Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0022568 (keratitis)
 5,133 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Ivermectin seems to be a safe and effective treatment for onchocerciasis when given in a single dose, but less is known about the effects of repeated doses. Also, there seem to be differences in its effectiveness in anterior and posterior segment ocular disease. The ocular effects of ivermectin were studied in 586 villagers who were taking part in a double-blind, placebo-controlled, randomised trial in Sierra Leone. Only those who had received four doses, with 6-month intervals, of ivermectin or placebo were eligible. The 296 ivermectin-treated subjects and the 272 who received placebo were comparable with respect to age, sex, Onchocerca infection, blindness, and visual impairment before treatment. After treatment, the ivermectin group had less anterior segment disease than the placebo group, with significantly lower prevalences of microfilariae in the anterior chamber and cornea, and punctate keratitis (all p less than 0.001), and iritis (p less than 0.05). There was no significant difference in the prevalence of sclerosing keratitis, optic atrophy, or chorioretinitis between the groups. Visual acuities tended to be better in the ivermectin group, but the difference was not significant. There was a small but significant (p less than 0.01) excess of vascular sheathing in the ivermectin group. These differences persisted when subjects who were blind or visually impaired at baseline were excluded from analysis. The long-term effects of ivermectin, particularly on posterior segment disease, need further evaluation. In the mean time, the mass distribution of ivermectin should be promoted for all communities with hyperendemic onchocerciasis at risk of anterior segment disease.
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PMID:Effects of repeated doses of ivermectin on ocular onchocerciasis: community-based trial in Sierra Leone. 168 43

Results are presented for five villages in the forest zone of Sierra Leone in which forest onchocerciasis was considered to be a significant health problem. All five villages were found to be hyperendemic and 85% (682/803) of persons were found to have at least one sign of onchocerciasis. The emergence of microfilariae from skin snips (iliac crest and/or canthus) or the presence of nodules accounted for 96.5% of all persons positive for onchocerciasis. The prevalence of nodules from all body sites was 70.5% and of elephantiasis, hanging groin and skin lesions (moderate and severe) was 0.4%, 0.3% and 5.3% respectively. Analysis of eye lesions (the most serious clinical manifestation of the disease) was restricted to persons aged 30 years and over since this gives a better indication of the public health importance of onchocerciasis than analysis in the overall population. This gave prevalence rates of onchocercal blindness of 4.5% (both eyes) and 2.8% (one eye only). Rates for the four potentially blinding eye lesions were sclerosing keratitis (4.1%), iritis (16.5%), optic atrophy (13.8%) and choroidoretinitis (14.4%). Rates in males were approximately twice as high as those in females.
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PMID:Epidemiological studies of onchocerciasis in forest villages of Sierra Leone. 319 71

The overall prevalence of onchocerciasis was 78% and 73% in three villages of the woodland savanna of Koinadugu and four villages of the savanna-forest mosaic of Kambia respectively. The total number of persons examined was 611. In Koinadugu the prevalence of microfilariae of Onchocerca volvulus in skin snips from the iliac crest and canthus was 51.3% and 22.5% respectively while corresponding figures for Kambia were 52.2% and 19.3%. The pattern of clinical manifestations were similar in both districts, the overall rates for nodules, skin lesions (moderate and severe) and leg elephantiasis being 53.2%, 12.5% and 0.3% respectively. No cases of hanging groin were seen. The prevalence of onchocercal eye lesions was lower in the present surveys than in our own findings in Guinea or the findings of other investigators in the Guinea or Sudan savanna of West Africa. In the present study prevalences of the fourmain blinding eye lesions in persons aged 30 years or more were sclerosing keratitis (3.7%), iritis (8.7%), optic atrophy (14.2%) and choroidoretinitis (11.3%), and the prevalence of blindness was 4.2% (both eyes) and 2.0% (one eye). Males were more commonly affected than females. Further entomological studies are needed to elucidate the relative role played by the different cytospecies of Simulium damnosum s.l. in the transmission of onchocerciasis in the savanna of Sierra Leone.
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PMID:Epidemiological studies of onchocerciasis in savanna villages of Sierra Leone. 319 72

Very little of the original primary forest remains in Sierra Leone and the savanna is mainly woodland or a forest-savanna mosaic. The prevalence of microfilariae of Onchocerca volvulus, nodules and moderate or severe skin lesions was higher in forest than savanna villages. In forest villages the prevalence of microfilariae was 71.8% at the iliac crest, 36.6% (outer canthus), 12.8% (cornea) and 34.1% in the anterior chamber of the eye. Corresponding figures for the savanna villages were 51.9%, 20.5%, 5.6% and 21.8%. The overall prevalence of nodules in the forest and savanna was 70.5% and 53.2% respectively, while the prevalence of head and upper body nodules was 14.8% (forest) and 11.0% (savanna). The prevalence of moderate or severe skin lesions was 17.7% in forest and 13.0% in savanna villages. Lesions of the groin and scrotum were few in both zones. In persons aged 30 years or more the prevalence rates of severe eye lesions--sclerosing keratitis, iritis, optic atrophy and choroidoretinitis--were 4.3%, 16.1%, 13.9% and 14.8% respectively in forest villages. Corresponding figures for the savanna villages were 3.7%, 8.7%, 14.2% and 11.3%. Males were more commonly affected than females. At least one of these lesions was found in 32% persons in forest and 24% in savanna villages.
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PMID:Onchocerciasis in Sierra Leone.2: A comparison of forest and savanna villages. 325 13

The relationship between severe onchocercal eye lesions (iritis, sclerosing keratitis, optic atrophy and choroidoretinitis) and (i) the prevalence and intensity of microfilariae (mf) of Onchocerca volvulus in skin snips from the iliac crest and outer canthus, and (ii) the prevalence of mf in the cornea and anterior chamber of the eye, was studied in 1414 persons from forest and savanna villages and 312 attenders at eye clinics. Ecologically the savanna of Sierra Leone more closely resembles the forest than the dry Sudan-savanna areas of West Africa, and in persons aged 30 years or more the combined prevalence of anterior segment lesions (iritis and sclerosing keratitis) was higher in the forest villages (20.6%) than in the savanna (12.7%). The higher loads of mf found in the forest compared to savanna villages could explain these results. Prevalence rates for posterior segment lesions (optic atrophy and choroidoretinitis) were 28.1% and 22.6% in the forest and savanna respectively. Although in villages from both zones there was a close association between mf in the anterior chamber and optic atrophy, other associations between posterior segment lesions and mf were either not significant or weak. In contrast, there was a strong association between anterior segment lesions and mf in the eye and the concentration of mf at the outer canthus. This association was stronger for iritis than for sclerosing keratitis.
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PMID:Onchocerciasis in Sierra Leone 3: Relationships between eye lesions and microfilarial prevalence and intensity. 325 14

Thirty consecutive patients with biopsy-proved mycosis fungoides were examined ophthalmologically. Specific ocular changes, judged directly related to the mycosis fungoides, were found in 11 of the 30 subjects, usually in the late plaque or tumor stages of the disease. Tumors, especially involving the lids, were the most common ophthalmic finding. Keratitis, uveitis, and optic atrophy were also described. A review of the literature is given, and changes found in patients in this series correlate well with ophthalmic findings presented in diverse isolated case reports. It seems that the frequency of ophthalmic pathologic findings in mycosis fungoides is much more common than previously assumed.
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PMID:Ocular findings in mycosis fungoides. 746 64

Little is known of the epidemiology and clinical picture of ocular onchocerciasis in South America. A survey of onchocercal eye disease was performed in the hyperendemic area of a rain forest focus of onchocerciasis in Esmeraldas Province in Ecuador. A total of 785 skin snip positive individuals from black and Chachi Amerindian communities were examined. The blindness rate attributable to onchocerciasis was 0.4%, and 8.2% were visually impaired. Onchocercal ocular lesions were seen in a high proportion of the study group: 33.6% had punctate keratitis, microfilariae in the anterior chamber and cornea were seen in 28.9% and 33.5% respectively, iridocyclitis was seen in 1.5%, optic atrophy in 5.1%, and chorioretinopathy in 28.0%. Sclerosing keratitis was not seen. The prevalence of all ocular lesions increased with age. Punctate keratitis was strongly associated with microfilarial counts in the cornea and chorioretinopathy was correlated with infection intensities in the cornea and anterior chamber. Chachi Amerindians had higher anterior chamber microfilarial counts and a greater prevalence of punctate keratitis than blacks though blacks had a greater prevalence of iridocyclitis and optic nerve disease. The pattern of ocular disease resembled rain forest onchocerciasis in west Africa with few severe ocular lesions in the anterior segment and all blinding lesions attributable to posterior segment disease.
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PMID:Onchocerciasis in Ecuador: ocular findings in Onchocerca volvulus infected individuals. 769 37

Although ocular manifestations of Lyme disease have long been noted, they remain a rare feature of the disease. The spirochete invades the eye early and remains dormant, accounting for both early and late ocular manifestations. A nonspecific follicular conjunctivitis occurs in approximately 10% of patients with early Lyme disease. Keratitis occurs often within a few months of onset of disease and is characterized by nummular nonstaining opacities. Inflammatory syndromes, such as vitritis and uveitis, have been reported; in some cases, a vitreous tap is required for diagnosis. Neuro-ophthalmic manifestations include neuroretinitis, involvement of multiple cranial nerves, optic atrophy, and disc edema. Seventh nerve paresis can lead to neurotrophic keratitis. In endemic areas, Lyme disease may be responsible for approximately 25% of new-onset Bell's palsy. Criteria for establishing that eye findings can be attributed to Lyme disease include the lack of evidence of other disease, other clinical findings consistent with Lyme disease, occurrence in patients living in an endemic area, positive serology, and, in most cases, response to treatment. Management of ocular manifestations often requires intravenous therapy.
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PMID:Ocular manifestations of Lyme disease. 772 93

Crouzon's syndrome is an autosomal dominant disorder characterized by premature craniosynostosis leading to multiple ocular abnormalities and vision loss. Strabismus, optic atrophy, exposure keratitis, hypertelorism, nystagmus, and unexplained visual loss have been reported. Keratoconus has been described only once previously in a patient with other ocular abnormalities. This article reports bilateral keratoconus in a patient with Crouzon's syndrome without other ocular pathology. We emphasize the importance of early recognition and therapy of this treatable cause of decreased vision in Crouzon's syndrome.
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PMID:Bilateral keratoconus in Crouzon's syndrome. 813 12

CD4(+), CD8(+), immunoglobulin status and ocular lesions of some onchocerciasis-infected rural Nigerians as manifested by the presence of microfilariae in their skin snips and some chronic symptoms of the parasitic infestation were evaluated. The highest mean CD4(+) and mean microfilarial (mff) load of 560 +/- 20.46 unit cells/microl and 20 mff/mg were recorded among the individuals within the second decade of life, while the least mean CD4+ and mff load of 307.20 +/- 11.23 unit cell/microl and 6.5 mff/mg occurred among volunteers after 60 years of age. The highest mean CD8(+) of 388.00 +/- 23.71 unit cells/microl occurred at the third decade of life. The individuals above 60 years had the least mean CD8(+) of 350.25 +/- 11.90 unit cells/microl. The volunteers had mean CD4(+) of 372.45 +/- 109.02 unit cells/microl and mean CD8(+) of 359.42 +/- with an overall CD4(+):CD8(+) ratio of 1.04. The mean CD4(+) and mean CD8(+) had positive correlation with the mean microfilarial load (r = 0.52 and r = 0.40), respectively. The mean IgE, IgG, lgA, IgM, and IgD were 2,074.82 +/- 823.09, 19.36 +/- 2.49, 3.88 +/- 0.26, 3.59 +/- 0.38, and 0.29 +/- 0.19 mg/dl, and these immunoglobulins negatively correlated with the mean microfilarial load at r = -0.02, r = -0.15, r = -0.82, r = -0.37, and r = 0.26, respectively. Among these immunoglobulins evaluated, only mean IgE (2,074.82 +/- 823 ng/ml) was statistically different from the control subjects (0 mg/dl) at t = 3.39, P < 0.05. In all, the prevalence of the visual impairment and lesions were low. Among the six visual lesions, namely, cataract, choroidoretinitis, iridocyclitis, glaucoma, sclerosing keratitis, and optic atrophy encountered in Egoro-Eguare, only optic atrophy and sclerosing keratitis was reported among the children. The female adults had the highest prevalence of reduced vision 20(43.5%). Also, the prevalence of choroidoretinitis (2.2%) and iridocyclitis (2.2%) were the least prevalent ocular lesions reported among these female adults. The depletion of the CD4(+) contributed to the low prevalence of visual impairment and lesions in this locality. The depleted CD4(+), CD8(+), and the lower values of IgA, IgM, and IgG contributed in the maintenance of chronicity of onchocerciasis in Egoro-Eguare, Nigeria.
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PMID:CD4(+), CD8(+), immunoglobulin status and ocular lesions among some onchocerciasis-infected rural Nigerians. 1720 2


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