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Temporal retinal thinning might be an early diagnostic indicator in male pediatric X-linked Alport syndrome

2022-07-30 10:03:32RuiLinZhuLiangZhaoXiaoPengGuYaDiZhangFangWangYanQinZhangLiuYang
International Journal of Ophthalmology 2022年7期
關(guān)鍵詞:程序防控污染

INTRODUCTION

株高與穗位高(0.45**)、株高與穗長(0.32**)、株高與穗行數(shù)(0.34**)、穗位高與空桿率(0.38**)、穗長與禿尖長(0.35**) 呈極顯著正相關(guān),活動積溫與穗長(0.21*)、株高與出籽率(0.19*)、空桿率與禿尖長(0.21*) 呈顯著正相關(guān),空桿率與出籽率(-0.32**)、百粒重與禿尖長(-0.25**)、百粒重與穗行數(shù)(-0.43**) 呈極顯著負(fù)相關(guān),百粒重與空桿率(-0.22*)、禿尖長與出籽率(-0.19*)呈顯著負(fù)相關(guān)。其余各項(xiàng)相關(guān)性均未達(dá)到0.05顯著水平。

In male patients, the TTI of the total retina (

<0.0001), inner retina layers (

<0.0001), GCL (

<0.0001), IPL (

<0.0001),INL (

<0.0001), and ONL (

=0.0012) were significantly higher in the XLAS group. Twenty-seven male patients(77.14%) had severe pathological temporal retinal thinning.All the 27 patients had severe pathological temporal retinal thinning in inner retina layer, while 24 of the male patients(68.57%) had severe temporal thinning in the INL layer. The CRT of the XLAS group (233.40±31.11 μm) was significantly thinner than that of the control group (258.90±17.11 μm;

<0.0001). Figure 3 is a representative SD-OCT result of an XLAS patient.

SUBJECTS AND METHODS

Ethical Approval The study follows the tenets of the Declaration of Helsinki. The study was approved by the Institutional Review Board of Peking University First Hospital,Beijing, China (ID: 2017-1409). All patients’ parents gave informed consent for data collection and analysis.

Participants We retrospectively reviewed the SD-OCT data and medical records of XLAS patients aged under 18y who received ophthalmic examination from January 2017 to September 2019 at Peking University First Hospital. All patients received genetic testing with Sanger sequencing or targeted whole exome sequencing. All the patients were confirmed to have a pathogenic variant in the

gene,and the diagnosis of XLAS was made at the Department of Pediatrics of Peking University First Hospital. Data evaluated included patient demographics, ocular history, slit-lamp and dilated fundus examination records. SD-OCT studies were reviewed. We recruited healthy children as a control group who received SD-OCT and ocular examination. The refractive error of these participants was between -5.75 DS to +2.75 DS.No anterior segment or fundus changes were identified in the control group children. The systemic medical history was unremarkable in the control group.

Spectral Domain Optical Coherence Tomography SD-OCT(Spectralis; Heidelberg Engineering, Heidelberg, Germany)was performed in a high-resolution mode on all patients to assess macular thickness changes. The macular cube volumetric scans were obtained centered at the fovea, including 49 B-scans and 15 automated real-time repetitions. Retinal layer segmentation was executed automatically using Spectralis OCT built-in software (Heidelberg Eye Version 1.10.2.0).

進(jìn)入21世紀(jì)以來,西藏印刷業(yè)不斷進(jìn)步,伴隨著市場經(jīng)濟(jì)的發(fā)展,印刷業(yè)從官方主辦逐步發(fā)展到市場主導(dǎo),印刷,已走進(jìn)西藏的千家萬戶。

The auto segmentation software determined 11 different retinal boundaries (Figure 1): the inner limiting membrane (ILM), the boundaries between the retinal nerve fiber layer (RNFL) and the ganglion cell layer (GCL), between the GCL and the inner plexiform layer (IPL), between the IPL and the inner nuclear layer (INL), between the INL and the outer plexiform layer(OPL), between the OPL and the outer nuclear layer (ONL),the external limiting membrane (ELM), two photoreceptor layers (PR1/2), the retinal pigment epithelium (RPE), and Bruch’s membrane (BM). Thickness of the following layers was automatically calculated: RNFL, GCL, IPL, INL, OPL,ONL, RPE, total retinal thickness (RT, comprising the ILM and BM), inner retinal layers (IRLs, comprising the ILM and the ELM), and outer retinal layers (ORLs, comprising the ELM and the BM).

All the images were reviewed by an ophthalmologist (Zhao L),who was masked to clinical information. Poor-quality images with a signal strength less than 20 dB, poor centration, or incorrect segmentation images were discarded.

當(dāng)漿液擴(kuò)散方位角90°

Temporal Thinning Index calculation According to Ahmed’s formula

, the TTI was calculated with the following formula:

N1 and N2 were the average thicknesses (μm) of the inner and outer nasal segments, respectively, and T1 and T2 were the average thicknesses (μm) of the inner and outer temporal segments, respectively (Figure 2). According to Ahmed’s report

, the TTI was subdivided into 3 categories based on the TTI mean value and SD value of the normal children in the control group. Normal physiological thinning was defined as a TTI<1 SD of the normal mean value, moderate pathological thinning was defined as a TTI 1-2 SDs above the normal mean value, and severe pathological thinning was defined as a TTI>2 SDs above the normal mean value.

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As mentioned in Chen

’s study

, there was no difference in the TTI between the right eye and left eye, so the data of the right eyes were collected in our study. The TTI of the following layers was evaluated: RNFL, GCL, IPL, INL, OPL,ONL, RPE, RT, IRLs, and ORLs.

The acoustic impedance of the perforated plate is related to the acoustic resistance and mass reactance of the orifice on the assumption that the interaction between the orifices,if they are sparsely distributed,can be neglected.

Ocular abnormalities were found as below. Dot-and-fleck retinopathy was found in 8 patients (18.60%), and all of them were male. One male patient had pseudophakia due to lenticonus (2.33%). No corneal abnormality was found in our study. Visual acuity was recorded for the patients over 8 years old, and the best corrected visual acuity for all of them was 1.0. The total retinal thickness was shown in Table 2.Compared with the control group, the temporal inner sector retinal thickness (

<0.0001), the temporal outer sector retinal thickness (

<0.0001), and the nasal outer sector retinal thickness (

=0.0211) were significantly thinner in the XLAS male patients. There was no significant difference in retinal thickness between female XLAS patients and the control group. The TTI result was shown in Table 3. The TTI of the total retina (

<0.0001) was significantly higher in the XLAS group than in the control group. According to the criteria mentioned by Ahmed

, based on the TTI mean value and SD value of the normal children in the control group, there was temporal retinal thinning in 33 patients (76.74%), while 28 patients (65.11%) had severe pathological temporal retinal thinning and 5 patients (11.63%) had moderate thinning.

RESULTS

In this retrospective study, 43 patients diagnosed with XLAS were included. Thirty-five (81.40%) of the patients were male.The mean age of the patients was 10.07±2.95 (range 4-15)y when they received the SD-OCT examination. Sixty ametropia patients were included as control subjects. The mean age of thecontrol group was 9.28±2.65 (range 5-16)y. Demographic data of the patients are shown in Table 1. There were no significant differences in age or sex between the two groups.

Statistical Analysis GraphPad Prism 9 (GraphPad Software,San Diego, USA) was used for statistical analyses. Baseline descriptive characteristics (age, sex) were compared between the healthy and XLAS groups using an unpaired Student’s

-test for quantitative variables and Fisher’s exact test for categorical variables. The CRT and TTI of different layers were compared between the groups, and a

value <0.05 was considered statistically significant. The relationship between TTI and the age of XLAS patients was determined using Spearman’s

correlation coefficient.

根據(jù)常州市“十二五”河道長效管理評估[5],“十二五”期間,60條城市內(nèi)河平均水質(zhì)綜合污染指數(shù)有所下降(RS=-0.800),污染等級由嚴(yán)重污染改善至重污染,水質(zhì)呈現(xiàn)出一定改善趨勢(見圖1)。

With automated segmentation analysis, the TTI of the inner retina layers (

<0.0001), GCL (

<0.0001), IPL (

<0.0001),INL (

<0.0001), and ONL (

<0.0001) were significantly higher in the XLAS group. There were no significant differences in the TTI in other layers. The CRT of the XLAS patients was 234.40±28.69 μm (range 168-294 μm) and 257.30±16.62 μm (range 225-293 μm) in the control group.The CRT of the XLAS group was significantly thinner than that of the control group (

<0.0001).

Ocular abnormalities were generally more prominent in male XLAS patients. In our patient group, severe temporal retinal thinning was 27 (77.14%) in male patients

1 (12.50%) in female patients, and the retinal thickness measured by SDOCT was significantly different in the male group (Table 2).Thus, we further analyzed the TTI in different sexes. The results were shown in Tables 4 and 5.

Ocular abnormalities are common in AS patients, including corneal opacities, anterior lenticonus, and dot-and-fleck retinopathy

. In recent years, researchers from different groups have reported that temporal retinal thinning is a frequently detected ophthalmic feature in AS

. The occurrence of temporal retinal thinning is more common than other ocular abnormalities and is independent of other ocular features in AS patients. Ahmed

generated a temporal thinning index (TTI) to analyze temporal retinal thinning in X-linked Alport syndrome (XLAS) patients. Their reported data revealed that in XLAS patients, 70% of the patients had severe thinning, and 11% of them had moderate thinning

.Most studies measured total retinal thickness to calculate the extent of retinal thinning, and which retinal layer changed most was not addressed. Therefore, the characteristics of retinal thinning need to be elucidated. Previous studies on temporal retinal thinning in AS have been conducted almost all in adult cohorts, and little is known about pediatric AS patients. Recently, researchers have demonstrated that retinal temporal thinning is diagnostic for XLAS in men

. Since the frequency and severity of typical ocular anomalies increase with age

, temporal retinal thinning is more sensitive than typical ocular changes. Thus, in this study, we analyzed temporal retinal thinning with spectral domain optical coherence tomography (SD-OCT) and measured the retinal thickness of different retinal layers to investigate temporal retinal thinning changes in XLAS patients. We investigated temporal thinning in pediatric patients to study this feature at an early stage of the disease.

Temporal retinal thinning is more common than other AS ocular changes,

, anterior lenticonus, the lozenge sign, or dot-and-fleck retinopathy. Among the XLAS patients included in Ahmed

’s

study, 81% of the patients had moderate to severe thinning, while less than 20% eyes had other ocular findings

. Savige

reported that 89% male XLAS patients and 75% female XLAS patients had temporal retinal thinning. In our study, 33 (76.74%) patients had moderate to severe temporal retinal thinning, while dot-and-fleck retinopathy and lenticonus were found in only 18.60% and 2.33% patients,respectively. Since temporal retinal thinning is a sensitive and specific feature of AS, Chen

and Zhao

both have identified its diagnostic value in screening AS.

DISCUSSION

Retinal temporal thinning detected with SD-OCT is demonstrated as a common ocular change in AS. In 2004, Usui

reported an AS patient with symmetrical reduced thickness of the temporal macular area in both eyes, while the visual function of the patient was normal. During the following years,some other researchers reported AS patients with focal zones of inner retinal thinning in the temporal quadrant

. In 2013,Ahmed

suggested using the TTI parameter to assess the degree of retinal temporal thinning in AS patients. The TTI parameter was then adopted by other study groups and became an important index for evaluating temporal retinal thinning in AS patients. We compared the retinal thickness in nasal and temporal sectors between XLAS patients and the control group. Since the range of variation of the retinal thickness waslarge in different papers

, the TTI was useful to address the relative thinning of the temporal quadrant. Therefore, we use the TTI as our main result. It also made the results of our study comparable to previous reports by other investigators

.

Alport syndrome (AS) is a hereditary glomerular disease characterized by hematuria and progressive renal failure. The syndrome is usually associated with sensorineural hearing loss and distinct ocular abnormalities

, and it is estimated to affect 1 in 5000-10 000 individuals

. AS is caused by mutations in the

,

, and

genes, which encode the α3, α4, and α5 chains of collagen type IV

. Approximately 85% of affected patients show an X-linked dominant inheritance form caused by mutations in the

gene

.

In female patients, the TTI of the total retina (

=0.0248)was significantly higher in the XLAS group, while the TTI of the inner retina layers (

=0.0669) and outer retina layers (

=0.1070) were not significantly different between the two groups. The CRT of the female XLAS patients(238.10±17.33 μm) was significantly thinner than that of the control group (254.10±15.54 μm;

=0.0285). Age was not correlated with retinal temporal thinning in either male patients (

=-0.1356,

=0.4372) or female patients (

=0.1537,

=0.7163).

The foveal center was automatically identified by the SD-OCT software, and it was used as the center of the Early Treatment of Diabetic Retinopathy Study (ETDRS) grid. The ETDRS grid was used to analyze the average thickness of the different layers. As described by Ahmed

, the standard 6-mm macular OCT grid as defined by the ETDRS circle was labeled with 1-, 3-, and 6-mm-diameter circles centered at the fovea.The average of all measurements within the inner 1-mm circle was defined as central retinal thickness (CRT). The average retinal thickness in each of the nine macular sectors in the 6-mm diameter circle of each layer was evaluated automatically.

However, the pathogenesis of temporal retinal thinning is not fully understood. Previous studies suggested that thinning mainly affects the ILM and RNFL

. Some researchers assumed that the temporal thinning phenomenon in AS may be related to the postnatal development of the macula, tractional vitreoretinal forces, or aberrant Müller cell adhesion

. In our study, we used SD-OCT segmentation analysis to investigate the exact layer that changes most in AS. We included only XLAS pediatric patients to eliminate interference factors and observe the changes in the early stage of the disease.

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