Role of Omega-3 fatty acids in
meibomian gland dysfunction
Jain C.1, Malik V.K.2, Bowry R.3
1Dr. Charu Jain, Associate
Professor, 2Dr. V.K. Malik, Professor & HOD, 3Dr. Rohan
Bowry, JR-3, all authors are affiliated with Subharti Medical College, Meerut (U.P.)
India.
Corresponding Author: Dr. Charu Jain, Associate Professor,
Department of Ophthalmology, Subharti Medical College, Meerut, U.P. E-mail id- cjsubharti@rediffmail.com
Abstract
Objective: To evaluate the role of omega-3 fatty acids in meibomian
gland dysfunction (MGD). Design:
This was a prospective randomized control study that included patients with MGD
attending outpatient Department of Ophthalmology, Subharti Medical College,
Meerut. Subjects: 40 patients of
both sex above 40 years of age with MGD were included in the study. Methods: Age matched randomization of
patients was done in two groups of 20 each. Patients in group A were given 2
capsules of 300mg omega-3 fatty acids for 12 weeks while patients in group B
were given a placebo oral supplement. Patients were examined at one-month
interval for 3 months after the initial visit. At each visit Ocular Surface
Disease Index (OSDI), Schirmer test, Tear film break up time (TBUT), Fluroscein
staining and meibum quality score was evaluated. Results: After 3 months we found statistically significant
improvement in subjective as well as objective parameters of group A patients
(p value < .05) as compared to group B patients. Conclusion: Thus, dietary supplementation with omega-3 fatty acids
is an effective treatment modality in meibomian gland dysfunction (MGD).
Keywords: Meibum quality score, Meibomian gland dysfunction (MGD), Omega-3
fatty acids, Ocular Surface Disease Index.
Author Corrected; 23th October 20178 Accepted for Publication: 29th October 2018
Introduction
Meibomian gland
dysfunction (MGD) is one of the most common causes of patient complaints in a
comprehensive ophthalmology practice [1]. It is often difficult to distinguish
the cause as there is a considerable overlap between blepharitis, MGD and dry
eye [2]. Generally, the prevalence of MGD is higher in Asian population ranging
from 46% to 70%, whereas in Caucasian population it ranges from 3.5% to 20%
[3]. According to the International workshop on MGD, MGD is a chronic diffuse
abnormality of the meibomian gland characterized by terminal duct obstruction
and/or qualitative/ quantitative changes in the glandular secretion [3]. It may
result in alteration of the tear film, symptoms of irritation, clinically
apparent inflammation and ocular surface disease [4].
Healthy meibum is
essential for a healthy ocular surface as it constitutes to tear film stability
and also provides a smooth optical surface at the air-tear interface [5]. In
MGD, meibum is often abnormal progressively changing in colour from clear to
yellow and in consistency from liquid to toothpaste like. Studies have
demonstrated that alteration in meibum in MGD results in production of toxic
tear film destabilizing components such as fatty acids [6,7].
Additionally, ductal hyperkeratinization may result in blockage of the duct
orifice and stagnation of meibum.
Inflammation is also an
integral component of MGD. Increased expression of conjunctival markers of
inflammation and proinflammatory mediators like cytokines and interleukins have
been demonstrated in tear film of dry eye and MGD patients [8,9].
This inflammatory process ultimately disrupts the normal homeostatic functional
unit responsible for normal tear production.
Omega-3 and omega
polyunsaturated essential fatty acids are precursors of lipid mediators known
as eicosanoids that play an important role in regulating inflammation [10].
Omega-3 fatty acid eicosapentaenoic acid (EPA) and omega-6 fatty acid arachidonic
acid compete for the same enzyme at the level of cycloxegenase and lipoxygenase
pathway [11]. The anti-inflammatory action is believed to result
from the synthesis of prostaglandin E3 and leukotriene B5 from EPA that inhibits
the conversion of arachidonic acid to potentially harmful mediators prostaglandin
E2 and leukotriene B4. The two best sources of omega-3 fatty acids are flaxseed
and cold water dark fish (salmon, tuna etc).
There are two hypothesis
as to why dietary supplementation of omega-3 fatty acids may alleviate
blepharitis and the resulting MGD and dry eye symptoms. The first hypothesis
relies on the fact that the breakdown of omega-3 fatty acids results in the
production of molecules that suppress inflammation, whereas the breakdown of
omega-6 fatty acids result in the molecules that can lead to inflammation [10].
The second hypothesis regards the composition of tear. It has been suggested
that an unstable tear film results from abnormal meibomian gland secretions and
can in evaporative dry eye. Supplementing the diet with high amounts of omega-3
fatty acids is likely to change the fatty acid composition and therefore the
properties of meibomian gland secretions. This change may be beneficial in tear
stabilization and may prevent the inflammation from blocking the meibomian
gland ducts and meibum stagnation [11].
Although MGD rarely
threatens sight, it is a troublesome and symptomatic condition. Patients
usually present with burning, watering, foreign body sensation, itching,
erythema of lids and changes in eyelashes. The condition most typically has a
chronic course with intermittent exacerbations of symptomatic disease. Many
patients move from one doctor to another seeking relief from their symptoms.
Purpose of this study- The current treatment modalities for
MGD include lid hygiene, warm compresses, artificial tears, topical
antibiotic/steroid combination and systemic antibiotics which provide only
temporary symptomatic relief. So, the present study has been undertaken to
evaluate the role of omega-3 fatty acids in meibomian gland disease.
Material
Methods
Study Design- This prospective randomized control study was
conducted in Department of Ophthalmology, Subharti Medical College, Meerut
between January 2018 and June 2018. It was performed after the approval of the
institutional committee and an informed consent was taken from all the patients
prior to the study.
A total of 40 patients of
either sex above 40 years of age diagnosed with MGD and fulfilling the
inclusion criteria were included in the study.
Sampling Method- Age matched randomization of patients
was done in two groups of 20 each.
Group A- Patients were given Omega-3 fatty acids in recommended dose (2 capsules of 300 mg Omega-3 fatty
acids twice a day for 12 weeks).
Group B- Patients were given a placebo oral supplement for 12 weeks.
Inclusion criteria- Patients above 40 years diagnosed
with MGD according to criteria identified at 2011 International workshop on MGD
[12].
Exclusion criteria
1. Active ocular infection
or other allergic disorders.
2. Contact lens wearers
3. Ophthalmic laser
treatment
4. Previous history of
herpetic keratitis
5. Degenerative corneal
disease.
6. Pregnant and lactating
females.
7. Patients on systemic
drugs like beta blockers, anti-cholinergics, anticoagulants etc.
8. Patients with other
systemic diseases like increase bleeding tendency.
Clinical Examination- A detailed clinical history including
age, sex, occupation, hormonal therapy, oral vitamin A treatment as well as
history of systemic diseases like diabetes; hypertension or hyperthyroidism was
taken from all the patients. At each visit, subjects were asked to complete the
Ocular Surface Disease Index OSDI, an established measure of patient dry eye
symptoms [12]. A score of 0 to 12 indicates a normal eye, 13 to 22 mild dry
eye, 23 to 32 moderate dry eye and over 33 indicates severe dry eye. Thus, a
decrease in OSDI score indicates improvement.
At each visit complete
ocular examination including visual acuity, intraocular pressure measurement and
fundus examination was done. Objective clinical measures included tear
production (Schirmer I with anesthesia), tear film stability (fluorescein Tear
film break up time TBUT), ocular surface health (fluorescein staining) and
meibomian gland health (meibum quality).
The Schirmer I test was
performed with anesthesia. After instillation of topical anesthetic drops,
Schirmer strip was placed in the lower fornix at the junction of lateral third
and medial two thirds. The strip was removed after 5 min and a measurement of
wet area of the strip was done.
Fluorescein TBUT was
performed by touching a fluorescein strip to the inferior palpebral conjunctiva.
Patients were asked to blink several times to mix the fluorescein with the tear
film. They were then asked to open their eyes and not to blink and the time
between the opening of the eyes and the appearance of first dry spot was
measured in seconds. It was repeated three times and the average was taken as
final TBUT.
Fluorescein ocular
staining was performed by evaluating the corneal fluorescein stain 1 minute
after fluorescein instillation by observing the cornea through a cobalt blue
light. Corneal staining was graded using a scale of 0-3 (absent to diffuse) for
5 corneal regions. The final score was determined by totaling all individual
scores for each eye.
The lid margin, lashes and
meibomian glands were examined on slit lamp. Scoring of meibum character and
colour was done as shown in table 1. A score of greater than 1.5 indicates
healthy meibum.
Table-1: Meibum Character and Color Scores
Character Score |
Description |
0 |
Fluid |
1 |
Thickened |
2 |
Granular(particulates
visible) |
3 |
Toothpaste like |
Color Score |
Description |
0 |
Clear |
0.5 |
Yellow |
1 |
White |
Follow Up- Follow up of patients was
done at 1,2 and 3 months after the initial visit. At each visit complete ocular
examination was done including Ocular Surface Disease Index (OSDI), Schirmer 1
Test, Tear film break up time (TBUT), Corneal fluorescein staining and Meibum
quality score.
Statistical Analysis- Statistical analysis was done using
Microsoft Access database. Comparison between randomized groups was done using
paired t test and p value < 0.05 was taken as statistically significant.
Results
Out of 40 patients
recruited in the study, 38 patients completed the study. The mean age of
patients was 49.36 years and majority of them were females (25 out of 38).
Disease was bilateral in all patients.
There was no significant
difference in baseline symptoms and signs in the two groups. Throughout the
study, the investigators and patients were blinded to the treatment
assignments.
Table-2: Patient characteristics at baseline
Variable |
Group A(Omega-3 FA) |
Group B (Placebo) |
OSDI Score (0-100) |
36.3 ± 16.1 |
35.8 ± 22.5 |
Schirmer Score (mm) |
5.84 ± 2.3 |
5.92 ± 1.7 |
TBUT (sec) |
5.95 ± 0.76 |
5.88 ± 0.94 |
Fluorescein Staining
(0-15) |
2.2 ± 2.6 |
2.3 ± 1.5 |
Meibum Quality Score
(0-4) |
2.7 ± 0.9 |
2.5 ± 0.79 |
Table-3: Patient Characteristics At 3 months
Variable |
Group A (Omega-3 FA) |
P value |
Group B (Placebo) |
p value |
OSDI Score (0-100) |
15.7 ± 13.6 |
0.005 |
30.6 ± 12.8 |
0.4 |
Schirmer Score (mm) |
10.94 ± 3.6 |
0.02 |
6.10 ± 1.3 |
0.5 |
TBUT (sec) |
8.8 ± 1.2 |
0.007 |
6.7 ± 0.14 |
0.2 |
Fluorescein Staining
(0-15) |
2.04 ± 1.4 |
0.3 |
2.01 ± 0.48 |
0.6 |
Meibum Quality Score
(0-4) |
1.1 ± 0.46 |
0.02 |
2.1 ± 1.2 |
0.2 |
In our study, the patients
supplemented with Omega-3 fatty acid noted a marked decrease in their symptoms
at every visit. At 3 months the overall OSDI scores significantly improved in
Group A patients (p = 0.005) as compared to Group B patients (p = 0.4).
Group A patients also
showed a marked improvement in Schirmer score (p = 0.02) and TBUT (p = 0.007)
at 3 months. On the contrary no significant improvement was seen in Group B
patients (p >0.05). However, fluroscein staining showed no significant
change in both the groups at 3 months (p value >0.05).
The health of the
meibomian glands and their secretions also showed a marked improvement in Group
A. At 3 months, the average meibum quality significantly improved from granular
at baseline to thickened or fluid and colour from white or yellow to clear in
Group A (p = 0.02 ). No significant improvement was seen in Group B patients
(p=0.2).
Discussion
There has been great
interest over the past decade in the role of dietary supplements in the
management of meibomian gland dysfunction and the resulting dry eye. Current
drug therapies have many side effects and do not offer a long-term satisfactory
treatment. Thus, many patients move fruitlessly from doctor to doctor to seek a
satisfactory solution to the problem.
Recently experimental
studies have provided evidence that dietary supplementation of Omega-3 fatty
acid modifies inflammatory and immune reactions making them potential
therapeutic agents for inflammatory and autoimmune diseases. Omega-3 FA results
in competitive inhibition of Omega-6 FA reducing the levels of inflammatory
arachidonic acid oxidation products with formation of less active prostanoids
[10]. Thus, Omega-3 fatty acids reduce overall inflammatory state of eyelid
margin and meibomian glands.
To determine the effect of
dietary supplementation with omega-3 fatty acids on MGD, we conducted a
prospective randomized control study where 40 patients with MGD were randomly
assigned to either the omega-3 or placebo group. In our study, we evaluated
subjective symptoms as well as objective signs in order to define the possible
role of Omega-3 fatty acids in MGD. We found that Omega-3 FA’s not only
alleviates the patients symptoms but also improves the clinical markers of MGD
as evidenced by positive drift in OSDI score, Schirmer score, TBUT and meibum
quality score. None of the patients in our study reported any adverse effect of
Omega-3 FA. The only demerit is that that the drug is costly due to which some
patients cannot afford it for long time.
Pinna et al. conducted a
similar study in fifty seven patients with MGD and found that oral therapy with
linoleic and linolenic acid along with eyelid hygiene improves symptoms and
reduces eyelid margin inflammation in MGD more than either omega-6 FAs or
eyelid hygiene alone [11].
Wojtowicz et al. concluded
that dietary supplementation with Omega-3 FAs in MGD and dry eye showed no
significant effect on meibum lipid composition or aqueous tear evaporation rate
[13]. On the other hand, the average tear production and tear volume was
increased in the omega-3 group as indicated by Schirmer test and
fluorophotometry.
Olenik A et al. conducted
a randomized double mask trial to evaluate the effect of Omega-3 FAs
supplementation in MGD and found that oral Omega-3 FAs, 1.5 grams per day are
beneficial as an adjunctive treatment of MGD, mainly by improving tear
stability [14].
Macsai et al conducted a
prospective randomized placebo controlled masked trial to evaluate the role of
Omega-3 dietary supplementation in patients with blepharitis and MGD [15]. This
trial demonstrated a decrease in the RBC and plasma ratios of Omega-6 to
Omega-3 in patients taking Omega-3 dietary supplementation, as compared to
controls, and improvement in their overall OSDI score, TBUT and meibum score.
This study was the first to demonstrate an induced change in the fatty acid
saturation content in meibum as a result of dietary supplementation with
Omega-3 fatty acids.
Epitropoulos et al.
demonstrated a significant improvement in dry eye symptoms from baseline with
the oral ingestion of re-esterified omega-3 supplements for 12 weeks compared
with those taking a control. The improvement of many of the signs were seen as
early as 6 weeks suggesting a rapid response to nutritional therapy [16].
Opitz et al. suggested
that if older patients were identified and treated before they became
symptomatic, end-stage disease or MG atrophy may not occur [17]. Summerton
suggested that Omega-3 dietary supplementation for blepharitis and MGD may
decrease the red blood cell and plasma ratios of omega-6 to omega-3 and improve
the overall ocular surface index score, TBUT and meibum score [18].
Nagpal et al. conducted a
randomized control study to study the effects of Omega-3fatty acids in patients
with meibomian gland dysfunction. After 3 months, they found statistically
significant improvement in mean OSDI, TBUT, Rose Bengal staining and Schirmer
test. Thus they concluded that oral omega-3 fatty acids 1g per day is
beneficial in the treatment of MGD [19]. Saif AT studied the role of oral
linolenic acid dietary supplementation in posterior blepharitis and meibomian
gland dysfunction. He found significant improvement in dry eye symptoms, TBUT,
Schirmer test and meibomian gland orifices after 3 months and concluded that oral
linolenic acid (omega-3 fatty acids) is effective in treatment of moderate to
severe chronic blepharitis and MGD [20].
In our study also we found
statistically significant improvement in OSDI score, TBUT, Fluorescein staining
and meibum quality score 3 months after oral omega-3 fatty acids. Thus, this
study supports the role of inflammation in etiology of MGD and suggests that
Omega-3 FA’s may improve tear film stability and prevent the inflammation of
lid margin, meibomian gland ducts and meibum stagnation.
Despite affecting millions
and altering the quality of life the current treatment modalities for MGD are
palliative and provide only temporary symptomatic relief. But with the better
understanding of underlying pathophysiological process of disease, systemic
omega-3 fatty acids have been found to have a positive effect on MGD by
subsiding vicious cycle of ocular inflammation
Conclusion
We conclude that dietary
supplementation with Omega-3 FA’s either as an alternative or as an adjunct
therapy holds great promise in the treatment of meibomian gland dysfunction and
the resulting evaporative dry eye disease. Although the results of our study
are encouraging but our study has certain limitations. The sample size is
relatively small and follow up period is also short. So further work with a
larger sample size and long term follow up is warranted to access the efficacy
and safety of oral Omega-3 FA’s in patients with meibomian gland dysfunction.
Contributions
·
Dr. Charu Jain– central idea behind the study, main author of
this study, workup and complete evaluation of all patients.
·
Dr. V.K. Malik– arranged free medications for the patients
included in study and also guided at each step during the study process.
·
Dr. Rohan Bowry– helped in workup of patients, along with
compilation of data and its statistical analysis
References