<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJOph</journal-id><journal-title-group><journal-title>Open Journal of Ophthalmology</journal-title></journal-title-group><issn pub-type="epub">2165-7408</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojoph.2017.72014</article-id><article-id pub-id-type="publisher-id">OJOph-76229</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prevalence of Dry Eye Disease in a Rural Niger Delta Community, Southern Nigeria
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>A.</surname><given-names>A. Onua</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>I.</surname><given-names>O. Chukwuka</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Surgery, University of Port Harcourt, Port Harcourt, Nigeria</addr-line></aff><pub-date pub-type="epub"><day>14</day><month>04</month><year>2017</year></pub-date><volume>07</volume><issue>02</issue><fpage>95</fpage><lpage>102</lpage><history><date date-type="received"><day>February</day>	<month>28,</month>	<year>2017</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>May</month>	<year>15,</year>	</date><date date-type="accepted"><day>May</day>	<month>18,</month>	<year>2017</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Dry Eye Disease (DED) or Dry Eye Syndrome (DES) is the fast growing public health problem characterized by deficiency in the quantity and/or quality of tear film due to tear deficiency or excessive tear evaporation. It negatively affects the health and the quality of life of individuals. Although dry eye is a common eye disease world-wide, many people are undiagnosed and untreated especially in underdeveloped countries. Aim: To determine the prevalence of dry eye disease in Aluu community. Methods: The cross-sectional, population-based study from 16th to 18th June 2016. Participants were members and residents of the community who consented to ocular examinations. Ocular examinations including Schimer’s test were carried out. Data were entered into a spread sheet using statistical package for social sciences (SPSS) 16.0 statistical software and subsequently analysed. Results: Seven hundred and thirty persons (210 males and 520 females) participated in the study. The mean age was 34.2 &#177; 12.4 years. The prevalence of Dry Eye Disease in this study was 27.4%. Over 72% of the study population had normal Schimer’s test 95% CI [15.0 - 15.2], 18.4% had mild dry eye syndrome 95% CI [10.1 - 10.7], 6.8% had moderate dry eye syndrome test 95% CI [5.5 - 7.6] while 2.2% had severe dry eye syndrome test 95% CI [3.0 - 3.8]. Conclusion: The prevalence of dry eye disease in Aluu community is high. It is therefore, advocated special eye healthcare intervention by governments and non-governmental agencies be extended to this rural Niger Delta community.
 
</p></abstract><kwd-group><kwd>Dry Eye Disease</kwd><kwd> Prevalence</kwd><kwd> Rural Niger Delta Community</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Dry Eye Disease is an established chronic ocular surface disease and a growing public health problem seen by eye care practitioners [<xref ref-type="bibr" rid="scirp.76229-ref1">1</xref>] . According to the International Dry Eye Workshop 2007 (DEWS), dry eye is defined as a multifactorial disease affecting tear and the ocular surface with resultant ocular discomfort, blurring of vision, accompanied by increased tear osmolarity and ocular surface inflammation [<xref ref-type="bibr" rid="scirp.76229-ref2">2</xref>] .</p><p>Dry Eye Disease (DED) is characterized by deficiency in the quantity and/or quality of tear film due to tear deficiency or excessive tear evaporation which causes damage to the ocular surface and is associated with symptoms of discomfort, ocular irritation, dryness and fluctuating visual disturbances, burning sensation, foreign body sensation, grittiness, itching of the eyes, and stinging feeling, pain, soreness, blurry vision, strain and photophobia [<xref ref-type="bibr" rid="scirp.76229-ref3">3</xref>] . These symptoms often have the negative impact on physical, social and psychological health as well as overall sense of well-being of the individual [<xref ref-type="bibr" rid="scirp.76229-ref4">4</xref>] . Wider consequences to dry eye disease are also evident, with reports of anxiety and depression associated with the condition and low Quality of life (QoL) [<xref ref-type="bibr" rid="scirp.76229-ref5">5</xref>] .</p><p>Although the aetiology of Dry Eye Disease (DED) is still largely unknown, some of the risk factors have been identified. Dry eye diseases can be secondary to environmental, hormonal, physiological, contact lens wear and pathological causes [<xref ref-type="bibr" rid="scirp.76229-ref6">6</xref>] . With pathological causes, both the tear deficiency type and evaporative type can lead to the dry eye syndrome. Systemic diseases such as diabetes, thyroid disease, rheumatoid arthritis, systemic lupus etc. can also lead to dry eyes [<xref ref-type="bibr" rid="scirp.76229-ref6">6</xref>] . In addition, patients with previous eye surgeries or regular use of eye medications or systemic medications can be predisposed to dry eyes. Many systemic medications, such as antihistamines, antidepressants, beta-blockers and oral contraceptives can also be associated with dry eyes [<xref ref-type="bibr" rid="scirp.76229-ref6">6</xref>] .</p><p>The diagnosis of dry eye is not straightforward due to its multifactorial nature of aetiology [<xref ref-type="bibr" rid="scirp.76229-ref7">7</xref>] . Many clinical tests such as tear break-up time, corneal staining, meibomian gland digital expression, tear osmolarity, Schirmer test and assessment of the symptoms using ocular surface disease index (OSDI) have been employed by various authors. However, there is so far no consensus on a gold standard diagnostic criterion. In many cases, symptoms and signs do not correlate well with each other. Ohashi reported that, symptoms of dry eye disease, Schirmer tests (&lt;5 mm after 5 mins) and clearance test (&lt;8&#215;), fluorescein stain and Rose Bengal staining (&gt;3+) qualify as clinical diagnosis of dry eyes [<xref ref-type="bibr" rid="scirp.76229-ref6">6</xref>] .</p><p>In this study, the Schimer 1 test was used leveraging on its applicability in an epidemiological survey, speed of use, low cost and convenience. Although dry eye is a common eye disease world-wide, many people with dry eyes however, remain undiagnosed and untreated especially in underdeveloped countries [<xref ref-type="bibr" rid="scirp.76229-ref8">8</xref>] . In US, as many as 6% of the population over the age of 40 and more than 15% of the population over the age of 65 suffer from dry eye [<xref ref-type="bibr" rid="scirp.76229-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.76229-ref2">2</xref>] . According to a survey locally conducted, there is nearly 20% of the population with some dry eye symptoms [<xref ref-type="bibr" rid="scirp.76229-ref4">4</xref>] . The paucity of data on the epidemiology of DED in Niger Delta, Nigeria has necessitated this study in Aluu community.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>This was a cross-sectional, population-based study to determine the prevalence of Dry Eye Disease in Aluu community during a free medical out-reach expedition organized by the Salvation Ministries Port Harcourt from 16<sup>th</sup> to 18<sup>th</sup> June 2016.</p><p>Aluu is a rural community in Ikwerre Local Government Area of Rivers State, Nigeria. The community has a projected population of 12,300 people (2006 projected population) [<xref ref-type="bibr" rid="scirp.76229-ref9">9</xref>] . It is located about 20 km from the state capital-Port Harcourt and about 15 km from the local government headquarters-Isiokpo. Aluu plays host to the University of Port Harcourt. It comprises of nine villages each headed by a chief. The community has a paramount rural-Nye-we-ali Aluu, a second class chief who oversees the affairs of the entire Aluu community. It has two Primary Health Centers, one of which is affiliated to the Community Medicine Department of University of Port Harcourt Teaching Hospital. Final year medical students as well as Public/Community Health Doctors routinely undergo various outreach programmes in the primary health center. The Primary Health Center provides health care services to the entire people of Aluu and its environs.</p><p>Ethical approval for the study was obtained from the Research and Ethics Committee of the University of Port Harcourt. One thousand residents of Aluu community that participated in the free medical out-reach expedition and verbally consented to ocular examinations were recruited in the study. Consent and permission to carry out this study among the population was also obtained from the family heads/chiefs. The subjects were told that participation was absolutely voluntary and that the survey will be free of charge.</p><p>Basic eye examinations included checking the eyelids for trichiasis, globe for phthisis, cornea for opacity or pterygium and lens for obvious opacity. Special eye examination with pen torch for cornea opacities, pupil for pupillary light reaction and lens for any visible opacities. Basal and reflex tear secretion was measured by using the Schirmer test [<xref ref-type="bibr" rid="scirp.76229-ref10">10</xref>] by using 5 mm by 35 mm Whatmans filter paper without prior instillation of topical anaesthetic drops (schemer method 1). The filter paper was folded 5 mm from one end and inserted midway between the outer and middle third of the lower lid. The participants were allowed to gently close their eyes for 5 minutes after which the paper was removed and the amount of wetting measured from the fold. The measurements were done with the subjects in sitting position.</p><p>A reading of less than 10 mm was diagnostic of dry eye and graded as follows: Nomal (&gt;15 mm), Mild (9 - 14 mm) Moderate (4 - 8 mm) and Severe (&lt;4 mm) [<xref ref-type="bibr" rid="scirp.76229-ref11">11</xref>] .</p>Data Analysis<p>Data obtained was recorded on the data form for all participants and was cross checked by the principal investigator for correctness and completeness and any omission was corrected. Information from the data forms was entered into a spread sheet using statistical package for social sciences (SPSS) 16.0 for Windows statistical software and then used for statistical analysis. Frequency distribution tables or summary statistics was generated for all variables; differences were examined using Chi-square test and Student’s t-test of significance for discrete and continuous variables, respectively. 95% Confidence intervals were tabulated. The independent association of risk factors with dry eye was assessed by the multiple logistic regression analysis test. Odds ratio was used to study the strength of the association of risk factors and dry eye. An observation was considered statistically significant when p-value was less than 0.05.</p></sec><sec id="s3"><title>3. Results</title><p>A total of 730 persons (210 males and 520 females) participated in the study. This gives a male to female ratio of 1:2.5.</p><p>The modal age group was 21 - 30 years [<xref ref-type="table" rid="table1">Table 1</xref>]. The mean age was 34.2 &#177; 12.4 and age range was 8 - 64. The difference in the gender distribution in this study was statistically significant (p = 0.000) [<xref ref-type="table" rid="table1">Table 1</xref>].</p><p>Over 72% of the study population had normal Schimer’s test 95% CI [15.0 - 15.2], 18.4% had mild dry eye syndrome 95% CI [10.1 - 10.7], 6.8% had moderate dry eye syndrome test 95% CI [5.5 - 7.6] while 2.2% had severe dry eye syndrome test 95% CI [3.0 - 3.8] [<xref ref-type="table" rid="table2">Table 2</xref>].</p><p>The difference in the prevalence of DED among the various genders was statistically significant [<xref ref-type="table" rid="table3">Table 3</xref>].</p><p>The difference in the prevalence of DED among the various age groups was statistically significant [<xref ref-type="table" rid="table4">Table 4</xref>].</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Age-gender distribution of the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Age Group (Years)</th><th align="center" valign="middle"  colspan="2"  >Gender</th><th align="center" valign="middle"  rowspan="2"  >Total (%)</th></tr></thead><tr><td align="center" valign="middle" >Male (%)</td><td align="center" valign="middle" >Female (%)</td></tr><tr><td align="center" valign="middle" >&lt;20</td><td align="center" valign="middle" >40 (5.5)</td><td align="center" valign="middle" >60 (8.2)</td><td align="center" valign="middle" >100 (13.7)</td></tr><tr><td align="center" valign="middle" >21 - 30</td><td align="center" valign="middle" >10 (1.4)</td><td align="center" valign="middle" >190 (26.0)</td><td align="center" valign="middle" >200 (27.4)</td></tr><tr><td align="center" valign="middle" >31 - 40</td><td align="center" valign="middle" >50 (6.9)</td><td align="center" valign="middle" >140 (19.1)</td><td align="center" valign="middle" >190 (26.0)</td></tr><tr><td align="center" valign="middle" >41 - 50</td><td align="center" valign="middle" >70 (9.6)</td><td align="center" valign="middle" >90 (12.3)</td><td align="center" valign="middle" >160 (21.9)</td></tr><tr><td align="center" valign="middle" >51 - 60</td><td align="center" valign="middle" >30 (4.1)</td><td align="center" valign="middle" >40 (5.5)</td><td align="center" valign="middle" >70 (9.6)</td></tr><tr><td align="center" valign="middle" >61 and Above</td><td align="center" valign="middle" >10 (1.4)</td><td align="center" valign="middle" >(-)</td><td align="center" valign="middle" >10 (1.4)</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >210 (28.9)</td><td align="center" valign="middle" >520 (71.1)</td><td align="center" valign="middle" >730 (100)</td></tr><tr><td align="center" valign="middle"  colspan="4"  >Pearson Chi Square = 110.919; p = 0.000; df = 5</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution of Dry Eye Disease (DED) among the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >DED</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Percentage</th><th align="center" valign="middle" >Mean SD</th><th align="center" valign="middle" >CI</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle" >Normal (&gt;15 mm)</td><td align="center" valign="middle" >530</td><td align="center" valign="middle" >72.6</td><td align="center" valign="middle" >15.4 &#177; 0.36</td><td align="center" valign="middle" >15.0 to 15.2</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Mild (9 - 14 mm)</td><td align="center" valign="middle" >134</td><td align="center" valign="middle" >18.4</td><td align="center" valign="middle" >10.6 &#177; 0.89</td><td align="center" valign="middle" >10.1 to 10.7</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Moderate (4 - 8 mm)</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >6.8</td><td align="center" valign="middle" >5.7 &#177; 1.5</td><td align="center" valign="middle" >5.5 to 7.6</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Severe (&lt;4 mm)</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >2.2</td><td align="center" valign="middle" >3.3 &#177; 0.4</td><td align="center" valign="middle" >3.0 to 3.8</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >730</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution of DED according to gender</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  colspan="3"  >Gender</th><th align="center" valign="middle"  rowspan="2"  >Total</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >Male</td><td align="center" valign="middle" >Female</td></tr><tr><td align="center" valign="middle" >DED (Yes)</td><td align="center" valign="middle" >40</td><td align="center" valign="middle"  colspan="2"  >160</td><td align="center" valign="middle" >200</td></tr><tr><td align="center" valign="middle" >(No)</td><td align="center" valign="middle" >170</td><td align="center" valign="middle"  colspan="2"  >360</td><td align="center" valign="middle" >530</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >210</td><td align="center" valign="middle"  colspan="2"  >520</td><td align="center" valign="middle" >730</td></tr><tr><td align="center" valign="middle"  colspan="5"  >Pearson Chi Square = 10.333; p = 0.001</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Distribution of DED according to age group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle"  colspan="6"  >Age Group (Years)</th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >&lt;20</td><td align="center" valign="middle" >21 - 30</td><td align="center" valign="middle" >31 - 40</td><td align="center" valign="middle" >41 - 50</td><td align="center" valign="middle" >51 - 60</td><td align="center" valign="middle" >61 &amp; above</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >DED Yes</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >60</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >200</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >160</td><td align="center" valign="middle" >130</td><td align="center" valign="middle" >110</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >530</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >100</td><td align="center" valign="middle" >200</td><td align="center" valign="middle" >190</td><td align="center" valign="middle" >160</td><td align="center" valign="middle" >70</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >730</td></tr><tr><td align="center" valign="middle"  colspan="8"  >Pearson Chi Square = 58.493; p = 0.000; df = 5</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>The prevalence of Dry Eye Disease in this study was 27.4% [<xref ref-type="table" rid="table2">Table 2</xref>]. Prevalence of DED in different population based-studies had been reported with varying range of 5.7% to 57.5% [<xref ref-type="bibr" rid="scirp.76229-ref12">12</xref>] - [<xref ref-type="bibr" rid="scirp.76229-ref17">17</xref>] and 17.0% - 29.9% in hospital based-studies [<xref ref-type="bibr" rid="scirp.76229-ref18">18</xref>] . This variation may be due to the different geographical locations and different populations studied. More importantly, there has been lack of consistency in the diagnostic tests and definition criteria. Different authors have used different tests such as tear break-up time, corneal staining, meibomian gland digital expression, tear osmolarity, Schirmer test and assessment of the symptoms using ocular surface disease index (OSDI) [<xref ref-type="bibr" rid="scirp.76229-ref6">6</xref>] .</p><p>According to 2007 report of the international dry eye workshop (DEWS) [<xref ref-type="bibr" rid="scirp.76229-ref1">1</xref>] , no single diagnostic test performed in the field or in the clinic could reliably distinguish individuals with and without dry eye. Although a variety of diagnostic tests are commonly used in the clinic, there is no consensus on which combination of tests should be used to define DED, either in the clinic or for the purposes of a research protocol [<xref ref-type="bibr" rid="scirp.76229-ref2">2</xref>] . A major problem has been the reported lack of correlation between patients’ irritative ocular symptoms and the results of selected clinical tests for dry eye [<xref ref-type="bibr" rid="scirp.76229-ref2">2</xref>] . Much of this discrepancy can be explained by the lack of repeatability of many of the clinical tests in common use [<xref ref-type="bibr" rid="scirp.76229-ref2">2</xref>] . Other possible reasons for a lack of correlation between clinical tests and irritative symptoms could be the natural inconsistency of the disease process, the “subjective” nature of symptoms, and differences in pain thresholds and cognitive responses to questions about the ocular symptoms [<xref ref-type="bibr" rid="scirp.76229-ref2">2</xref>] .</p><p>In this study, the Schimer 1 test was utilized because of its easy applicability in an epidemiological survey, speed of use, low cost and convenience. Although the Schirmer I test does not discriminate basal from reflex tearing, thereby making it difficult to determine which parameters the test is actually measuring; it is still useful in clinical practice.</p><p>In a cluster sampled, population-based cross-sectional prevalence study on dry eye disease in 5190 adult population aged 40 - 64 years in Iran, Hashemi documented that the prevalence of dry eye was 8.7% while an abnormal Schirmer score was 17.8% [<xref ref-type="bibr" rid="scirp.76229-ref15">15</xref>] . He also observed that the prevalence of dry eye syndrome was significantly higher in women and that the condition was not significantly associated with age [<xref ref-type="bibr" rid="scirp.76229-ref15">15</xref>] . This finding collaborates our observation in this study, where the female gender had a higher prevalence of DED. However, in our study age difference was a significant epidemiological factor [<xref ref-type="table" rid="table1">Table 1</xref>]. No significance in age may be because of the narrow age range among the participants in Hashemi’s study.</p><p>In an institutional cross sectional study conducted among 96 participants of young and middle aged office workers in Japan, Uchino [<xref ref-type="bibr" rid="scirp.76229-ref19">19</xref>] observed that the prevalence of dry eye disease among computer users was 57%. Uchino used self-administered questionnaire as the instrument of study among his study participants. In a web-based screening for DED study carried out on 1689 computer users aged 20 years and above, 36.2% of participants reported 5 or more dry eye symptoms. The participants that had symptoms of dry eye were investigated with schirmer test and 32.2% of them had abnormal tear production [<xref ref-type="bibr" rid="scirp.76229-ref20">20</xref>] .</p><p>The Beijing Eye Study [<xref ref-type="bibr" rid="scirp.76229-ref16">16</xref>] which was a population-based study on prevalence of dry eye among 4439 subjects with age range of 40 years and above showed that the prevalence of dry eye was 21%.</p><p>In 2003, in the United States of America, a population-based survey on prevalence of dry eye among mid-aged and above, 39,876 women participating in the Women’s Health Study showed the prevalence of DED to be 5.7% among women less than 50 years old and 7.8% among women greater than 50 years [<xref ref-type="bibr" rid="scirp.76229-ref20">20</xref>] .</p><p>In this study, female gender and increase in age are associated with dry eye disease [<xref ref-type="table" rid="table3">Table 3</xref> and <xref ref-type="table" rid="table4">Table 4</xref>]. Maissa [<xref ref-type="bibr" rid="scirp.76229-ref21">21</xref>] documented that females tend to have a reduction in the aqueous layer of the tear film with increasing age compared to males and that female gender (particularly per- and post-menopausal ages) were risk factors for dry eyes disease [<xref ref-type="bibr" rid="scirp.76229-ref1">1</xref>] . This increase in dry eye is thought to be associated with a decrease in tear production caused by hormonal changes [<xref ref-type="bibr" rid="scirp.76229-ref6">6</xref>] . Uchino and Hashemi also documented that female gender was associated with increased risk of DED [<xref ref-type="bibr" rid="scirp.76229-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.76229-ref15">15</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>The prevalence of dry eye disease in Aluu community is high. It is therefore, advocated special eye healthcare intervention by governments and non-gov- ernmental agencies be extended to this rural Niger Delta community.</p></sec><sec id="s6"><title>Cite this paper</title><p>Onua, A.A. and Chukwuka, I.O. (2017) Prevalence of Dry Eye Disease in a Rural Niger Delta Community, Southern Nigeria. Open Journal of Ophthalmology, 7, 95-102. https://doi.org/10.4236/ojoph.2017.72014</p></sec></body><back><ref-list><title>References</title><ref id="scirp.76229-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">O’Brien, P.D. and Collum, L.M.T. (2004) Dry Eye: Diagnosis and Current Treatment Strategies. Current Allergy and Asthma Reports, 4, 314-319.  
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