LED therapy is the future gadget for vaginal atrophy in postmenopause

Kim S1

Research Type

Clinical

Abstract Category

Continence Care Products / Devices / Technologies

Abstract 637
Open Discussion ePosters
Scientific Open Discussion Session 105
Thursday 24th October 2024
13:45 - 13:50 (ePoster Station 5)
Exhibition Hall
Quality of Life (QoL) Sexual Dysfunction Female
1. Catholic kwandong university college of medicine, International St. Mary's hospital
Presenter
Links

Poster

Abstract

Hypothesis / aims of study
Genital atrophy is the most important problem in postmenopausal women. It makes to decrease the quality of life including genital dryness, itching sense and female sexual function. Our study evaluate the change of collagen change using Light emitting diode (LED) treatment in mouses as a preclinical study and in postmenopausal women as a clinical study.
Study design, materials and methods
We performed a prospective evaluation of 18 postmenopausal mouses (control group; n=9, LED group; n=9) which were undergone bilateral ovariectomy from July 2021 to September 2021. We used to the mixed wavelengths of three types as the 460-nm LED (blue), the 592-nm LED (amber), the 630-nm LED (red). Each mouse got LED device (Bellalux®, Linkoptics, Gwangu, Korea) on its buttock for 20 minutes for 2weeks. We got the 1*1cm tissue on both buttock and analyzed to immunohistochemistry analysis using Masson trichrome (MT), hematoxylin and eosin (H&E), smooth muscle antibody (SMA) and vimentin stain. Our study was approved by the experimental animal institutional review board under registration number CKU-02-2021-004. Also 10 women with genital atrophy in postmenopause were enrolled to our hopspital in from June 2022 to December 2022. They used portable LED device (Luminiel Y®, Linkoptics, Gwangu, Korea) the mixed three types of wavelengths during 4 weeks. Our study was approved by the institutional review board under registration number S22SSSE0022. On surgeon evaluated to subjective symptoms and their sexual function via FSFI as validated questionairres Data were analyzed using SPSS software (version 22; IBM Corp., Armonk, NY, USA). Statistical significance was considered as P< 0.05). The paired t-test analysis was analyzed.
Results
We compared to the result of blood test between no LED group (n=10) and LED therapy group (n=10) for 2 weeks after LED treatment. We compared to the collagen density and the fibroblast count between no LED group (n=9) and LED therapy group (n=9) for 4 weeks after LED treatment. On MT stain, mean scale of no therapy group was 127.28 ± 5.03 to be increased to 102.06 ± 6.94 of the LED therapy group (p<0.05). The scale range on MT stain is from 0 to 250; 0 scale means the thickest density of collagen. We check the fibroblast count by eyeball evaluation in each section. The fibroblast count was increased from 51.19 ± 14.71 (control group) to 80.22 ± 31.28 (LED therapy group) after treatment (p<0.05). After 1 months later, their subjective symptoms were improved (p<0.05). Desire and Arousal got a good score (p<0.05).
Interpretation of results
The collagen denstity of LED thearpy group was more thicker than control group in preclinical study. The fibroblast count was increaesed to buttock after  LED treatment . LED was effective cure to  collgen defect in postmenopause. In clinical study,  LED therpy was effective to recovery with genital atrophy.
Concluding message
LED was  promoted collagen regeneration in mouse model. Postmenopausal atrophy is caused by collagen loss. It is expected that genital atrophy would a good option for adequate treatment to restore in urogynecologic function and anatomical structure.
References
  1. Fernanda A. Ana L.R. V De´lio MC, and Lu´cia CP. The effect of vaginal erbium laser treatment on sexual function and vaginal health in women with a history of breast cancer and symptoms of the genitourinary syndrome of menopause: a prospective study. Menopause.2019; 26[9]; 1052-1058
  2. Margit L.W. Juhasz, MD,Dorota Z. Korta. and Natasha AM. Vaginal Rejuvenation: A Retrospective Review of Lasers and Radiofrequency Devices. Dermatologic surgery. 2021; 47[4]; 489-494
Disclosures
Funding This research was supported by the technology transfer and commercialization Program through INNOPOLIS Foundation funded by the Ministry of Science and ICT (2021-GJ-RD-0146). / The portable LED device for Y zone care) Clinical Trial No Subjects Human Ethics Committee International St. mary's hospital institutional ethical board Helsinki Yes Informed Consent Yes
21/03/2025 17:00:17