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Article

Therapeutic Effect of Intense Pulsed Light in Patients with Sjögren’s Syndrome Related Dry Eye

1
Eye Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310009, China
2
Second Clinical Medical School, Zhejiang Chinese Medical University, Hangzhou 310053, China
3
Zhejiang Institute of Medical Device Supervision and Testing, Hangzhou 310018, China
*
Authors to whom correspondence should be addressed.
J. Clin. Med. 2022, 11(5), 1377; https://doi.org/10.3390/jcm11051377
Submission received: 13 January 2022 / Revised: 16 February 2022 / Accepted: 24 February 2022 / Published: 2 March 2022
(This article belongs to the Special Issue Advances in the Diagnosis and Treatment of Ocular Surface Diseases)

Abstract

:
This prospective randomized study evaluated the efficacy and safety of intense pulsed light (IPL) and meibomian gland expression (MGX) as polytherapy for Sjögren’s Syndrome-related dry eye (SS-DE). The study enrolled 55 participants with SS-DE, 27 for the treatment group and 28 for the control group. The treatment group underwent three IPL-MGX treatments, three weeks apart. A randomly-selected eye from each patient was assessed at baseline and on weeks 9, 12, and 15 for Snellen best-corrected visual acuity (BCVA), intraocular pressure, Ocular Surface Disease Index (OSDI) score, conjunctival congestion, tear meniscus height, non-invasive tear breakup time (NBUT), Schirmer’s I test (SIT), corneal fluorescein staining (CFS), meibomian gland (MG) dropout, eyelid margin abnormality, MGX and meibum quality. OSDI, NBUT, CFS, MGX, and meibum quality were significantly improved in both groups, particularly in the treatment group. The eyelid margin abnormality improved significantly in the treatment but not in the control group on weeks 12 and 15. Snellen BCVA, conjunctival congestion, and SIT improved significantly in the treatment group, but the two groups were statistically similar. Our results indicated that three IPL-MGX sessions could significantly improve the subjective and objective characteristics of SS-DE, representing a promising treatment strategy.

1. Introduction

Sjögren’s syndrome (SS) is an autoimmune disease characterized by the lymphocytic infiltration of the moisture-producing glands, including the sebaceous, sweat, salivary, and lacrimal glands, resulting in its two most common symptoms: dry eyes (DE) and a dry mouth [1,2]. The disease might have other concomitant systemic displays [3]. The SS-associated DE (SS-ED) severely affects the patients’ quality of life and activity range. While SS-DE might have a range of ocular presentations, the most common is keratoconjunctivitis sicca (KCS). Patients with SS-DE show significantly more serious signs and symptoms, including poorer and more blurred vision than those with non-SS DE [4].
Traditionally, DE was conveniently divided into the aqueous-deficient and evaporative subgroups. These two DE subgroups differ in the pathophysiological and background aspect of their DE. Patients with SS are classified exclusively into the aqueous-deficient DE subgroup because their damaged lacrimal glands secrete less of the tears’ aqueous portion, but they might also present meibomian gland (MG) dysfunction (MGD) [5]. Therefore, patients with SS should be treated for both DE subtypes.
The treatment for SS-DE depends on the severity of the symptoms. Artificial tears or lubricants are sufficient at the early stage of the disease [6]. Patients with a progressive or more severe disease might need topical corticosteroids [7] or cyclosporine [8]. Other treatment options include dietary supplements of omega-3 essential fatty acids [9] and the use of punctal plugs [10]. SS, particularly progressive SS, remains difficult to manage despite the various available treatment options. Some patients with SS might present with DE resistant to the treatment options mentioned above. The most severe cases, particularly those unresponsive to topical corticosteroids or cyclosporine, could be considered for applying topical autologous serum or partial tarsorrhaphy to reduce environmental exposure and evaporation [11].
Intense pulsed light (IPL) has been widely used to treat evaporative DE, mostly secondary to MGD [12,13] or ocular demodicosis [14]. As far as we know, only one retrospective study has reported using IPL to treat seven patients with SS-DE [15]. However, that previous study was not randomized or performed in a masked manner. Therefore, this is the first study to evaluate the therapeutic effects and safety of IPL and MG expression (MGX) as polytherapy for SS-DE.

2. Materials and Methods

2.1. Subjects

This study followed the tenets of the Declaration of Helsinki. The Ethics Committee of The Second Affiliated Hospital of Zhejiang University School of Medicine approved the study (No. 2019-270). The study was registered as a clinical trial on 9 August 2020 (ChiCTR2000035344). All patients provided written informed consent before enrollment in this research.
Rheumatologists diagnosed SS in all participants following the Sjogren’s International Collaborative Clinical Alliance (SICCA) classification criteria from 2012 [16]. These criteria comprise (1) serum positive for anti-SSA/Ro or anti-SSB/La, or positive rheumatoid factor and antinuclear antibody titer ≥ 1:320; (2) histological assessment showing labial salivary gland infection with lymphocytic focus score ≥ 1 per 4 mm2; (3) a score of ≥3 for KCS during corneal staining. Refractory SS-DE was determined when a patient failed to respond to at least three standard treatment approaches through management for one year or more. These treatments included lubricant eye drops, topical ointment, warm compress and massage of the eyelid, topical anti-inflammatory therapy, moisture chamber spectacles, and for those not currently using-contact lenses, punctal plugs and systemic immunosuppression.

2.2. Experimental Design

We randomly assigned patients with SS-DE aged 18-70 years to the IPL-MGX treatment or control group. Patients in the IPL-MGX group underwent three IPL-MGX treatments three weeks apart and three follow-up assessments 9, 12, and 15 weeks from the start of treatment. All participants were prescribed sodium hyaluronate eye drops four times daily during the study and follow-up. The patients were allowed to continue with home care such as warm compresses and lid hygiene.
A day before the first treatment and at each follow-up assessment, the treatment efficiency was evaluated using Snellen best correct visual acuity (BCVA), intraocular pressure (IOP), Ocular Surface Disease Index (OSDI) score, conjunctival congestion, non-invasive breakup time of tear film (NBUT), Schirmer’s I test (SIT), tear meniscus height (TMH), corneal fluorescence staining (CFS), MG dropout, eyelid margin abnormalities, MGX, and meibum quality.
CFS was considered the primary outcome measure, while the secondary outcome measures included OSDI score, TBUT, MG dropout, eyelid margin abnormalities, MGX, meibum quality, SIT, TMH, and conjunctival congestion. The treatment safety was assessed by Snellen BCVA, IOP and slit lamp examination. In this investigation, one eye from each patient was randomly chosen and evaluated.

2.3. IPL-MGX Treatment

The M22 IPL system (Lumenis, Tel Aviv, Israel), set for the AOPT mode, was used in this research. The energy parameters were estimated based on Fitzpatrick skin type and the patient’s tolerance and comfort (density, 15–17 J/cm2). Each patient received two perpendicular IPL treatments, once from each side. The treatment from the right included the cheeks and nose, while the one from the left extended the interior margin of the protective eye shields. An Aritia Meibomian Gland Compressor (Katena Product Inc., Denville, NJ, USA) was used to perform the MGX on the upper and lower eyelids immediately after the IPL therapy. The patients in this group were given 0.4% oxybuprocaine hydrochloride eye drops (Santen Pharmaceutical Co., Ltd., Osaka, Japan) for pain relief through the procedure.
An additional inclusion criterion was Fitzpatrick skin types of 1–4 [17]. Patients were excluded if they had implants in the treatment area; cosmetic eyelid surgery in the last five years; glaucoma; graft-versus-host disease, autoimmune connective tissue diseases other than rheumatoid arthritis or lupus; acute solar dermatitis; allergic disease; had eye surgery less than three months earlier; any physical or mental condition interfering with successful participation in the study; recent LipiFlow or MGX treatment.

2.4. Clinical Assessment

2.4.1. Ocular Surface Disease Index (OSDI)

The clinical parameters evaluated were similar to our previous study [14]. The 12-item OSDI questionnaire assessed the ocular surface-related symptoms and their severity and frequency. The sum of all 12 OSDI items would result in a score of 0–100 points.

2.4.2. Schirmer’s I Test (SIT)

The SIT was performed without anesthesia. A sterile dry strip of filter paper (Jingming New Technological Development Co., Ltd., Tianjin, China) was placed inside the inferior fornix for 5 min. The length of the moistened area on the strip determined the lacrimal gland functionality.

2.4.3. Tear Meniscus Height (TMH) and Conjunctival Hyperemia

The lower TMH and conjunctival hyperemia were assessed automatically by the OCULUS Keratograph 5M (OCULUS Optikgeräte GmbH, Wetzlar, Germany).

2.4.4. Tear Film Stability

NBUT was measured using the OCULUS Keratograph 5M (OCULUS Optikgeräte GmbH, Wetzlar, Germany). We asked the patients to blink several times before leaving their eyes open without blinking. We measured the time in seconds from the last complete blink to the first disturbance or irregularity of the concentric rings reflected on the cornea surface. The average NBUT of three tests was recorded.

2.4.5. Corneal Fluorescein Staining (CFS)

CFS was performed with a moist fluorescein strip (Jinming New Technological Development Co., Ltd., Tianjin, China). The cornea was divided into five sections (superior, temporal, nasal, inferior, and central), and a staining severity was assigned to each, ranging from 0 (no staining) to 3 (severe).

2.4.6. Meibomian Gland (MG) Morphology

Meibography was rated by the OCULUS Keratograph 5M (OCULUS Optikgeräte GmbH, Wetzlar, Germany) on a scale of 0–3: 0, no gland loss; 1, <1/3 lost area; 2, area of loss between 1/3 and 2/3; and 3, >2/3 lost area.

2.4.7. Eyelid Margin Abnormalities

The eyelid margins were assessed for abnormalities on a 0–4 scale following these four criteria: irregular eyelid margins, vascular engorgement, clogged MG ducts, and displaced mucocutaneous junction.

2.4.8. Meibomian Gland Expression (MGX)

The MG Evaluator assessed the MGX on the on lower tarsal plate. The eyelid was divided into three sections (nasal, central, and temporal). Each section contained five glands. We counted the glands expressing meibum in each section and rated the expression as follows: 0, normal; 1, 3–4 glands expressed; 2, 1–2 glands expressed; 3, no gland expression. The total MGX score could be in the range of 0–9.

2.4.9. Meibum Quality

Each of eight MGs in the center of the lower eyelid was rated on a scale of 0–3: 0, no secretion; 1, inspissated, toothpaste-like fluid; 2, viscous, opaque, or yellow fluid; 3, clear fluid (total score range, 0–24).

2.4.10. Safety Assessments

Treatment safety was evaluated by the Snellen BCVA, IOP, and slit-lamp examination performed at the start of the study and during each follow-up session.

2.5. Statistical Analysis

A statistical analysis was performed using IBM SPSS Statistics for Windows, Version 25.0 (IBM Corp., Armonk, NY, USA). We performed a sample size calculation following the method used in previous studies [18,19,20]. We hypothesized that the CFS results would differ by 25% between the IPL-MGX and control groups. Based on this assumption, a power of 90%, and a two-sided significance level of 0.05, our study needed 24 patients in each group. Only data of patients completing the entire study were analyzed. Continuous variables are presented as means ± standard deviations (SDs). The Shapiro-Wilk test assessed these variables for normal distribution. The paired-samples t-test or paired Mann-Whitney U test compared continuous variables between baseline and the follow-up assessments. The control and IPL-MGX groups were compared by the independent-sample t-test or Mann-Whitney U test at baseline and after the treatment period. Statistical significance was set at p < 0.05.

3. Results

This prospective randomized controlled trial enrolled 55 patients with SS upon diagnosis with bilateral DE. One patient in the IPL-MGX group could not adhere to the follow-up schedule due to the COVID-19 quarantine policy and left the study. Four of the control group patients left the study because they saw no relief in their DE symptoms. All analyses was based on the remaining participants. Figure 1 presents an outline of the study and its stages (recruitment, withdrawal, treatment sessions, and follow-up assessments).
Fifty patients, one male (2%) and forty-nine females (98%), completed the study. The IPL-MGX group was comprised of 26 patients, a male and 25 females, aged 53.46 ± 10.71 (range, 32–78) years. The control group was comprised of 24 patients, all female, aged 51.71 ± 13.32 (range, 30–67) years. The groups were similar in age, DE, and SS medical history. Refractory SS-DE occurred in 23 patients (88.46%) in the treatment group and 21 (87.5%) in the control group. As shown in Table 1, the groups were similar in their patient characteristics.
The groups were compared for the parameters assessed during each visit (Table 2). The time courses of Snellen BCVA, ODSI, NBUT, CFS, eyelid margin abnormality, MGX and meibum quality are presented in Figure 2, Figure 3 and Figure 4. The groups were similar in all parameters at baseline. The Snellen BCVA score at three follow-up assessments was lower than at baseline in the IPL-MGX group (all p ≤ 0.001), while the control group remained unchanged (all p > 0.05; Figure 2A). The OSDI scores were lower than at baseline in all three follow-up assessments in both groups (all p < 0.05). All three follow-up scores in the IPL-MGX group were considerably lower than in the control group (all p < 0.001; Figure 2B). Compared to baseline, the two groups showed higher NBUT (Figure 3A) and lower CFS (Figure 3B) at all follow-up assessments (all p < 0.05). The improvement in NBUT and CFS in the treatment group was greater than in the control group when assessed on weeks 12 and 15 (all p < 0.05). Compared to baseline, a significant decrease in eyelid margin abnormalities (Figure 4A) and a substantial increase in MGX (Figure 4B) and meibum quality (Figure 4C) were apparent at all three follow-up sessions in the IPL-MGX group (all p > 0.05). Significant improvements in the MGX and meibum quality were also noted at weeks 12 and 15 in the control group (all p > 0.05). The eyelid margin abnormalities remained unchanged throughout the study in the control group (all p > 0.05). The eyelid margin abnormalities, MGX and meibum quality in the IPL-MGX group differed significantly from those in the control groups (all p > 0.05), except for MGX at the week 15 assessment (p = 0.094).
We found similar Snellen BCVA, conjunctival congestion, TMH, and SIT at weeks 9, 12, and 15 in the two groups. MG dropouts did not change over the four visits in either group (all p > 0.05).
The KCS-specific symptoms have improved following the IPL-MGX treatment. Figure 5 and Figure 6 show two representative cases of patients with SS-DE in the IPL-MGX group who exhibited significant improvement in their ocular surface conditions between baseline and the final follow-up visit. Both patients had notable ocular surface inflammation, poor vision, and could barely open their eyes before treatment (Figure 5A–D and Figure 6A–D). Case 3 (Figure 5) was a 60-year-old female with SS for 14 years and DE for 13 years. The patient was previously treated with topical and oral corticosteroids, topical cyclosporine, and autologous serum, but none achieved disease progression control. The patient showed severe symptoms including strong foreign body sensation, burning, stinging, photophobia, blurred vision, and ocular pain. Case 11 (Figure 6) was a 36-year-old female with SS for 7 years and DE for 5 years. The patient had similar ocular irritation symptoms as in case 3. Previously treatments with topical corticosteroids, cyclosporine, artificial tear eye drops, warm compresses combined with MGX, and eyelid hygiene had failed. Reduced filamentary keratitis, corneal epithelial healing, and improved vision were noted at last follow-up in both cases (case 3: Figure 5E–H, case 11: Figure 6E–H).

4. Discussion

SS is a chronic, currently incurable, and potentially deadly disease. Cell-mediated immunity plays an important role in the pathogenesis of SS-DE [3]. Although it is traditionally classified as aqueous tear-deficient DE, mounting evidence suggests that ocular surface inflammation is not limited to the lacrimal glands [21]. An inflammation cascade is initiated on the ocular surface by lymphocytic infiltration and the increase in cellular inflammatory mediators. This cascade might cause an imbalance among the components of the complex ocular system that include the eyelid, tears, mucous, and epithelial surfaces. We believed the inflammation of the ocular surface and exocrine glands, and the diminished neural innervation, could further impair the accessory lacrimal glands, corneal epithelial cells, goblet cells, and MGs. These damages result in deficiency of all the tear film constituents, leading to the observed presentation that is often more severe than in non-SS DE. Unlike those with non-SS DE, patients with SS-DE were reported to have poorer vision and quality of life [5].
Controlling inflammation may play an important role in treating SS-DE. However, the management of SS-DE in clinical practice could be challenging for ophthalmologists. Topical corticosteroids, cyclosporine, and even autologous serum often achieve only temporary and partial improvement, possibly because this complex pathology is only partially understood, resulting in symptom-oriented treatment rather than the targeting of the cause. Most patients in our study (IPL-MGX group: n = 23, 88.5%; control group: n = 21, 87.5%) had refractory SS-DE before recruitment. Patients with moderate to severe ocular surface conditions, such as persistent filamentary keratitis and corneal epithelium defect, might not respond well to conventional anti-inflammatory medication and may require additional measures.
As far as we are aware, only one previous IPL study was performed, and that study included only a few patents with SS-DE (seven in the IPL-MGX treatment group and six in the control group) [15]. That study had several limitations. First, both eyes of each participant were included, which, statistically, is not considered best practice. Second, these thirteen patients were recruited from three centers with no detailed and consistent diagnostic criteria such as serological testing or labial salivary gland biopsy. Third, all patients were allowed to continue their various ocular medications during the study. Moreover, there might be a high risk of bias, as it was not randomized or performed in a masked manner. All these important confounding factors reduce the confidence in the reported results.
Our study was the first prospective randomized controlled trial to demonstrate the beneficial effects of the IPL-MGX treatment in patients with SS-DE. The patients in our study were randomly assigned to the IPL-MGX or the control group. The treatment group patients received three IPL-MGX treatments at three-week intervals. All characteristics were assessed at baseline and on weeks 9, 12, and 15 after the first treatment. Some of the measured parameters have improved through follow-up in both study groups, but the IPL-MGX groups showed greater improvement than the control group in the OSDI score, NBUT (weeks 12 and 15), CFS (weeks 12 and 15), eyelid margin abnormalities, MGX (weeks 9 and 12), and meibum quality. These findings were consistent with our earlier studies showing the effectiveness of IPL as a treatment for MGD and ocular demodicosis [14,22].
The Snellen BCVA score was included for safety assessment when we designed this experiment. Unexpectedly, the vision of participants treated with IPL-MGX showed a remarkable improvement that persisted through all three follow-up assessments (all p < 0.001), unlike the patients with non-SS DE in our previous IPL experiment [14]. Although the differences between the treatment and control groups did not reach the significance level, we were satisfied with the significant improvement in visual acuity in some patients, including those in which topical cyclosporine or autologous serum treatment had failed. The lower CFS and improved vision might suggest that the IPL treatment enhanced the integrity of the ocular surface. The decreased inflammation and improved ocular surface could initiate a cascade that includes improved corneal sensory nerve ending activation, enhanced neural signals to the lacrimal gland, and improved tear secretion. These could result in the improvement seen in SIT and TMH in this study.
Although the mechanism of the IPL treatment remains unclear, we believe that the main reason for the improved vision in the patients with SS is that IPL reduced the ocular surface inflammation considerably, lowering apoptosis of the corneal epithelial and conjunctival goblet cells and filamentary keratitis, and improving the MGD symptoms and signs. Similar patterns were observed for conjunctival congestion and SIT, with IPL-MGX leading to a significant improvement over baseline not seen in the control group. However, the differences in these parameters between the two groups were statistically insignificant in this study (all p > 0.05). Our findings suggest that IPL could improve vision and reduce ocular surface inflammation in patients with SS-DE.
This study had several limitations. We used an IPL protocol for MGD-related DE (three IPL-MGX treatment sessions at three-week intervals). However, it seems that unlike patients with non-SS DE, those with SS and severe ocular surface damage might need more than three IPL treatment sessions or shorter inter-treatment intervals. Moreover, the most severe cases may require combination therapy that includes topical corticosteroids or cyclosporine eyedrops. Therefore, a further long-term study with a combination therapy study is necessary to better understand the effectiveness and mechanism of the IPL-MGX treatment.

5. Conclusions

In conclusion, our study showed IPL-MGX to be a promising treatment regimen for patients with SS-DE, especially those refractory to the standard therapies. Further studies might promote other therapeutic possibilities; however, our findings indicate that IPL-MGX significantly improves the objective and subjective disease characteristics in patients with SS-DE.

Author Contributions

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Natural Science Foundation of Zhejiang Province [LY20H120009]; National Natural Science Foundation of China [31751003, 82171013]; Health Commission of Zhejiang Province [2022KY168], Beijing Bethune Charitable Foundation BJ-GY2021013J; Major Science and Technology Projects of Zhejiang Province [2022C03173].

Institutional Review Board Statement

This study was conducted according to guidelines of the Declaration of Helsinki, and approved by the Ethics Committee of The Second Affiliated Hospital of Zhejiang University School of Medicine (protocol code 2019-270, date 29 December 2019). The study was registered as a clinical trial on 9 August 2020 (ChiCTR2000035344). All patients provided written informed consent before enrollment in this research.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Individual deidentified participant data (including data dictionaries) will be shared. All the individual participant data collected during the trial, after deidentification, Study Protocol, Statistical Study Protocol, Statistical Analysis Plan, Analytic Code, and Study Protocol will be available beginning 6 months and ending 1 year following article publication to anyone who wishes to access the data to achieve aims in the approved proposal. Proposals should be directed to [email protected]. Data requestors will need to sign a data access agreement.

Conflicts of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. Moutsopoulos, H.M. Sjogren’s syndrome: Autoimmune epithelitis. Clin. Immunol. Immunopathol. 1994, 72, 162–165. [Google Scholar] [CrossRef] [PubMed]
  2. Skopouli, F.N.; Fox, P.C.; Galanopoulou, V.; Atkinson, J.C.; Jaffe, E.S.; Moutsopoulos, H.M. T cell subpopulations in the labial minor salivary gland histopathologic lesion of Sjogren’s syndrome. J. Rheumatol. 1991, 18, 210–214. [Google Scholar] [PubMed]
  3. Uchino, M.; Schaumberg, D.A. Dry Eye Disease: Impact on Quality of Life and Vision. Curr. Ophthalmol. Rep. 2013, 1, 51–57. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Bjordal, O.; Norheim, K.B.; Rodahl, E.; Jonsson, R.; Omdal, R. Primary Sjogren’s syndrome and the eye. Surv. Ophthalmol. 2020, 65, 119–132. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Wang, Y.; Qin, Q.; Liu, B.; Fu, Y.; Lin, L.; Huang, X.; Jin, X. Clinical Analysis: Aqueous-Deficient and Meibomian Gland Dysfunction in Patients With Primary Sjogren’s Syndrome. Front. Med. 2019, 6, 291. [Google Scholar] [CrossRef]
  6. Foulks, G.N.; Forstot, S.L.; Donshik, P.C.; Forstot, J.Z.; Goldstein, M.H.; Lemp, M.A.; Nelson, J.D.; Nichols, K.K.; Pflugfelder, S.C.; Tanzer, J.M.; et al. Clinical guidelines for management of dry eye associated with Sjogren disease. Ocul. Surf. 2015, 13, 118–132. [Google Scholar] [CrossRef]
  7. Hong, S.; Kim, T.; Chung, S.H.; Kim, E.K.; Seo, K.Y. Recurrence after topical nonpreserved methylprednisolone therapy for keratoconjunctivitis sicca in Sjogren’s syndrome. J. Ocul. Pharmacol. Ther. 2007, 23, 78–82. [Google Scholar] [CrossRef]
  8. Sall, K.; Stevenson, O.D.; Mundorf, T.K.; Reis, B.L. Two multicenter, randomized studies of the efficacy and safety of cyclosporine ophthalmic emulsion in moderate to severe dry eye disease. CsA Phase 3 Study Group. Ophthalmology 2000, 107, 631–639. [Google Scholar] [CrossRef]
  9. Rosenberg, E.S.; Asbell, P.A. Essential fatty acids in the treatment of dry eye. Ocul. Surf. 2010, 8, 18–28. [Google Scholar] [CrossRef]
  10. Qiu, W.; Liu, Z.; Ao, M.; Li, X.; Wang, W. Punctal plugs versus artificial tears for treating primary Sjogren’s syndrome with keratoconjunctivitis SICCA: A comparative observation of their effects on visual function. Rheumatol. Int. 2013, 33, 2543–2548. [Google Scholar] [CrossRef]
  11. Petznick, A.; Tong, L.; Chung, R.; Wang, J.C.; Koh, M.; Salleh, R.; Waduthantri, S. Autologous plasma eyedrops prepared in a closed system: A treatment for dry eye. Eye 2013, 27, 1102. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Craig, J.P.; Chen, Y.H.; Turnbull, P.R. Prospective trial of intense pulsed light for the treatment of meibomian gland dysfunction. Investig. Ophthalmol. Vis. Sci. 2015, 56, 1965–1970. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Dell, S.J.; Gaster, R.N.; Barbarino, S.C.; Cunningham, D.N. Prospective evaluation of intense pulsed light and meibomian gland expression efficacy on relieving signs and symptoms of dry eye disease due to meibomian gland dysfunction. Clin. Ophthalmol. 2017, 11, 817–827. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Huo, Y.; Mo, Y.; Wu, Y.; Fang, F.; Jin, X. Therapeutic effect of intense pulsed light with optimal pulse technology on meibomian gland dysfunction with and without ocular Demodex infestation. Ann. Transl. Med. 2021, 9, 238. [Google Scholar] [CrossRef] [PubMed]
  15. Arita, R.; Fukuoka, S.; Mizoguchi, T.; Morishige, N. Multicenter Study of Intense Pulsed Light for Patients with Refractory Aqueous-Deficient Dry Eye Accompanied by Mild Meibomian Gland Dysfunction. J. Clin. Med. 2020, 9, 3467. [Google Scholar] [CrossRef]
  16. Shiboski, S.C.; Shiboski, C.H.; Criswell, L.; Baer, A.; Challacombe, S.; Lanfranchi, H.; Schiodt, M.; Umehara, H.; Vivino, F.; Zhao, Y.; et al. American College of Rheumatology classification criteria for Sjogren’s syndrome: A data-driven, expert consensus approach in the Sjogren’s International Collaborative Clinical Alliance cohort. Arthritis Care Res. 2012, 64, 475–487. [Google Scholar] [CrossRef] [PubMed]
  17. Fitzpatrick, T.B. The validity and practicality of sun-reactive skin types I through VI. Arch. Dermatol. 1988, 124, 869–871. [Google Scholar] [CrossRef]
  18. Hong, H.; Choi, Y.; Hahn, S.; Park, S.K.; Park, B.J. Nomogram for sample size calculation on a straightforward basis for the kappa statistic. Ann. Epidemiol. 2014, 24, 673–680. [Google Scholar] [CrossRef]
  19. Zhang, X.; Song, N.; Gong, L. Therapeutic Effect of Intense Pulsed Light on Ocular Demodicosis. Curr. Eye Res. 2019, 44, 250–256. [Google Scholar] [CrossRef]
  20. Arita, R.; Fukuoka, S.; Morishige, N. Therapeutic efficacy of intense pulsed light in patients with refractory meibomian gland dysfunction. Ocul. Surf. 2019, 17, 104–110. [Google Scholar] [CrossRef]
  21. Wei, Y.; Asbell, P.A. The core mechanism of dry eye disease is inflammation. Eye Contact Lens 2014, 40, 248–256. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Yan, X.; Hong, J.; Jin, X.; Chen, W.; Rong, B.; Feng, Y.; Huang, X.; Li, J.; Song, W.; Lin, L.; et al. The Efficacy of Intense Pulsed Light Combined With Meibomian Gland Expression for the Treatment of Dry Eye Disease Due to Meibomian Gland Dysfunction: A Multicenter, Randomized Controlled Trial. Eye Contact Lens 2021, 47, 45–53. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The treatment protocol and follow-up schedule for the intense pulsed light (IPL)-meibomian gland expression (MGX) and control groups are presented.
Figure 1. The treatment protocol and follow-up schedule for the intense pulsed light (IPL)-meibomian gland expression (MGX) and control groups are presented.
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Figure 2. Time course of Snellen best–corrected visual acuity (BCVA) and Ocular Surface Disease Index (OSDI) score in the intense pulsed light (IPL)–meibomian gland expression (MGX) and control groups. (A) Changes of BCVA before and after treatment. (B) Changes of OSDI score before and after treatment. All follow–up assessments were compared to baseline (time 0) values (* p < 0.05, ** p < 0.001).
Figure 2. Time course of Snellen best–corrected visual acuity (BCVA) and Ocular Surface Disease Index (OSDI) score in the intense pulsed light (IPL)–meibomian gland expression (MGX) and control groups. (A) Changes of BCVA before and after treatment. (B) Changes of OSDI score before and after treatment. All follow–up assessments were compared to baseline (time 0) values (* p < 0.05, ** p < 0.001).
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Figure 3. Time course of non–invasive tear breakup time (NBUT) and corneal fluorescein staining (CFS) in the intense pulsed light (IPL)–meibomian gland expression (MGX) and control groups. (A) Changes of NBUT before and after treatment. (B) Changes of CFS before and after treatment. All follow–up assessments were compared to the baseline (time 0) values (* p < 0.05, ** p < 0.001).
Figure 3. Time course of non–invasive tear breakup time (NBUT) and corneal fluorescein staining (CFS) in the intense pulsed light (IPL)–meibomian gland expression (MGX) and control groups. (A) Changes of NBUT before and after treatment. (B) Changes of CFS before and after treatment. All follow–up assessments were compared to the baseline (time 0) values (* p < 0.05, ** p < 0.001).
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Figure 4. Time course of eyelid margin abnormalities, meibomian gland expressibility (MGX), and meibum quality in the intense pulsed light (IPL)–meibomian gland expression (MGX) and control groups. (A) Changes of lid margin abnormality before and after treatment. (B) Changes of MGX before and after treatment. (C) Changes of meibum quality before and after treatment. All follow-up assessments were compared to the baseline (time 0) values (* p < 0.05, ** p < 0.001).
Figure 4. Time course of eyelid margin abnormalities, meibomian gland expressibility (MGX), and meibum quality in the intense pulsed light (IPL)–meibomian gland expression (MGX) and control groups. (A) Changes of lid margin abnormality before and after treatment. (B) Changes of MGX before and after treatment. (C) Changes of meibum quality before and after treatment. All follow-up assessments were compared to the baseline (time 0) values (* p < 0.05, ** p < 0.001).
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Figure 5. Case 3 in the IPL-MGX group exhibited considerable improvement in the ocular surface condition from baseline to the last follow-up assessment. Images of the ocular surface and corneal fluorescein staining of both eyes at baseline (AD) and during the last follow-up visit (EH).
Figure 5. Case 3 in the IPL-MGX group exhibited considerable improvement in the ocular surface condition from baseline to the last follow-up assessment. Images of the ocular surface and corneal fluorescein staining of both eyes at baseline (AD) and during the last follow-up visit (EH).
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Figure 6. Case 11 in the IPL-MGX group exhibited considerable improvement in the ocular surface condition from baseline to last follow-up assessment. Images of the ocular surface and corneal fluorescein staining of both eyes at baseline (AD) and during the last follow-up visit (EH).
Figure 6. Case 11 in the IPL-MGX group exhibited considerable improvement in the ocular surface condition from baseline to last follow-up assessment. Images of the ocular surface and corneal fluorescein staining of both eyes at baseline (AD) and during the last follow-up visit (EH).
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Table 1. Characteristics of the study subjects in the intense pulsed light (IPL)-meibomian gland expression (MGX) and control groups.
Table 1. Characteristics of the study subjects in the intense pulsed light (IPL)-meibomian gland expression (MGX) and control groups.
CharacteristicIPL-MGX Group (n = 26)Control Group (n = 24)p-Value
Age (year), mean SD (range)53.46 ± 10.71
(32–78)
51.71 ± 13.32
(30–67)
0.861
Sex (male/female)1/250/241.000
History of DE (years), mean SD (range)6.38 ± 4.34
(1–14)
6.92 ± 5.14
(1–16)
0.792
History of SS (years), mean SD (range)8.19 ± 4.72
(1–17)
8.29 ± 5.38
(1–20)
0.961
Refractory SS-DE23 (88.46%)21 (87.5%)1.000
Previous treatmentsLubricant eyedrops or ointment26230.968
warm compress and massage23221.000
Topical anti-inflammatory19170.860
Contact lenses111.000
Moisture chamber spectacles211.000
Punctal plugs111.000
Systemic immunosuppression14110.571
SS: Sjögren’s syndrome, DE: dry eye.
Table 2. Characteristics of the intense pulsed light (IPL)-meibomian gland expression (MGX) and control groups before and after treatment.
Table 2. Characteristics of the intense pulsed light (IPL)-meibomian gland expression (MGX) and control groups before and after treatment.
CharacteristicGroupBL9 Weeks after Treatment Onset12 Weeks after Treatment Onset15 Weeks after Treatment Onset
Mean ± SDp-Value forMean ± SDp-Value vs.p-Value forMean ± SDp-Value vs.p-Value forMean ± SDp-Value vs.p-Value for
IPL-MGX vs.
Control
BLIPL-MGX vs.
Control
BLIPL-MGX vs.
Control
BLIPL-MGX vs.
Control
BCVA
(logMAR)
IPL-MGX group0.31 ± 0.290.6250.15 ± 0.170.0010.3520.15 ± 0.17<0.0010.3410.16 ± 0.18<0.0010.352
control0.31 ± 0.370.30 ± 0.360.1090.31 ± 0.370.5810.31 ± 0.381.000
OSDI
(0–100)
IPL-MGX group77.20 ± 15.180.93448.34 ± 18.70<0.001<0.00141.57 ± 17.14<0.001<0.00144.42 ± 15.44<0.001<0.001
Control76.68 ± 16.3972.07 ± 18.700.00272.53 ± 16.310.02870.74 ± 16.800.002
Conjunctival congestionIPL-MGX group1.82 ± 0.770.8311.65 ± 0.580.0740.6061.55 ± 0.560.0050.1631.53 ± 0.580.0020.227
Control1.80 ± 0.661.75 ± 0.640.0871.80 ± 0.670.8851.75 ± 0.620.091
TMH (mm)IPL-MGX group0.13 ± 0.040.4530.14 ± 0. 040.2530.8690.16 ± 0.040.0130.4530.15 ± 0.03 0.0370.837
Control0.14 ± 0.040.14 ± 0.040.4450.15 ± 0.040.0050.15 ± 0.04<0.001
SIT (mm/5min)IPL-MGX group3.42 ± 2.800.9294.27 ± 2.990.2480.3373.85 ± 1.740.2010.7984.62 ± 2.450.0240.306
Control3.62 ± 3.003.75 ± 3.340.7184.20 ± 3.370.0544.08 ± 3.270.069
NBUT (s)IPL-MGX group2.23 ± 2.590.8004.15 ± 3.580.0010.5514.82 ± 3.17<0.0010.0095.08 ± 2.433<0.0010.006
Control2.24 ± 2.482.94 ± 3.010.0012.76 ± 2.260.0192.92 ± 2.450.007
Corneal fluorescence staining (0–15)IPL-MGX group9.00 ± 5.490.8227.27 ± 5.130.0010.3994.65 ± 3.83<0.0010.0014.08 ± 3.72<0.0010.001
Control9.54 ± 4.418.67 ± 4.570.0028.75 ± 4.570.0038.54 ± 4.460.003
MG dropouts (0–3)IPL-MGX group1.58 ± 1.240.5021.46 ± 1.2170.2570.2831.46 ± 1.170.2570.2831.46 ± 1.170.2570.283
control1.79 ± 1.101.79 ± 1.101.0001.79 ± 1.101.0001.79 ± 1.11.000
Lid margin abnormality (0–4)IPL-MGX group2.73 ± 1.340.9681.96 ± 0.96<0.0010.0261.92 ± 0.93<0.0010.0121.96 ± 0.10<0.0010.019
control2.75 ± 1.332.67 ± 1.270.3172.70 ± 1.290.0832.67 ± 1.240.157
MG expressibility (0–9)IPL-MGX group6.00 ± 3.29 0.7333.88 ± 2.72<0.0010.0263.73 ± 2.22<0.0010.0404.12 ± 2.320.0020.094
control5.83 ± 3.125.71 ± 3.000.4295.21 ± 2.890.0015.25 ± 2.910.003
meibum quality (0–24)IPL-MGX group5.92 ± 7.16 0.36013.26 ± 8.40<0.0010.00315.35 ± 7.49<0.001<0.00114.92 ± 6.25<0.0010.001
control6.88 ± 7.577.21 ± 7.730.1147.54 ± 7.580.0137.63 ± 7.600.007
BCVA: best corrected visual acuity, OSDI: ocular surface disease index, TMH: tear meniscus height, NBUT: non-invasive break up time of tear film, SIT: Schirmer I test, MG: meibomian gland.
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Huo, Y.; Wan, Q.; Hou, X.; Zhang, Z.; Zhao, J.; Wu, Z.; Jin, X. Therapeutic Effect of Intense Pulsed Light in Patients with Sjögren’s Syndrome Related Dry Eye. J. Clin. Med. 2022, 11, 1377. https://doi.org/10.3390/jcm11051377

AMA Style

Huo Y, Wan Q, Hou X, Zhang Z, Zhao J, Wu Z, Jin X. Therapeutic Effect of Intense Pulsed Light in Patients with Sjögren’s Syndrome Related Dry Eye. Journal of Clinical Medicine. 2022; 11(5):1377. https://doi.org/10.3390/jcm11051377

Chicago/Turabian Style

Huo, Yanan, Qi Wan, Xinzhu Hou, Zhiyong Zhang, Jinchuan Zhao, Zhiyi Wu, and Xiuming Jin. 2022. "Therapeutic Effect of Intense Pulsed Light in Patients with Sjögren’s Syndrome Related Dry Eye" Journal of Clinical Medicine 11, no. 5: 1377. https://doi.org/10.3390/jcm11051377

APA Style

Huo, Y., Wan, Q., Hou, X., Zhang, Z., Zhao, J., Wu, Z., & Jin, X. (2022). Therapeutic Effect of Intense Pulsed Light in Patients with Sjögren’s Syndrome Related Dry Eye. Journal of Clinical Medicine, 11(5), 1377. https://doi.org/10.3390/jcm11051377

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