FormalPara Key Summary Points

Why carry out this study?

Limited research has been conducted on geriatric chronic central serous chorioretinopathy, resulting in a lack of understanding regarding its clinical characteristics and disease progression.

This study aims to explore the potential differences in imaging features and prognosis between older and younger patients with chronic chorioretinopathy (cCSC).

What was learned from the study?

Elderly patients with central chronic serous chorioretinopathy may experience different disease outcomes.

Elderly cCSC patients exhibit less gender bias, poorer vision, more severe structural damage and ischemia in the choroid and retina and have a higher risk of develo** choroidal neovascularization.

Introduction

Central serous chorioretinopathy (CSC) is a disease characterized by the detachment of the retina, with or without detachment of the retinal pigment epithelium (PED). This condition is associated with increased permeability in the choroid and dysfunction of the retinal pigment epithelium [1, 2]. CSC typically presents with varying degrees of visual loss or blurred vision, distortion, diminution of vision, and changes in color vision [3]. The diagnosis of CSC usually involves the use of fluorescein angiography (FFA) and indocyanine green angiography (ICGA), which are considered the gold standard. FFA reveals one or more leakage points at the level of the retinal pigment epithelium, while ICGA shows increased volume, permeability, and delayed filling of choroidal capillaries in multiple regions [4,5,6]. However, the invasive nature of FFA and ICGA limits their widespread use. Non-invasive imaging techniques such as SD-OCT and subsequent SS-OCT have made it possible to observe the retina, choroid, and even the sclera [7]. Previous studies have demonstrated that CSC patients exhibit significantly increased choroidal thickness, expanded large and middle choroidal vessels, attenuated choroidal capillaries, and abnormal retinal perfusion compared to normal controls [8,9,10].

CSC affects predominantly middle-aged people (30 to 50 years old) with a mean age of onset around 40 years old (39 to 41 years) and has a significant male preference [11,12,13]. The incidence rate of senile CSC is low, and it is easy to be complicated with choroidal neovascularization. Its clinical manifestations are very different from those of young CSC patients, and it is easy to confuse age-related macular degeneration (AMD) and polypoid choroidal vasculopathy (PCV), which makes the diagnosis of elderly CSC patients difficult [14, 15]. The number of elderly CSC patients seems to be increasing due to the aging population and the development of multimodal imaging. However, we know little about the unique pathological changes and clinical manifestations of elderly CSC patients.

Our purpose is to investigate the characteristic changes of retina, choroid structure, and blood flow in elderly patients with cCSC using scanning laser fundus color photography, FFA, ICGA, SS-OCT, SS-OCTA, and other imaging technologies, explore the unique clinical characteristics them and reveal new information about its pathogenesis.

Methods

This retrospective study was approved by the Ethics Committee of the First Affiliated Hospital of Zhengzhou University, and all research and data collection complied with the Declaration of Helsinki. Patients were informed of the risks of invasive examinations and signed informed consent forms.

Newly diagnosed treatment-naïve chronic CSC patients were included in this study from June 2021 to January 2023 at the First Affiliated Hospital of Zhengzhou University. They were divided into two groups according to age: the young group (aged between 20 and 50 years old), 45 men with 47 eyes and 13 women with 15 eyes; the elderly group (age ≥ 50 years old), 18 males with 20 eyes and 14 females with 17 eyes. Among the young group, no complications were observed. However, in the elderly group, seven patients had comorbidities of hypertension, three patients had comorbidities of diabetes, and two patients had comorbidities of lower limb varicose veins. At the same time, we recruited 40 age- and sex-matched normal controls (40 eyes), all of whom were included in the right eye data for statistical analysis.

Chronic central serous chorioretinopathy was diagnosed as a neurosensory detachment resulting from one or more sites of leakage at the level of the retinal pigment epithelium (RPE) during the initial clinical examination. Additionally, there was evidence of persistent subretinal fluid (SRF) lasting for a duration of 3 months or longer. PCV can be ruled out by the presence of polypoidal lesions on SS-OCT B-scan images or ICGA. AMD can be ruled out by evaluating choroidal thickness and leakage pattern on FFA. Exclusion criteria include: (1) other retinal or choroidal diseases those can cause SRF; (2) the patient has a history of laser photocoagulation or other eye surgery; (3) choroidal neovascularization (CNV) was detected by OCT angiography (OCTA) or FFA; (4) poor image quality cannot be accurately analyzed; (5) high myopia, equivalent spherical lens > — 6D or eye axis > 26 mm.

All CSC patients received complete ophthalmic examination, including optometry, intraocular pressure measurement, slit lamp biomicroscope, scanning laser fundus color photography, FFA, SS-OCT, SS-OCTA (SS-OCTA, VG200D, micro-image, Luoyang, China), and some patients received ICGA examination. The OCT instrument VG-200 used in this study is equipped with a scanning laser with a central wavelength of 1050 nm, with a scanning speed of 200000A-Scans/s, axial resolution of 1.8 µm, and scanning depth of 6 mm. All the eyes examined were centered on the fovea of the macula, and the images were obtained by using Angio 6 mm × 6 mm 512 × 512 R4 and Star 18Line R16 scanning modes. The choroid is defined as the area from the base boundary of RPE-Bruch membrane complex to the junction of choroid and sclera. Except FFA and ICGA, healthy subjects received the same ophthalmic examination as CSC patients.

In this study, we recorded the demographic and basic clinical characteristics of cCSC patients at the time of treatment, such as age, sex, eye type, equivalent spherical lens degree, BCVA (expressed in logarithm of the equivalent value of the minimum resolution angle (logMAR). According to SS-OCT b-scan images, determine whether there are ruptured ellipsoid zone (EZ-), subfoveal fibrin in SRF, pachydrusen, subretinal drusenoid deposits (SDD), pigment epithelial detachment (PED, defined as dome-shaped detachment of the pigment epithelium from Bruchx’s membrane), double layer sign (DLS, defined as the detachment of RPE from the shallow irregular elevation of irregularly pigmented epithelium on Bruch's membrane), choroidal lipid globule cavern (choroidal lipid globule cavern is defined as the appearance of choroidal void, focal ellipsoid low reflection area in the Sattler and Haller layers, with a high penetration imaging trail behind, and no blood flow signal in OCTA [22, 30, 31]. Some studies have shown that the presence of fibrin in subretinal fluid is related to the serious damage of RPE and poor visual acuity [32]. The incidence of fibrin in our cohort is significantly higher in the elderly group.

Drusen are deposits of yellow-white extracellular debris composed of complement protein, esterified and non-esterified cholesterol, apolipoprotein, carbohydrate and trace elements, which are located above the retinal pigment epithelium (RPE) or between RPE and Bruch membrane. Soft glass verruca and reticular pseudovitreous verruca (also known as verruciform sediment SDD) are considered as typical pathological changes of age-related age degeneration (AMD) [33, 34]. Rick Spaide reported in 2018 that pachydrusen, a special entity, was isolated, with a diameter greater than 125 μm. It is related to choroidal thickening in non-exudative macular degeneration [35]. Hidetaka et al. [36] studied 302 eyes with CSC and found that the incidence of pachydrusen in CSC was 27.2%, and often located in the delayed area of choroidal capillary filling and above the dilated choroidal vessels. Kihwang et al. [37] concluded that the attenuation of choroidal capillaries was the main reason for the occurrence of pachydrusen and found that the incidence of pachydrusen in cCSC was closely related to age. In this study, we found that the probability of pachydrusen and SDD was significantly higher in the elderly group than in the younger group, but no soft drusen was found in either group. Also, the choroidal capillary perfusion area was markedly lower in the elderly group than that in the young group, supporting the above view. Jay et al. [38] believed that pachydrusen might be a potential risk factor for the development of PCD. When the eyes with pachydrusen developed macular neovascularization (MNV), the main manifestation was PCV [39]. The incidence of SDD in our cohort is very low and only found in the elderly group. It is reported that the incidence of SDD in PCV is 4.1%, which is considered as an independent risk factor for neovascularization [40], while the incidence of pachydrusen in PCV is 70% [41]. We believe that elderly cCSC patients with hyaline warts are more likely to develop PCV. In the next study, we will perform a longitudinal observation of elderly cCSC patients with hyaline to validate our view.

Friedman and Smith [42] first described the existence of choroidal lipid globule cavern in human eyes after death. Rosa et al. [43] used OCT to observe the focal ellipsoid low reflection area at the choroidal level in patients with AMD map-like atrophy, followed by a high penetration imaging trail. There was no blood flow signal in OCTA, and it was proved from the histology that the low reflection area was lipid droplets. Subsequently, some studies showed that in about 52% of eyes with thick choroidal membranes there are lipid granular cavities. Compared with the normal control and AMD patients, cCSC patients had a greater size and number of lipid grain-like cavities patients, and more cavities appeared in the area of increased choroidal vascular permeability, which was associated with increased choroidal thickness and the loss of choroidal stroma [17]. The incidence of choroidal lipid globule cavern in both groups was 56.76 and 50.82%, respectively, suggesting that choroidal matrix loss and lipidation in cCSC patients also explain, to some extent the decrease in choroidal thickness in the elderly group. The increase in lipid-like cavities means the increase in extracellular lipid deposition, which is involved in the process of choroidal oxidative stress. However, histology shows no evidence of inflammatory cells in the vicinity of the lipid droplets [43]. The prognostic significance of lipid-like cavities on cCSC still needs further study.

The nutrients of outer layer of retina (outer nuclear layer, photoreceptor layers and retinal pigment epithelial layer) is mainly supplied by choroidal capillary [44], and nutrients of the middle layer of retina (inner core layer and inner subordinate layer) and inner layer (nerve fiber layer and ganglion cell layer) are supplied by retinal capillary [45]. Vascular dilation and attenuation of choroidal capillaries in CSC patients have been widely recognized. However, there are few studies on their retinal capillary system, and little is known about the blood supply of the inner and middle retina of CSC among the elderly and young groups. Compared with the control group, CCPA, DCP, ICP and SCP were significantly reduced in the cCSC group. It proved that cCSC affects not only affected the choroidal vascular system, but also affected the retinal capillary system, and the whole retina was in a state of hypoperfusion. The CCPA reduction in the elderly group is particularly significant compared with the young group, suggesting that the blood supply of the outer retina in the elderly group is seriously insufficient, which corresponds to the more serious destruction of RPE [44]. At the same time, the hypoperfusion of choroidal capillaries is a trigger for increased VEGF secretion, and the risk of neovascularization is significantly increased in the elderly group. [46]The retinal capillary system provides a powerful supply for the inner and middle retinal membranes with active metabolism [45]. The decrease in blood perfusion of DCP, ICP and SCP will definitely lead to the disorder of metabolism in the corresponding retinal regions. Although there were no statistical difference in DCP, ICP, and SCP perfusion between the elderly group and the young group, the elderly group was lower in all measured ranges, which corresponded to the shorter ONL thickness and POS length in the elderly group. At present, little is known about the role of decreased retinal capillary perfusion in the pathogenesis of CSC. We believe that it may be caused by the compression of the retina by SRF. However, some patients with little SRF may also have serious severe middle and inner retinal perfusion deficits, which depends on further research.

There are limitations in this study: (1) The subjects included in the study are all Han Chinese, and the results may not be applicable to cCSC patients of other races; (2) It is a challenge to accurately identify the integrity of EZ when there are many SRFs, especially in the young group, which is expected to be solved with the further increases of OCT scanning depth; (3) This study is a cross-sectional study based on clinical data. The hypothesis proposed in this paper depends on the further confirmation from large, multicenter, and prospective studies; (4) In this study, the age cut-off value was set at 50 years old, which was determined according to the age of previous CSC and the reference age of AMD. Due to the limited number of cases, we did not further study the changes of clinical characteristics of cCSC with age in a smaller age scale, which will be the direction of our further studies.

Conclusions

In conclusion, we have described in detail the unique clinical features of elderly cCSC from the aspects of retina, choroid anatomy, and blood perfusion, and we realize that elderly cCSC patients may have different disease outcomes than young cCSC patients. Elderly cCSC patients have less gender tendency, poorer vision, more serious choroidal and retinal structural damage and ischemia, and have a higher risk of choroidal neovascularization.