Pollution de l'air , Exposition environnementale , Dégénérescence maculaire , Ozone , Rayons ultraviolets , Ozone/analyse , Humains , Chine/épidémiologie , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Pollution de l'air/statistiques et données numériques , Mâle , Femelle , Exposition environnementale/statistiques et données numériques , Sujet âgé , Adulte d'âge moyen , Études de cohortes , Saisons , Incidence
9.
BMC Ophthalmol ; 24(1): 202, 2024 Apr 30.
Article de Anglais | MEDLINE | ID: mdl-38684968

RÉSUMÉ

BACKGROUND: Several epidemiological studies have investigated the association between ambient air pollution and age-related macular degeneration (AMD). However, a consensus has not yet been reached. Our meta-analysis aimed to clarify this association. METHODS: Databases, including PubMed, EMBASE, and Web of Science, were searched for relevant studies from 01 January 2000 to 30 January 2024. English-language, peer-reviewed studies using cross-sectional, prospective, or retrospective cohorts and case-control studies exploring this relationship were included. Two authors independently extracted data and assessed study quality. A random-effects model was used to calculate pooled covariate-adjusted odds ratios. Heterogeneity across studies was also tested. RESULTS: We identified 358 relevant studies, of which eight were included in the meta-analysis. Four studies evaluated the association between particulate matter less than 2.5 µm in diameter (PM2.5) and AMD, and three studies explored the relationship between nitrogen dioxide (NO2) or ozone (O3) and AMD. The pooled odds ratios were 1.16 (95% confidence interval [CI]: 1.11-1.21), 1.17 (95% CI: 1.09-1.25), and 1.06 (95% CI: 1.05-1.07), respectively. CONCLUSION: Current evidence suggests a concomitant positive but not causal relationship between PM2.5, NO2, or O3 and AMD risk.


Sujet(s)
Pollution de l'air , Dégénérescence maculaire , Humains , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Pollution de l'air/effets indésirables , Matière particulaire/effets indésirables , Facteurs de risque , Polluants atmosphériques/effets indésirables , Odds ratio , Ozone/effets indésirables , Dioxyde d'azote/effets indésirables , Dioxyde d'azote/analyse , Exposition environnementale/effets indésirables
11.
Mol Ther ; 32(5): 1445-1460, 2024 May 01.
Article de Anglais | MEDLINE | ID: mdl-38504520

RÉSUMÉ

Age-related macular degeneration (AMD) is the most common cause of untreatable blindness in the developed world. Recently, CDHR1 has been identified as the cause of a subset of AMD that has the appearance of the "dry" form, or geographic atrophy. Biallelic variants in CDHR1-a specialized protocadherin highly expressed in cone and rod photoreceptors-result in blindness from shortened photoreceptor outer segments and progressive photoreceptor cell death. Here we demonstrate long-term morphological, ultrastructural, functional, and behavioral rescue following CDHR1 gene therapy in a relevant murine model, sustained to 23-months after injection. This represents the first demonstration of rescue of a monogenic cadherinopathy in vivo. Moreover, the durability of CDHR1 gene therapy seems to be near complete-with morphological findings of the rescued retina not obviously different from wildtype throughout the lifespan of the mouse model. A follow-on clinical trial in patients with CDHR1-associated retinal degeneration is warranted. Hypomorphic CDHR1 variants may mimic advanced dry AMD. Accurate clinical classification is now critical, as their pathogenesis and treatment are distinct.


Sujet(s)
Protéines apparentées aux cadhérines , Cadhérines , Modèles animaux de maladie humaine , Thérapie génétique , Protéines de tissu nerveux , Cellules photoréceptrices en cône de la rétine , Dégénérescence de la rétine , Cellules photoréceptrices en bâtonnet de la rétine , Animaux , Souris , Cellules photoréceptrices en bâtonnet de la rétine/métabolisme , Cellules photoréceptrices en bâtonnet de la rétine/anatomopathologie , Cellules photoréceptrices en cône de la rétine/métabolisme , Cellules photoréceptrices en cône de la rétine/anatomopathologie , Cadhérines/génétique , Cadhérines/métabolisme , Dégénérescence de la rétine/génétique , Dégénérescence de la rétine/thérapie , Dégénérescence de la rétine/étiologie , Humains , Thérapie génétique/méthodes , Dégénérescence maculaire/thérapie , Dégénérescence maculaire/génétique , Dégénérescence maculaire/anatomopathologie , Dégénérescence maculaire/étiologie , Dégénérescence maculaire/métabolisme
12.
Prog Retin Eye Res ; 101: 101260, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38521386

RÉSUMÉ

People are living longer and rates of age-related diseases such as age-related macular degeneration (AMD) are accelerating, placing enormous burdens on patients and health care systems. The quality of carbohydrate foods consumed by an individual impacts health. The glycemic index (GI) is a kinetic measure of the rate at which glucose arrives in the blood stream after consuming various carbohydrates. Consuming diets that favor slowly digested carbohydrates releases sugar into the bloodstream gradually after consuming a meal (low glycemic index). This is associated with reduced risk for major age-related diseases including AMD, cardiovascular disease, and diabetes. In comparison, consuming the same amounts of different carbohydrates in higher GI diets, releases glucose into the blood rapidly, causing glycative stress as well as accumulation of advanced glycation end products (AGEs). Such AGEs are cytotoxic by virtue of their forming abnormal proteins and protein aggregates, as well as inhibiting proteolytic and other protective pathways that might otherwise selectively recognize and remove toxic species. Using in vitro and animal models of glycative stress, we observed that consuming higher GI diets perturbs metabolism and the microbiome, resulting in a shift to more lipid-rich metabolomic profiles. Interactions between aging, diet, eye phenotypes and physiology were observed. A large body of laboratory animal and human clinical epidemiologic data indicates that consuming lower GI diets, or lower glycemia diets, is protective against features of early AMD (AMDf) in mice and AMD prevalence or AMD progression in humans. Drugs may be optimized to diminish the ravages of higher glycemic diets. Human trials are indicated to determine if AMD progression can be retarded using lower GI diets. Here we summarized the current knowledge regarding the pathological role of glycative stress in retinal dysfunction and how dietary strategies might diminish retinal disease.


Sujet(s)
Produits terminaux de glycation avancée , Dégénérescence maculaire , Humains , Dégénérescence maculaire/étiologie , Animaux , Produits terminaux de glycation avancée/métabolisme , Indice glycémique/physiologie , Glycémie/métabolisme , Hydrates de carbone alimentaires/effets indésirables
13.
BMJ Open ; 14(2): e082471, 2024 Feb 28.
Article de Anglais | MEDLINE | ID: mdl-38418238

RÉSUMÉ

INTRODUCTION: Sickle cell disease (SCD) is one of the most common genetic disorders in the UK, with over 15 000 people affected. Proliferative sickle cell retinopathy (SCR) is a well-described complication of SCD and can result in significant sight loss, although the prevalence in the UK is not currently known. There are currently no national screening guidelines for SCR, with wide variations in the management of the condition across the UK. METHODS AND ANALYSIS: The Sickle Eye Project is an epidemiological, cross-sectional, non-interventional study to determine the prevalence of visual impairment due to SCR and/or maculopathy in the UK. Haematologists in at least 16 geographically dispersed hospitals in the UK linked to participating eye clinics will offer study participation to consecutive patients meeting the inclusion criteria attending the sickle cell clinic. The following study procedures will be performed: (a) best corrected visual acuity with habitual correction and pinhole, (b) dilated slit lamp biomicroscopy and funduscopy, (c) optical coherence tomography (OCT), (d) OCT angiography where available, (e) ultrawide fundus photography, (f) National Eye Institute Visual Function Questionnaire-25 and (g) acceptability of retinal screening questionnaire. The primary outcome is the proportion of people with SCD with visual impairment defined as logarithm of the minimum angle of resolution ≥0.3 in at least one eye. Secondary outcomes include the prevalence of each stage of SCR and presence of maculopathy by age and genotype; correlation of stage of SCR and maculopathy to severity of SCD; the impact of SCR and presence of maculopathy on vision-related quality of life; and the acceptability to patients of routine retinal imaging for SCR and maculopathy. ETHICS AND DISSEMINATION: Ethical approval was obtained from the South Central-Oxford A Research Ethics Committee (REC 23/SC/0363). Findings will be reported through academic journals in ophthalmology and haematology.


Sujet(s)
Drépanocytose , Dégénérescence maculaire , Rétinopathies , Vision faible , Humains , Prévalence , Études transversales , Qualité de vie , Rétinopathies/épidémiologie , Rétinopathies/étiologie , Drépanocytose/complications , Drépanocytose/épidémiologie , Drépanocytose/diagnostic , Dégénérescence maculaire/étiologie , Dégénérescence maculaire/complications , Vision faible/complications , Tomographie par cohérence optique/méthodes , Royaume-Uni/épidémiologie
14.
Ophthalmologica ; 247(2): 73-84, 2024.
Article de Anglais | MEDLINE | ID: mdl-38266500

RÉSUMÉ

BACKGROUND: The aim of this review was to systematically summarize the current knowledge on type 3 macular neovascularization (MNV3) in age-related macular degeneration (AMD). SUMMARY: Recent histopathologic and multimodal imaging findings led to the consensus definition of the new term "type 3 macular neovascularization" in AMD. MNV3 originates in the deep vascular plexus as a neovascular process without connection with the retinal pigment epithelium in the initial stages. This type has numerous clinical and pathomorphologic features that separate it from the other two types of MNV in AMD. Besides, its frequency appears to be higher than previously thought. In optical coherence tomography (OCT), MNV3 can be classified into stages 1-3. Hyperreflective foci in the outer retina possibly represent a precursor lesion. In addition, MNV3 is characterized by a strong association with reticular pseudodrusen, a high rate of bilaterality, close associations with advanced age and arterial hypertension, decreased choroidal thickness, and decreased choriocapillaris flow signals. Data from latest anti-vascular endothelial growth factor studies in MNV3 suggest that the OCT biomarkers in intraretinal and subretinal fluids should be interpreted differently than in the other types. Additionally, data from MNV3 eyes should be analyzed separately, allowing optimal type-specific treatment strategies in the future. KEY MESSAGES: This review highlights the need for accurate characterization of neovascular AMD lesions and an MNV type-specific approach, particularly for MNV3.


Sujet(s)
Angiographie fluorescéinique , Dégénérescence maculaire , Tomographie par cohérence optique , Humains , Angiographie fluorescéinique/méthodes , Fond de l'oeil , Macula/anatomopathologie , Dégénérescence maculaire/diagnostic , Dégénérescence maculaire/complications , Dégénérescence maculaire/étiologie , Épithélium pigmentaire de la rétine/anatomopathologie , Tomographie par cohérence optique/méthodes , Dégénérescence maculaire humide/diagnostic
15.
J Fr Ophtalmol ; 47(2): 104043, 2024 Feb.
Article de Français | MEDLINE | ID: mdl-38241770

RÉSUMÉ

The first intraocular lenses (IOLs) used for cataract surgery transmitted both ultraviolet (UV) radiation and visible light to the retina. Colorless UV-blocking IOLs were introduced and rapidly adopted in the 1980s. Yellow-tinted blue-blocking (also known as blue-filtering) IOLs were marketed in the early 1990s. Blue-blocking IOLs were intended to simulate age-related crystalline lens yellowing to reduce the cyanopsia that some patients experienced after cataract surgery. When blue-filtering IOLs were introduced in North America, however, blue-blocking chromophores were advocated as a way to protect patients from age-related macular degeneration (AMD) despite the lack of evidence that normal environmental light exposure causes AMD. The "blue light hazard" is a term that describes the experimental finding that acute, abnormally intense light exposures are potentially more phototoxic to the retina when short rather than long wavelengths are used. Thus, in brief exposures to intense light sources such as welding arcs, ultraviolet radiation is more hazardous than blue light, which is more hazardous than longer wavelength green or red light. International commissions have cautioned that the blue light hazard does not apply to normal indoor or outdoor light exposures. Nonetheless, the hazard is used for commercial purposes to suggest misleadingly that ambient environmental light can cause acute retinal phototoxicity and increase the risk of AMD. Very large epidemiological studies show that blue-blocking IOLs do not reduce the risk or progression of AMD. Additionally, blue-filtering IOLs or spectacles cannot decrease glare disability, because they decrease image and glare illuminance in the same proportion. Blue light is essential for older adults' scotopic photoreception needed to reduce the risk of nighttime falling and related injuries. It is also critical for circadian photoreception that is essential for good health, sleep and cognitive performance. Unfortunately, age-related pupillary miosis, retinal rod and ganglion cell photoreceptor degeneration and decreased outdoor activity all reduce the amount of healthful blue light available to older adults. Blue-restricting IOLs further reduce the available blue light at a time when older adults need it most. Patients and ophthalmologists are exposed to hypothesis-based advertisements for blue-filtering optical devices that suppress short wavelength light critical for vision in dim lighting and for good physical and mental health. Spectacle and intraocular lens selections should be based on scientific fact, not conjecture. Ideal IOLs should improve photoreception rather than limit it permanently. Practice efficiency, surgical convenience and physician-manufacturer relationships may eliminate a patient's opportunity to choose between colorless blue-transmitting IOLs and yellow-tinted, blue-restricting IOLs. Cataract surgeons ultimately determine whether their patients have the opportunity to make an informed choice about their future photoreception.


Sujet(s)
Cataracte , Lentilles intraoculaires , Dégénérescence maculaire , Humains , Sujet âgé , Rayons ultraviolets/effets indésirables , , Lentilles intraoculaires/effets indésirables , Lumière , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Dégénérescence maculaire/prévention et contrôle , Troubles de la vision
16.
JAMA Netw Open ; 7(1): e2351650, 2024 Jan 02.
Article de Anglais | MEDLINE | ID: mdl-38227312

RÉSUMÉ

Importance: Light pollution's impact on human health is increasingly recognized, but its link to exudative age-related macular degeneration (EAMD) remains unclear. Objective: To investigate the association between exposure to outdoor artificial light at night (OALAN) and the risk of incident EAMD. Design, Setting, and Participants: In this nationwide population-based case-control study, all individuals 50 years or older with newly diagnosed EAMD between January 1, 2010, and December 31, 2011, were identified with reference to the Korean National Health Insurance Service registration program database for rare and intractable diseases. Birth year- and sex-matched controls (with no EAMD diagnosis until 2020) were selected at a 1:30 ratio. Data were acquired from May 1 to December 31, 2021, and analyzed from June 1 to November 30, 2022. Exposures: Mean levels of OALAN at participants' residential addresses during 2008 and 2009 were estimated using time-varying satellite data for a composite view of persistent nighttime illumination at an approximate scale of 1 km2. Main Outcomes and Measures: The hazard ratios (HRs) and 95% CIs of the association between residential OALAN and risk of incident EAMD were determined based on maximum likelihood estimation after adjusting for sociodemographic characteristics, comorbidities, and area-level risk factors (ie, nighttime traffic noise and particulate matter of aerodynamic diameter ≤10 µm in each participant's administrative district of residence). Results: A total of 126 418 participants were included in the analysis (mean [SD] age, 66.0 [7.9] years; 78 244 men [61.9%]). Of these, 4078 were patients with newly diagnosed EAMD and 122 340 were EAMD-free matched controls. In fully adjusted models, an IQR (55.8 nW/cm2/sr) increase in OALAN level was associated with an HR of 1.67 (95% CI, 1.56-1.78) for incident EAMD. The exposure-response curve demonstrated a nonlinear, concave upward slope becoming more pronounced at higher levels of light exposure (ie, at approximately 110 nW/cm2/sr). In a subgroup analysis, an IQR increase in OALAN was associated with increased risk of incident EAMD in urban areas (HR, 1.46 [95% CI, 1.33-1.61]) but not in rural areas (HR, 1.01 [95% CI, 0.84-1.22]). Conclusions and Relevance: In this nationwide population-based case-control study, higher levels of residential OALAN were associated with an increased risk of incident EAMD. Future studies with more detailed information on exposure, individual adaptive behaviors, and potential mediators are warranted.


Sujet(s)
Éclairage , Dégénérescence maculaire , Sujet âgé , Humains , Mâle , Études cas-témoins , Bases de données factuelles , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , République de Corée , Éclairage/effets indésirables
17.
JAMA ; 331(2): 147-157, 2024 01 09.
Article de Anglais | MEDLINE | ID: mdl-38193957

RÉSUMÉ

Importance: Age-related macular degeneration (AMD) affects approximately 20 million people in the US and 196 million people worldwide. AMD is a leading cause of severe vision impairment in older people and is expected to affect approximately 288 million people worldwide by 2040. Observations: Older age, genetic factors, and environmental factors, such as cigarette smoking, are associated with development of AMD. AMD occurs when extracellular deposits accumulate in the outer retina, ultimately leading to photoreceptor degeneration and loss of central vision. The late stages of AMD are characterized by outer retinal atrophy, termed geographic atrophy, or neovascularization associated with subretinal and/or intraretinal exudation, termed exudative neovascular AMD. The annual incidence of AMD ranges from 0.3 per 1000 in people who are aged 55 to 59 years to 36.7 per 1000 in people aged 90 years or older. The estimated heritability of late-stage AMD is approximately 71% (95% CI, 18%-88%). Long-term prospective cohort studies show a significantly higher AMD incidence in people who smoke more than 20 cigarettes per day compared with people who never smoked. AMD is diagnosed primarily with clinical examination that includes a special lens that focuses light of the slit lamp through the pupil. Exudative neovascular AMD is best identified using angiography and by optical coherence tomography. Individuals with AMD who take nutritional supplements consisting of high-dose vitamin C, vitamin E, carotenoids, and zinc have a 20% probability to progress to late-stage AMD at 5 years vs a 28% probability for those taking a placebo. In exudative neovascular AMD, 94.6% of patients receiving monthly intravitreal anti-vascular endothelial growth factor (anti-VEGF) injections experience less than a 15-letter visual acuity loss after 12 months compared with 62.2% receiving sham treatment. Conclusions and Relevance: The prevalence of AMD is anticipated to increase worldwide to 288 million individuals by 2040. Intravitreally administered anti-VEGF treatment is first-line therapy for exudative neovascular AMD.


Sujet(s)
Inhibiteurs de l'angiogenèse , Dégénérescence maculaire , Sujet âgé , Sujet âgé de 80 ans ou plus , Humains , Adulte d'âge moyen , Inhibiteurs de l'angiogenèse/administration et posologie , Inhibiteurs de l'angiogenèse/pharmacologie , Inhibiteurs de l'angiogenèse/usage thérapeutique , Injections intravitréennes , Dégénérescence maculaire/diagnostic , Dégénérescence maculaire/traitement médicamenteux , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Études prospectives , Rétine/effets des médicaments et des substances chimiques , Rétine/anatomopathologie , Facteur de croissance endothéliale vasculaire de type A/antagonistes et inhibiteurs , Acuité visuelle , Dégénérescence maculaire humide/diagnostic , Dégénérescence maculaire humide/traitement médicamenteux , Dégénérescence maculaire humide/épidémiologie
18.
Retina ; 44(3): 475-486, 2024 Mar 01.
Article de Anglais | MEDLINE | ID: mdl-37973043

RÉSUMÉ

PURPOSE: To investigate the prevalence and risk factors of age-related macular degeneration features among pilots of Republic of Korea Air Force. METHODS: This retrospective, cross-sectional study was performed with a total of 2781 Republic of Korea Air Force pilots who underwent regular medical examinations between 2020 and 2021. Age-related macular degeneration features were determined and graded by fundus photographs. Risk factors were identified with logistic regression analysis in odds ratio (OR) and 95% confidence interval (CI). RESULTS: The prevalence was 12.9% in the Republic of Korea Air Force pilots and 35.2% in those older than 50 years. Pilots with age-related macular degeneration features were positively associated with age (OR: 1.082, CI: 1.067-1.096, P < 0.001), male sex (OR: 0.229, CI: 0.056-0.939, P = 0.041), smoking (OR: 1.027, CI: 1.008-1.047, P = 0.006), flight time (OR: 1.004, CI: 1.003-1.005, P < 0.001), total cholesterol (OR: 1.004, CI: 1.000-1.007, P = 0.033), and low-density lipoprotein (OR: 1.005, CI: 1.001-1.008, P = 0.011). Aircraft type was also identified as a risk factor (OR: 0.617, CI: 0.460-0.827 for carrier, OR: 0.572, CI: 0.348-0.940 for helicopter, P = 0.002), with fighter pilots having a higher risk than carrier and helicopter pilots. The results were similar for pilots older than 50 years. CONCLUSION: The prevalence of age-related macular degeneration features in Republic of Korea Air Force pilots was higher than in other general populations studied. Identified risk factors such as flight time and aircraft type suggest potential occupational risk of age-related macular degeneration in aviators.


Sujet(s)
Dégénérescence maculaire , Humains , Mâle , Prévalence , Études transversales , Études rétrospectives , Dégénérescence maculaire/diagnostic , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie , Facteurs de risque
20.
Retina ; 44(1): 28-36, 2024 Jan 01.
Article de Anglais | MEDLINE | ID: mdl-38117581

RÉSUMÉ

PURPOSE: To investigate the link between lifelong exposure to ultraviolet radiation (UVR) and the development of age-related macular degeneration (AMD). METHODS: The Alienor study is a prospective population-based cohort involving 963 residents of Bordeaux, France, older than 73 years. A subset of 614 participants for advanced AMD and 422 participants for early AMD were included in the analysis. The participants' residential history combined with UVR estimates from the EuroSun satellite were used to estimate the amount of ambient UVR they have been exposed to over their lifetime. Age-related macular degeneration was classified from retinal fundus photographs and spectral domain optical coherence tomography at 2 to 3 years intervals over the 2006 to 2017 period. Associations between cumulative exposure to ultraviolet A, ultraviolet B, and total (total UV) and the incidence of early and advanced AMD were estimated using multivariate Cox models. RESULTS: Intermediate quartiles of total UV, ultraviolet A, and ultraviolet B exposures were associated with a higher risk for incident early AMD (Hazard Ratio [HR] =2.01 [95% confidence interval [CI] = 1.27-3.13], HR = 2.20 [95% CI = 1.38-3.50], HR = 1.79 [95% CI = 1.13-2.80], respectively) as compared with the lower quartile. However, this risk did not further increase in the highest quartiles of exposure. None of the three types of UVR exposure was significantly associated with incident advanced AMD. CONCLUSION: Despite an increased risk with intermediate compared with low UVR exposure, our study cannot confirm a dose-response relationship of UVR exposure with early AMD onset.


Sujet(s)
Dégénérescence maculaire , Rayons ultraviolets , Humains , Enfant d'âge préscolaire , Incidence , Rayons ultraviolets/effets indésirables , Études prospectives , Facteurs de risque , Dégénérescence maculaire/diagnostic , Dégénérescence maculaire/épidémiologie , Dégénérescence maculaire/étiologie
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