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Superior Limbic KeratoconjunctivitisNCT03731624

Diadenosine Polyphosphates and Mucin Associated With Ocular Surface Disorders

An observational study of Superior Limbic Keratoconjunctivitis and Dry Eye Syndromes, run by Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation at 1 site in Taiwan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Dry eye disease, ocular graft-versus-host disease (GVHD), and superior limbic keratoconjunctivitis (SLK) are all ocular surface disorders which mostly involve the outer surface of the eye. Many of the ocular surface disorders may result from or be aggravated by the mechanical stress from eyelid blinking. Read more about this study

Who is it for?
Ages 18 to 99 yearsHealthy volunteers can take part
How many people
50 participants
Where
1 siteTaiwan
Study dates
1 Jan 2018to 31 Dec 2023
How long will I take part?
3 Years
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: This study will have recruit 40 patients with ocular surface disorders (20 dry eye patients, 10 ocular GVHD patients, and 10 SLK patients) and 10 normal subjects. Tear samples and questionnaires before and after treatment (bandage soft contact lens application) will be collected.

Who may be able to join

  • age 18 years or older
  • diagnosis of dry eye disease, ocular GVHD, and SLK
  • patients who ever received topical medications, including artificial tears and topical steroids, at least 3 months, but refractory to the treatment
  • absence of new systemic immunosuppressive medications within 1 month

Who cannot join

  • pregnancy
  • absolute neutrophil count less than 1000/mL
  • known hypersensitivity or allergy to contact lens care products
  • treatment with scleral lenses within the previous 3 months
  • evidence of any active infection in the eyes
  • receiving any ocular surgeries within the previous 3 months

Trial locations and contacts

1 site in 1 country.

Taiwan1 site, 1 recruiting
  • Taipei Tzu Chi Hospital

    New Taipei City, 231

    Yi-Chen Sun, MD, PhD, +886266289779 ext. 1220, yichensun.tzuchi@gmail.com

    Recruiting

Other trials in Taiwan

About this study

Official title: The Expression Levels of Diadenosine Polyphosphates and Mucin in Mechanical Stress-related Ocular Surface Disorders

Dry eye disease, ocular graft-versus-host disease (GVHD), and superior limbic keratoconjunctivitis (SLK) are all ocular surface disorders which mostly involve the outer surface of the eye. Many of the ocular surface disorders may result from or be aggravated by the mechanical stress from eyelid blinking. Specifically, SLK is an inflammatory ocular surface disorder characterizing by redundant superior bulbar conjunctiva. Since redundant superior bulbar conjunctiva can cause a significant mechanical force during eyelid blinking, we found that conjunctival resection with Tenon's capsule excision is helpful in relieving the symptoms of SLK patients. Therapeutic contact lens, protecting the ocular surface from the microtrauma between eyelid and ocular surface, is also an effective treatment for severe dry eye disease, ocular GVHD, and SLK. Although shearing force/mechanical stress has been studied in many different tissues and disease entities, the impact of shearing force over ocular surface is still unclear.

While the importance of mechanical stress in ocular surface disorder has been reported, the specific molecule involving the pathogenesis is still unknown. Diadenosine polyphosphates are a family of dinucleotides. They can enhance tear secretion and increase corneal wound healing rate from previous reports. Shear-stress stimuli was also noted to be able to induce diadenosine polyphosphates releasing from human corneal epithelium. In addition, mucin, one of the three components of tear film, has been greatly emphasized in the pathogenesis of dry eye disease. There are also some reports about the shearing force compensating the mucin contents in the inflammatory lung/bowel diseases. If diadenosine polyphosphates or mucin indeed play a role in mechanical stress-related ocular surface disorders, it will be a promising therapeutic targeting in the future.

Read the detailed description

Ocular surface disorders are diseases involving the most outer surface of the eyeball - the transparent layers that forms the front of the eye, including cornea and conjunctiva. One of the most common ocular surface disorders is dry eye disease (DED) which has a great impact on patients' quality of life. In addition, ocular graft-versus-host disease (GVHD) and superior limbic keratoconjunctivitis (SLK) are also ocular surface disorders affecting patients' quality of life significantly.

  1. Great impact of ocular surface disorders on quality of life 1.1. Impact of dry eye disease Dry eye disease (DED) is a common ocular surface disorder. Vision-related quality of life in dry eye patients is impaired and is correlated with anxiety and depression.1 Patients with DED are often evaluated by a symptom scale called ocular surface disorder index (OSDI). The OSDI is a valid and reliable scale for diagnosis and measurement of the severity of DED or other ocular surface disorder. It is also a convenient option for clinical use as a result of its shorter completion time. 1.2. Impact of GVHD GVHD caused by alloreactive donor T cells is an important cause of nonrelapse mortality and morbidity after allogeneic hematopoietic cell transplantation (HCT). Ocular GVHD reportedly occurs in more than 50% of allogeneic HCT recipients with chronic GVHD. It can affect all parts of the eye, but the ocular surface is the most common level of involvement. Yoshi et al suggested strong correlations of serial changes in the NIH eye score, the OSDI, and the Lee eye subscale. Given that the OSDI consists of 12 items instead of the 3 for the Lee eye subscale, they found little basis for recommending the OSDI to measure change in the activity of ocular GVHD. Therefore, the Lee eye subscale might be a good choice for determining the impact of ocular GVHD on quality of life. 1.3. Impact of SLK SLK is an ocular surface disorder characterized by unilateral or bilateral redundancy of the superior bulbar conjunctiva with inflammation of the superior tarsal and bulbar conjunctiva. There are many patients suffering by the symptoms of SLK because of its unclear etiology and no standard treatment. In addition, SLK is not easy to make a definite diagnosis, the impact of SLK on quality of life could be underestimated.
  2. Mechanical stress from eyelid blinking may be an aggravating or contributing factor of ocular GVHD and SLK 2.1. The symptoms of ocular GVHD relieved by bandage soft contact lens (BSCL) application via the isolation from mechanical stress (eyelid blinking) and ocular surface The standard treatment of ocular GVHD is still not in consensus. Because of the immune reaction participating in the pathogenesis of ocular GVHD, some topical immunosuppressants, such as cyclosporine A (CsA) and tacrolimus, are applied on the patients with ocular GVHD. Allogeneic serum eye drops and autologous plasma rich in platelet-derived growth factor (PDGF) eye drops were also reported to be effective in chronic ocular GVHD patients. For medication refractory cases, punctal plugs, scleral lens, and bandage soft contact lens (BSCL) could be applied as alternative treatments for ocular GVHD patient. According to previous report, BSCL is a safe and effective treatment option that improves manifestations of ocular GVHD. BSCL can act as a barrier to further epithelial disruption and corneal nerve stimulation by the shearing force of the upper lid during the blink. 2.2. Mechanical stress plays a role in the pathogenesis of SLK Mechanical stimulation may contribute to the pathogenesis of SLK. We speculated that this kind of physical trauma not only results in the keratinization of conjunctival epithelium, but also induced inflammatory cells and mediators, such as mast cells and cytokines, respectively. Three out of 8 SLK patients benefitted from large diameter contact lens application. Conjunctival resection with Tenon's capsule excision was also reported as a beneficial treatment for medication refractory SLK patients.
  3. The expression of diadenosine polyphosphates and mucin may alter the clinical presentation or diagnosis of ocular surface disorders 3.1. Dinucleoside polyphosphates in ocular surface disorder Diadenosine polyphosphates are a family of dinucleotides, consisting of two adenosine nucleosides joined by a phosphate chain whose length can vary from 2 to 7 phosphates. They are released from nerve terminals to the extracellular milieu where they can exert actions by interacting with purinergic receptors. Since the levels of diadenosine tetraphosphate (Ap4A) and diadenosine pentaphosphate (Ap5A) in tears were found to be greater in all dry eye patients, these compounds could be objective markers to score dry eye. In the forced blink experiments, concentrations of the diadenosine polyphosphates rose with increasing blink frequency.13 In addition, topical application of diadenosine tetraphosphate was also noted to be able to stimulate tear secretion in vivo. Because of the higher levels of Ap4A found in refractive surgery patients during the first day after the surgery, this dinucleotide release might help in the wound healing process as well. 3.2. Mucin in ocular surface disorder Mucin plays an important role over the ocular surface. It converts the hydrophobic corneal surface to a hydrophilic surface by adhering to the glycocalyx on the corneal microvilli. It also contributes differently to the protection of the ocular surface against allergens, pathogens, extracellular molecules, abrasive stress, and drying. MUC1 (mucin 1), 2, 4, 5AC, and 7 are the subtypes of mucin that can be found over ocular surface, including cornea, conjunctiva, goblet cell, and lacrimal gland. Ocular surface pathologies, i.e. dry eye syndrome or allergic conjunctivitis, are reportedly associated with alteration of expression pattern of mucin components. Although dryness of the ocular surface is a fundamental situation, local inflammation in the epithelium plays critical roles in the pathogenesis and symptom in patients with dry eye syndrome. Mucin deficiency can lead to inflammation in the ocular surface. Expression of MUC1, MUC2, MUC4, and MUC5AC are significantly lower in conjunctival epithelium gathered by impression cytology in the patients with dry eye syndrome compared with that in normal subject.18 Reduction of MUC1 expression in dry eye local tissue is reportedly most prominent and could be a marker for diagnosis or evaluation of the disease severity. Topical eye drop of Rebamipide, a drug that is capable of stimulating of mucin secretion in gastrointestinal tract or conjunctiva, is approved in Japanese government for use in the treatment of dry eye diseases. Mucin was also reported as an important factor contributing to some allergic keratoconjunctivitis. In the patients with atopic keratoconjunctivitis, expression of goblet cell-specific mucin, MUC5AC mRNA, was reduced and MUC16 mRNA expression was upregulated in brush cytology specimens. Besides, patients with vernal keratoconjunctivitis had increased numbers of conjunctival goblet cells from impression cytology specimen. This phenomenon also altered the levels of mucin over the ocular surface.
  4. Mechanical stress can violate the levels of diadenosine polyphosphates and mucin 4.1. Diadenosine polyphosphate under mechanical stress It is known that cells under stress accumulate various dinucleoside polyphosphates, compounds suggested to function as alarmones. The release of diadenosine polyphosphates to the tears can be caused by shear stress, such as that corneal epithelial cells release these molecules as a consequence of the lid contact during the blinking process. Daily wear of rigid gas permeable lenses also can increase the levels of Ap4A due to mechanical stimulation by blinking of the corneal epithelium, and this is associated with discomfort.

4.2. Mucin under mechanical stress Gastrointestinal tract and upper airway are the organ systems filled with mucin as an important protection. MUC1 and MUC4 in the colon and MUC3 in the duodenum were upregulated in stressed animals. These findings suggest that chronic stress may affect mucin expression in the gastrointestinal tract. In addition, human bronchial epithelial cell cultures (HBECCs) are very sensitive to the mechanical stress associated with handling and pipetting. Mucin secretion at baseline in vivo occurs in a mechanically dynamic lung environment: goblet cells are exposed continuously to mechanical forces, shear stress and compressive stress, that may stimulate and/or influence the production and secretion of mucins.

Medical subject headings
Dry Eye Syndromes, Graft vs Host Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03731624
Study groupRoleWhat they receive
SLKNot described
GVHDNot described
Dry eyeNot described
ControlNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. adenosine polyphosphate level before treatment

    identify the levels of adenosine polyphosphate via High Performance Liquid Chromatography (HPLC) between groups

    Measured: before treatment

  2. mucin level before treatment

    identify the levels of mucin via ELISA between groups

    Measured: before treatment

Secondary outcomes (2)
  1. adenosine polyphosphate after treatment

    identify the levels of adenosine polyphosphate via HPLC between groups

    Measured: post-treatment one month, three months and six months

  2. mucin after treatment

    identify the levels of mucin via ELISA between groups

    Measured: post-treatment one month, three months and six months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Nov 2018
  2. Study start1 Jan 2018
  3. Primary completion31 Dec 2020 (estimated)
  4. Study completion31 Dec 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
Target duration
3 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT03731624
Sponsor's protocol ID
TCRD-TPE-107-07
Status last verified
Nov 2018
First submitted
11 Oct 2018
Last updated
6 Nov 2018
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Superior Limbic Keratoconjunctivitis and Dry Eye Syndromes, run by Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 6 Nov 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yi-Chen Sun, MD, PhD (+886266289779 ext. 1220, yichensun.tzuchi@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

adenosine polyphosphate level before treatment (time frame: before treatment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2018.

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