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1.
Zhen Ci Yan Jiu ; 46(10): 863-8, 2021 Oct 25.
Article in Chinese | MEDLINE | ID: mdl-34698461

ABSTRACT

OBJECTIVE: To observe the effect of Lingnan fire needling combined with artificial tears in the treatment of xerophthalmia. METHODS: A total of 86 xerophthalmia patients were equally and randomly divided into treatment group and control group. The patients of both groups were received treatment with 0.1% sodium hyaluronate eye drops in their eyes 3 times a day, one drop in each eye. In addition, the patients of treatment group also treated by Lingnan fire needling on bilateral Shaoze (SI1), Neichengqi and beside lacrimal puncta once a week. The treatment was conducted for 4 consecutive weeks. Before and after 4 weeks of treatment, the clinical efficacy, visual acuity, intraocular pressure, ocular symptom score, OSDI score, fluorescence staining (FL) score, schemer I, tear menisci height, tear film break-up time (BUT) and eye redness index were recorded and evaluated. RESULTS: After the treatment, self-comparison showed that the symptom score, OSDI score, FL score and eye redness index were significantly decreased (P<0.05), and BUT was notably increased in both groups (P<0.05) in comparison with their own pre-treatment. The tear menisci height in the treatment group was higher than that before the treatment (P<0.05). Comparison between the two groups showed that the symptom score, OSDI score and eye redness index were obviously lower in the treatment group than in the control group (P<0.05), whereas the BUT and tear menisci height were evidently higher (P<0.05). The total effective rate of the treatment group was 84.88% (73/86), better than 76.74% (66/86) of the control group (P<0.05). CONCLUSION: Lingnan fire needling combined with 0.1% sodium hyaluronate eye drops is more effective than simple sodium hyaluronate eye drops for xerophthalmia patients, with significant curative effect and no adverse reactions.


Subject(s)
Dry Needling , Hyaluronic Acid/therapeutic use , Ophthalmic Solutions/therapeutic use , Xerophthalmia , Humans , Tears , Xerophthalmia/drug therapy
2.
Molecules ; 23(10)2018 Oct 11.
Article in English | MEDLINE | ID: mdl-30314275

ABSTRACT

Dry eye disease is affected by a broad range of causes such as age, lifestyle, environment, medication and autoimmune diseases. These causes induce tear instability that activates immune cells and promotes expression of inflammatory molecules. In this study, we investigated the therapeutic effects of an ethanolic extract of Aucuba japonica (AJE) and its bioactive compound, aucubin, on dry eye disease. The human corneal cells were exposed to desiccation stress induced by exposing cells to air, so that viability was decreased. On the other hand, pre-treatment of AJE and aucubin restored cell survival rate depending on the dose under the dry condition. This result was confirmed again by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining. The mRNA expression of inflammatory molecules was reduced by the pretreatment of AJE and aucubin under the dry state. The therapeutic effects of AJE and aucubin were examined in the animal model for dry eye induced by unilateral excision of the exorbital lacrimal gland. Declined tear volumes and corneal irregularity in the dry eye group were fully recovered by the administration of AJE and aucubin. The apoptotic cells on the cornea were also decreased by AJE and aucubin. Therefore, this study suggests that administration of AJE can be a novel therapeutic for dry eye disease and that the pharmacological activities of AJE may be in part due to its bioactive compound, aucubin.


Subject(s)
Epithelium, Corneal/injuries , Epithelium, Corneal/metabolism , Iridoid Glucosides/pharmacology , Magnoliopsida/chemistry , Plant Extracts/pharmacology , Tears , Xerophthalmia/metabolism , Animals , Apoptosis/drug effects , Cell Survival/drug effects , Chromatography, High Pressure Liquid , Cytokines/genetics , Cytokines/metabolism , Desiccation , Disease Models, Animal , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Epithelium, Corneal/drug effects , Epithelium, Corneal/pathology , Gene Expression , Inflammation Mediators/metabolism , Iridoid Glucosides/analysis , Iridoid Glucosides/chemistry , Mice , Molecular Structure , Plant Extracts/analysis , Plant Extracts/chemistry , Protective Agents/pharmacology , Rats , Xerophthalmia/drug therapy , Xerophthalmia/etiology
3.
Nutrients ; 8(11)2016 Nov 23.
Article in English | MEDLINE | ID: mdl-27886047

ABSTRACT

The purpose of this study was to investigate the therapeutic effects of topical application of apricot kernel extract (AKE) in a unilateral exorbital lacrimal gland excision mouse model of experimental dry eye. Dry eye was induced by surgical removal of the lacrimal gland. Eye drops containing 0.5 or 1 mg/mL AKE were administered twice a day from day 3 to day 7 after surgery. Tear fluid volume and corneal irregularity scores were determined. In addition, we examined the immunohistochemical expression level of Muc4. The topical administration of AKE dose-dependently improved all clinical dry eye symptoms by promoting the secretion of tear fluid and mucin. Thus, the results of this study indicate that AKE may be an efficacious topical agent for treating dry eye disease.


Subject(s)
Cornea/drug effects , Lacrimal Apparatus/surgery , Plant Extracts/pharmacology , Prunus armeniaca/chemistry , Seeds/chemistry , Tears/metabolism , Xerophthalmia/drug therapy , Administration, Ophthalmic , Animals , Cornea/metabolism , Cornea/pathology , Cornea/physiopathology , Disease Models, Animal , Dose-Response Relationship, Drug , Female , Mice, Inbred C57BL , Mucin-4/metabolism , Ophthalmic Solutions , Phytotherapy , Plant Extracts/administration & dosage , Plant Extracts/isolation & purification , Plants, Medicinal , Time Factors , Tumor Necrosis Factor-alpha/metabolism , Xerophthalmia/metabolism , Xerophthalmia/pathology , Xerophthalmia/physiopathology
4.
Genet Mol Res ; 15(4)2016 Nov 03.
Article in English | MEDLINE | ID: mdl-27820648

ABSTRACT

Diabetes-induced xerophthalmia is a general metabolic disorder with high incidence and increased treatment difficulty. Our study aimed to explore the combined effect of traditional Chinese and Western medicines on diabetes-associated xerophthalmia. We recruited 60 diabetic xerophthalmia patients, and randomly assigned them to either the control (Western medicine treatment) or the experimental (combined treatment of traditional Chinese medicine and Western medicine) groups. Pre-treatment and post-treatment analyses were performed to assess the combined therapeutic effect of traditional Chinese and Western medicine on xerophthalmia-associated indicators. We found that the experimental group expressed reduced levels of IL-1, IL-8, and TNF-α (P < 0.05) as compared to the control group. Furthermore, the experimental group showed higher treatment efficacy as compared to the control group (85.00 vs 51.67% Z = 22.244, P < 0.05). In addition, break-up time (t = 20.582, P < 0.05) and tear section (t = 23.082, P < 0.05) was increased in the experimental group as compared to the controls. Lastly, it was found that the combined treatment of traditional Chinese and Western medicine effectively reduced corneal injuries, as indicated by reduced fluorescein staining. This study suggested that a combination treatment consisting of both traditional Chinese and Western medicines may be effective against xerophthalmia in diabetes, and that inflammatory factors are potential biomarkers to examine the treatment efficacy.


Subject(s)
Diabetes Mellitus/pathology , Drugs, Chinese Herbal/therapeutic use , Inflammation Mediators/metabolism , Medicine, Chinese Traditional , Xerophthalmia/drug therapy , Xerophthalmia/etiology , Adolescent , Adult , Aged , Case-Control Studies , Diabetes Mellitus/drug therapy , Drug Therapy, Combination , Humans , Middle Aged , Tears/metabolism , Treatment Outcome , Young Adult
5.
Oxid Med Cell Longev ; 2016: 4727415, 2016.
Article in English | MEDLINE | ID: mdl-27313829

ABSTRACT

Purpose. To investigate the therapeutic effects of topical administration of antioxidant medicinal plant extracts in a mouse model of experimental dry eye (EDE). Methods. Eye drops containing balanced salt solution (BSS) or 0.001%, 0.01%, and 0.1% extracts were applied for the treatment of EDE. Tear volume, tear film break-up time (BUT), and corneal fluorescein staining scores were measured 10 days after desiccating stress. In addition, we evaluated the levels of interleukin- (IL-) 1ß, tumor necrosis factor- (TNF-) α, IL-6, interferon- (IFN-) γ, and IFN-γ associated chemokines, percentage of CD4+C-X-C chemokine receptor type 3 positive (CXCR3+) T cells, goblet cell density, number of 4-hydroxy-2-nonenal (4-HNE) positive cells, and extracellular reactive oxygen species (ROS) production. Results. Compared to the EDE and BSS control groups, the mice treated with topical application of the 0.1% extract showed significant improvements in all clinical parameters, IL-1ß, IL-6, TNF-α, and IFN-γ levels, percentage of CD4+CXCR3+ T cells, goblet cell density, number of 4-HNE-positive cells, and extracellular ROS production (P < 0.05). Conclusions. Topical application of 0.1% medicinal plant extracts improved clinical signs, decreased inflammation, and ameliorated oxidative stress marker and ROS production on the ocular surface of the EDE model mice.


Subject(s)
Anti-Inflammatory Agents/administration & dosage , Antioxidants/administration & dosage , Eye/drug effects , Oxidative Stress/drug effects , Plant Extracts/administration & dosage , Tears/drug effects , Xerophthalmia/drug therapy , Administration, Ophthalmic , Aldehydes/metabolism , Animals , Cytokines/metabolism , Disease Models, Animal , Dose-Response Relationship, Drug , Eye/metabolism , Eye/physiopathology , Female , Goblet Cells/drug effects , Goblet Cells/metabolism , Inflammation Mediators/metabolism , Mice, Inbred C57BL , Ophthalmic Solutions , Phytotherapy , Plants, Medicinal , Reactive Oxygen Species/metabolism , Tears/metabolism , Time Factors , Xerophthalmia/metabolism , Xerophthalmia/physiopathology
6.
Zhongguo Zhong Yao Za Zhi ; 40(6): 1151-5, 2015 Mar.
Article in Chinese | MEDLINE | ID: mdl-26226762

ABSTRACT

OBJECTIVE: To investigate the efficiency of Spanishneedles Herb eye drops in treating perimenopausal xerophthalmia in rabbits. METHOD: Totally 36 rabbits (36 right eyes) were ovariectomized, and 2 months later divided into three groups: the experimental group (group A, n = 12) given Spanishneedles Herb eye drops, the control group (group B, n = 12) given PBS and the model group (group C, n = 12) given no drug. The Schirmer I test (SIT), fluorescent (FL), total tear protein, diastase activity, lactoferrin and lysozyme contents and confocal scanning microscopy were performed at before the treatment and at 1 w, 2 w, 1 mo, 2 mo after the treatment. RESULT: Before the treatment, There was no significant difference in SIT, FL, total tear protein, lysozyme, lactoferrin and amylase activity between two groups. Two months later after the treatment, both the group B and the group A showed differences degrees of changes in SIT, FL, total tear protein, lysozyme, lactoferrin and amylase activity compared with that before the treatment, with statistical differences (P < 0.05); At each time point, both groups revealed statistical differences in SIT, FL, total tear protein, lysozyme, lactoferrin and amylase activity (1 < 0.05). Two months later alter the treatment, densities of basal epithelial cells and inflammatory cells in the group A were (4 122 ±416) cells/mm2 and (339 ± 131) cells/mm2, while that in the group B were (3 343 ± 424) cells/mm2 and (49 ± 17) cells/mm2, with statistical differences between them (P < 0.05). CONCLUSION: Spanishneedles Herb eye drops could effectively treat perimenopausal xerophthalmia in rabbit caused by sex hormones decline.


Subject(s)
Asteraceae/chemistry , Drugs, Chinese Herbal/administration & dosage , Ophthalmic Solutions/administration & dosage , Xerophthalmia/drug therapy , Animals , Female , Humans , Perimenopause/drug effects , Perimenopause/metabolism , Rabbits , Tears/metabolism , Xerophthalmia/metabolism
7.
Zhongguo Zhen Jiu ; 34(10): 1005-8, 2014 Oct.
Article in Chinese | MEDLINE | ID: mdl-25543437

ABSTRACT

Professor ZHOU Yun-xian's clinical experience of acupuncture combined with Chinese material medica for xerophthalmia is introduced. Her treatment for xerophthalmia is firstly focused on syndrome differentiation, indicating that different syndrome has different treatment of acupuncture and Chinese material medica. It is emphasized that by following the holistic concept of TCM, the local acupoints and whole-body acupoints cooperate closely, forming her special combination method of acupoints. In clinic, attention is focused on the application of many acupuncture techniques and extra points. With the combination of acupuncture and Chinese material medica, the treatment is flexible with superior clinical efficacy.


Subject(s)
Acupuncture Therapy , Drugs, Chinese Herbal/therapeutic use , Xerophthalmia/therapy , Combined Modality Therapy , Female , Humans , Male , Middle Aged , Xerophthalmia/drug therapy
8.
Panminerva Med ; 56(3 Suppl 1): 1-6, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25208615

ABSTRACT

AIM: Dry eye symptoms, resulting from insufficient tear fluid generation, represent a considerable burden for a largely underestimated number of people. We concluded from earlier pre-clinical investigations that the etiology of dry eyes encompasses oxidative stress burden to lachrymal glands and that antioxidant MaquiBright™ Aristotelia chilensis berry extract helps restore glandular activity. METHODS: In this pilot trial we investigated 13 healthy volunteers with moderately dry eyes using Schirmer test, as well as a questionnaire which allows for estimating the impact of dry eyes on daily routines. Study participants were assigned to one of two groups, receiving MaquiBright™ at daily dosage of either 30 mg (N.=7) or 60 mg (N.=6) over a period of 60 days. Both groups presented with significantly (P<0.05) improved tear fluid volume already after 30 days treatment. Schirmer test showed an increase from baseline 16.3±2.6 mm to 24.4±4.8 mm (P<0.05) with 30 mg MaquiBright™ and from 18.7±1.9 mm to 27.6±3.4 mm with 60 mg (P<0.05), respectively. Following treatment with 30 mg MaquiBright™ for further 30 days, tear fluid volume dropped slightly to 20.5±2.8 mm, whereas the improvement persisted with 60 mg treatment at 27.1±2.7 mm after 60 days treatment (P<0.05 vs. baseline). RESULTS: The burden of eye dryness on daily routines was evaluated employing the "Dry Eye-related Quality of life Score" (DEQS), with values spanning from zero (impact) to a maximum score of 60. Participants had comparable baseline values of 41.0±7.7 (30 mg) and 40.2±6.3 (60 mg). With 30 mg treatment the score significantly decreased to 21.8±3.9 and 18.9±3.9, after 30 and 60 days, respectively. With 60 mg treatment the DEQS significantly decreased to 26.9±5.3 and 11.1±2.7, after 30 and 60 days, respectively. Blood was drawn for safety analyses (complete blood rheology and -chemistry) at all three investigative time points without negative findings. CONCLUSION: In conclusion, while daily supplementation with 30 mg MaquiBright™ is effective, the dosage of 60 significantly increased tear fluid volume at all investigative time points and decreased dry eye symptoms to almost a quarter from initial values after two months treatment.


Subject(s)
Elaeocarpaceae , Lacrimal Apparatus/drug effects , Plant Extracts/therapeutic use , Tears/metabolism , Xerophthalmia/drug therapy , Adult , Dose-Response Relationship, Drug , Elaeocarpaceae/chemistry , Female , Fruit , Humans , Lacrimal Apparatus/metabolism , Male , Phytotherapy , Pilot Projects , Plant Extracts/isolation & purification , Plants, Medicinal , Recovery of Function , Surveys and Questionnaires , Time Factors , Treatment Outcome , Xerophthalmia/diagnosis , Xerophthalmia/physiopathology
9.
Can J Ophthalmol ; 49(1): 109-12, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24513368

ABSTRACT

OBJECTIVE: To report the ocular features, underlying systemic conditions, and management of diet-induced vitamin A deficiency in Scottish adults. DESIGN: Retrospective case series. METHODS: Three middle-aged white adults presented with ocular signs of xerophthalmia and keratomalacia that led to the diagnosis of previously undiagnosed vitamin A deficiency. Case 1 presented with rapidly progressing bilateral keratomalacia with corneal perforation, whereas Cases 2 and 3 presented with conjunctival and corneal xerosis. RESULTS: Corneal gluing was performed in Case 1. Cases 2 and 3 were treated topically with preservative-free tears, retinoic acid, and punctual plugs to optimize the ocular surface. This, combined with dietary supplementation, resulted in normalizing the ocular surface. CONCLUSIONS: Diet-induced vitamin A deficiency can occur in middle-aged white adults. Ocular surface changes may be the presenting sign of hypovitaminosis A in the Western world. A high degree of suspicion with prompt recognition and management of the underlying dietary deficiency can lead to complete reversal of the ocular surface changes.


Subject(s)
Diet , Vitamin A Deficiency/complications , Xerophthalmia/etiology , Adult , Female , Humans , Male , Middle Aged , Retrospective Studies , Vitamin A/therapeutic use , Vitamin A Deficiency/diagnosis , Vitamin A Deficiency/drug therapy , Vitamin A Deficiency/etiology , Vitamins/therapeutic use , Xerophthalmia/diagnosis , Xerophthalmia/drug therapy
10.
Eye (Lond) ; 28(5): 621-3, 2014 May.
Article in English | MEDLINE | ID: mdl-24525868

ABSTRACT

PURPOSE: Xerophthalmia refers to the ocular manifestations associated with vitamin A deficiency, including xerosis, keratomalacia, nyctalopia and Bitot's spot. Hypovitaminosis A is well-recognised in developing countries, but is rare in the developed world. Most cases in the latter relate to fat malabsorption. Conditions in which vitamin A metabolism or storage is deranged (chronic liver disease, including alcoholism) are also aetiologies. We wanted to see whether this was common in our department. METHODS: Oral vitamin A supplements were given to patients who presented with hypovitaminosis A. RESULTS: All patients were found to have hypovitaminosis A on biochemical testing and responded dramatically to oral vitamin A supplementation, resulting in an improved final visual outcome. DISCUSSION: This series demonstrates that prompt recognition and treatment of xerophthalmia can lead to rapid recovery and avert significant visual morbidity. The prevalence of xerophthalmia is likely to increase in the developed world largely owing to alcoholic liver disease. It is thought by some that we are on the verge of a potential epidemic. We hope that by increasing the profile of this important public health issue, we may be able to influence future prevalence of hypovitaminosis.


Subject(s)
Vitamin A Deficiency/complications , Xerophthalmia/etiology , Adult , Female , Humans , Male , Middle Aged , Treatment Outcome , Vitamin A/therapeutic use , Vitamin A Deficiency/diagnosis , Vitamin A Deficiency/drug therapy , Vitamins/therapeutic use , Xerophthalmia/drug therapy
11.
Rev. Asoc. Esp. Espec. Med. Trab ; 22(3): 120-129, sept. 2013.
Article in Spanish | IBECS | ID: ibc-116156

ABSTRACT

Existe relación entre trabajadores expuestos a pantallas de visualización de datos y alteraciones de la superficie ocular, medida por citoquinas/quimioquinas que pueden mejorar con la suplementación de ácidos omega-3 y medidas de promoción de la salud en el lugar de trabajo. La prolongación de la vida laboral y el alto nivel de exposición obligan a intervenir a los Servicios de Prevención de Riesgos Laborales (AU)


There is relationship between workers exposed to data visualization screens and ocular surface alterations, measured by cytokines/chemokines that may benefit from supplementation of omega-3 and measures of health promotion in the workplace. The extension of working life and require high level of exposure to intervene Services Occupational Risk Prevention (AU)


Subject(s)
Humans , Xerophthalmia/drug therapy , Occupational Diseases/prevention & control , Cathode Ray Tube/adverse effects , Occupational Risks , Occupational Exposure/adverse effects , Fatty Acids, Omega-3/therapeutic use , Cytokines/analysis , Chemokines/therapeutic use , Inflammation Mediators/analysis
12.
Zhongguo Zhong Yao Za Zhi ; 37(19): 2985-9, 2012 Oct.
Article in Chinese | MEDLINE | ID: mdl-23270247

ABSTRACT

OBJECTIVE: To investigate the clinical effect of spanishneedles leaves on middle and severe xerophthalmia of menopausal females. METHOD: This study was a prospective random controlled trial. Ninty-six menopausal females diagnosed with xerophthalmnia (aged from 40 to 50) were randomly divided into in two groups: group A' the spanishneedles leaves group (n=48) and group B' the control group (n=48). Both groups were treated with Forte eye drops. All patients were detected at 3, 7, 28 h before and after treatment to evaluate subjective symptoms, OSDI and four tear film indicators. Variance analysis and differential analysis on sample average or median were made on both groups before and after treatment. RESULT: There were no significant difference in symptom and diction indicators between both groups before treatment. For 28 d after treatment, among middle and severe xerophthalmia samples of the spanishneedles leaves group, the mean differences showed significant improvement compared with that before treatment , OSDI and four tear film indicators also showed improvement to varying degrees. For 28 d after treatment, among middle and severe xerophthalmia samples of the vitamin C group, the mean differences showed no significant improvement compared with that before treatment , OSDI and four tear film indicators also showed no remarkable improvement. There were significant differences in OSDI, BUT, SIT, height of tear meniscus and FL between both groups. CONCLUSION: Spanishneedles leaves can effectively improve symposiums and signs of middle and severe xerophthalmia among menopausal females and thus showing clinical significance to some extent.


Subject(s)
Menopause , Plant Leaves/chemistry , Plants, Medicinal , Xerophthalmia/drug therapy , Adult , Female , Humans , Middle Aged , Treatment Outcome
14.
JPEN J Parenter Enteral Nutr ; 36(3): 361-4, 2012 May.
Article in English | MEDLINE | ID: mdl-22269897

ABSTRACT

Biliopancreatic diversion is a predominantly malabsorptive bariatric procedure that can lead to the development of several nutrition complications, including fat-soluble vitamin deficiencies. Routine supplementation with vitamins and trace elements and a strict medical follow-up are essential to prevent these nutrition risks. Vitamin A deficiency is common after bariatric surgery but rarely causes clinical symptoms. Case reports have described ophthalmological and fetal complications associated with vitamin A deficiency after malabsorptive bariatric surgery. Phrynoderma is a type of follicular hyperkeratosis located on the extensor surfaces of the extremities whose main cause is vitamin A deficiency. The simultaneous occurrence of phrynoderma and ocular symptoms secondary to hypovitaminosis A after bariatric surgery is exceptional. The authors describe a man who presented follicular hyperkeratosis with nyctalopia and xerophthalmia that had appeared 1 year after biliopancreatic diversion. He admitted poor compliance with diet and daily supplementation of vitamins and oligoelements. Serum vitamin A levels were decreased. Treatment with high doses of vitamin A was associated with a clear improvement of cutaneous and ocular lesions with complete resolution after 2 months. The patient was readmitted 2 years later because of the reappearance of cutaneous lesions and micronutrient deficiency. Revisional bariatric surgery was performed. The authors review and discuss the relationship between phrynoderma, malnutrition, and vitamin A deficiency.


Subject(s)
Biliopancreatic Diversion/adverse effects , Keratosis/etiology , Vitamin A Deficiency/complications , Vitamin A Deficiency/diagnosis , Diet , Dietary Supplements , Humans , Keratosis/drug therapy , Keratosis/pathology , Male , Middle Aged , Night Blindness/drug therapy , Night Blindness/etiology , Obesity, Morbid/surgery , Postoperative Complications , Vitamin A/administration & dosage , Vitamin A/blood , Vitamin A Deficiency/drug therapy , Xerophthalmia/drug therapy , Xerophthalmia/etiology
15.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 29(7): 646-9, 2009 Jul.
Article in Chinese | MEDLINE | ID: mdl-19852302

ABSTRACT

OBJECTIVE: To objectively evaluate the therapeutic effect and safety of Runmushu Oral Liquid (RMS) for the treatment of xerophthalmia in postmenopausal women. METHODS: Seventy-two postmenopausal women (144 eyes) with xerophthalmia of aqueous tear deficiency type were assigned to two groups. Patients in the treated group were treated with RMS (consisted of prepared and crude rehmannia root, figwort, lilyturf root, dendrobium stem, wolfberry fruit, chrysanthemum and sticktight) orally combining with local applying of Hialid eye drops; while those in the control group were treated with Hialid eye drops alone. Changes of subjective symptoms and objective indices in the two groups were observed and compared before and after 1-month treatment. RESULTS: After 1 month of treatment, the total effective rate was 86.1% (62/72) in the treated group and 66.7% (48/72) in the control group, showing significant difference between them (P < 0.01). Significant differences between groups were also shown in improvements of total scores of subjective symptoms (P < 0.01), scores of tear film break-up time (BUT) and Schirmer I test, these indices in the treated group were better (P < 0.01). However, the improvement of cornea fluorescin staining scores was insignificant different between groups (P > 0.05). CONCLUSION: RMS with artificial-tears can alleviate the eye symptoms, prolong the BUT, promote the secretion of tears in treating postmenopausal women xerophthalmia, showing a therapeutic effect superior to that by artificial-tears alone.


Subject(s)
Drugs, Chinese Herbal/therapeutic use , Phytotherapy , Xerophthalmia/drug therapy , Aged , Female , Humans , Middle Aged , Ophthalmic Solutions/therapeutic use , Postmenopause , Treatment Outcome
16.
Ophthalmic Physiol Opt ; 29(6): 573-83, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19686307

ABSTRACT

PURPOSE: To objectively review the outcome of clinical studies where rose bengal stain (RB) has been used as an outcome measure to assess the efficacy of artificial tears (AT) in patients with dry eye. METHODS: From peer-reviewed articles published between 1947 and 2008, information was sought on dry eye status, as reported using a grading scheme, after use of RB as a diagnostic test, before and after use of a specific regimen of artificial tears or ocular lubricants for approximately 30 days. Mean baseline scores and post-treatment scores were calculated, along with the net change and the percentage change in the RB scores. RESULTS: From a total of 33 suitable data sets, published between 1985 and 2006, the group mean pre-treatment RB score was 4.25 +/- 1.55 (+/-S.D.), which decreased to 2.84 +/- 1.24 after 30 days of treatment. This represented a net change of -1.43 (95% CI of -1.04 to -1.45). For use of traditional AT (saline, hypromellose, etc), the net change was -0.95, it was -1.33 for use of carbomer (polyacrylic acid) gels and -2.10 for hyaluronic acid (HA) products. These changes represented net improvements of 25.9 +/- 18.4%, 38.0 +/- 20.7% and 41.8 +/- 16.3% respectively. The greater change with HA was not associated with a lower final outcome score, but with higher pre-treatment scores. CONCLUSIONS: Based on RB grading schemes used by numerous different clinicians over many years, treatment of dry eye with artificial tears or ocular lubricants can be expected to improve the condition of the exposed ocular surface. Assuming no improvement without treatment, a 30 days treatment period can be projected to produce an overall improvement of around 25%, but with no unambiguous statistical differences between product types.


Subject(s)
Fluorescent Dyes , Lubricants/therapeutic use , Ophthalmic Solutions/therapeutic use , Rose Bengal , Xerophthalmia/drug therapy , Adult , Aged , Female , Humans , Middle Aged , Predictive Value of Tests , Treatment Outcome
17.
Zhonghua Yan Ke Za Zhi ; 44(11): 1011-9, 2008 Nov.
Article in Chinese | MEDLINE | ID: mdl-19176098

ABSTRACT

OBJECTIVE: To assess the preventive effects of extract of Buddleja officinalis on dry eye in castrated rabbits and to discuss the mechanism of these effects. METHODS: It was a experimental study. Thirty male rabbits were divided equally into normal group (A), disease group (B) and treatment group (C, D, and E). The dry eye model was established with orchiectomy (ORX) in Group B, C, D and E. Group C, D and E were gastrically perfused with single-dose or double-does of Buddleja officinalis extract or genistein for 30 days. All rabbits were examined with Schirmer I test (SIT). TGF-beta1, IL-1beta, TNF-alpha, Fas, FasL, Bax and bcl-2 were detected by immunohistochemistry. Morphological and ultrastructure changes were observed by electron microscopy. RESULTS: The SIT value of group C, D, E was significantly greater than that of group B (P < 0.01). The expression of IL-1beta, TNF-alpha, Fas, FasL and Bax in acinar cells and glandular tube cells of group C, D, E were significantly lower than those of group B (P < 0.01) and the expression of TGF-beta1 and bcl-2 in acinar cells and glandular tube cells of group C, D, E were significantly higher than those of group B (P < 0.01). Furthermore, ultrastructure of lacrimal gland in group C, D, E was much healthier than that of group B. The results obtained from all of these studies showed that the lacrimal glands status in group C, D was significantly better than that of group E (P < 0.05). CONCLUSION: Extract of Buddleja officinalis has a significant effect on the prevention of experimental dry eye in castrated male rabbits. The main components of extract of Buddleja officinalis are the flavonoids. The flavonoids display androgen-like activity. Therefore, it can adjust gonadal hormone level in vivo. As a result, it can inhibit local inflammation in lacrimal gland and reduce apoptosis of lacrimal gland cells.


Subject(s)
Buddleja/chemistry , Flavones/therapeutic use , Phytotherapy , Plant Extracts/therapeutic use , Xerophthalmia/drug therapy , Animals , Lacrimal Apparatus/drug effects , Male , Rabbits , Xerophthalmia/prevention & control
18.
Eur J Pediatr ; 164(4): 202-6, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15789254

ABSTRACT

UNLABELLED: Cystic fibrosis (CF) is an autosomal recessive disease characterised by increased viscosity of mucus secretions and high chloride concentration in exocrine secretions. Clinically, the patients suffer from chronic pulmonary changes, chronic pancreatic deficiency, and an obstruction of the gastrointestinal tract. The disease affects all secretory epithelia including the eye. The influence of nutritional status on long-term survival and quality of life of CF patients is well documented. Steatorrhea, a consequence of decreased fat digestion and absorption may be associated with vitamin deficiences, including vitamin A. The aim of this study was to document plasma retinol binding protein (RBP) status, a specific plasma transport protein for vitamin A, and ocular surface changes in children and adolescents with CF. The patients were recruited at the 3rd Department of Paediatric Diseases, Medical University of Bialystok, Poland. All patients were regularly seen by a CF specialist dietitian. A group of 15 patients had the following investigations: plasma RBP, visual acuity, physical examination, tear film break-up time, fluorescein staining and Schirmer tear test. A group of 15 age- and sex-matched controls without CF or ocular pathology were also recruited. Plasma RBP concentrations were significantly lower in patients with CF than in the control group. CF patients showed a statistically significant increase in the incidence of clinical blepharitis. Five of the CF patients had clinical evidence of dry eyes. CONCLUSION: Low plasma retinol binding protein levels frequently occur in clinically stable and retinol supplemented cystic fibrosis patients, of whom five had dry eyes. We recommend monitoring of plasma retinol binding protein levels and evaluation of ocular surface changes, especially those with dry eye symptoms in all cystic fibrosis patients.


Subject(s)
Cystic Fibrosis/drug therapy , Retinol-Binding Proteins/metabolism , Vitamin A/therapeutic use , Xerophthalmia/drug therapy , Adolescent , Adult , Child , Cystic Fibrosis/blood , Cystic Fibrosis/metabolism , Female , Humans , Lung Volume Measurements , Male , Nutritional Status , Retinol-Binding Proteins, Plasma , Xerophthalmia/metabolism
19.
Public Health Nutr ; 6(3): 233-44, 2003 May.
Article in English | MEDLINE | ID: mdl-12740072

ABSTRACT

OBJECTIVES: The impact on vitamin A status of the distribution of vitamin A during national immunisation days (NIDs) has not been well established despite strong promotion by international agencies and donors. Using a pre-post design, the change in prevalence of vitamin A deficiency was examined in pre-school children in Mali. DESIGN: Two cross-sectional surveys were conducted in Mopti region, the first in March 1997 before this strategy was adopted and the second in March 1999, four-and-a-half months after a mass distribution of vitamin A during NIDs. SUBJECTS AND SETTING: We compared the vitamin A status of children aged 12 to 66 months targeted in 1999 by NIDs with the status of children in the same age group in 1997. Infectious events of the previous two weeks were concurrently recorded. Within the 1999 sample, the status of recipient and non-recipient children was also compared. RESULTS: In 1997, the prevalence of xerophthalmia (defined by the presence of night blindness and/or Bitot spots) was 6.9% (95% confidence interval (CI) 5.1-9.2) and the modified retinol dose response (MRDR) test proved abnormal in 77.8% of 12-66-month-old children (95% CI 68.27-85.17). In 1999 this picture had improved significantly, both for xerophthalmia prevalence, 3.3% (95% CI 2.1-5.2), and abnormal MRDR test response, 63.1% (95% CI 54.25-71.23). The infectious morbidity rates between 1997 and 1999 tended to decrease. No significant improvement was found among children older than those targeted by NIDs. In 1999, children who received vitamin A had a lower risk for xerophthalmia (3.0% for recipients vs. 8.7% for non-recipients) and experienced fewer infectious events. CONCLUSIONS: The clinical and biological vitamin A status of pre-school children improved between 1997 and 1999. Mass distribution of vitamin A appears to reduce the occurrence of xerophthalmia and would seem to be associated with a decrease in other related illnesses. Vitamin A supplementation during NIDs should be given a high priority when vitamin A deficiency remains a public health problem.


Subject(s)
Child Nutrition Disorders/epidemiology , Vitamin A Deficiency/epidemiology , Vitamin A/administration & dosage , Xerophthalmia/epidemiology , Anthropometry , Child Nutrition Disorders/drug therapy , Child, Preschool , Cross-Sectional Studies , Dietary Supplements , Female , Humans , Infant , Male , Mali/epidemiology , Night Blindness/drug therapy , Night Blindness/epidemiology , Nutrition Surveys , Prevalence , Treatment Outcome , Vitamin A/therapeutic use , Vitamin A Deficiency/drug therapy , Xerophthalmia/drug therapy
20.
East Afr Med J ; 80(1): 17-21, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12755237

ABSTRACT

OBJECTIVE: To determine the impact of vitamin A supplementation on child morbidity and nutritional status. DESIGN: A community based follow-up (interventional) in nature. SETTING: Two randomly selected Weredas (districts) of Tigray, North Ethiopia were studied between 1996 and 1997. SUBJECTS: Four thousand seven hundred and seventy children aged between six and 72 months, selected using a multi-stage sampling procedure were enrolled and clinically assessed for xerophthalmia and nutritional status. A sub-sample of these children (n = 281) was further assessed for their serum retinol levels. MAIN OUTCOME MEASURES: The pre and post intervention data on xerophthalmia, morbidity, nutritional status and serum retinol levels were compared. RESULTS: Vitamin A capsule coverage of 87% in all the villages of the Weredas and a statistically significant (p < 0.05) reduction in the prevalence of Bitot's spot (from 1.5 to 0.5), fever (from 29.8 to 14.2), diarrhoea (from 30.2 to 18.2), oedema (from 9.2 to 3.2), measles (from 14.0 to 6.2), conjunctivitis (from 10.2 to 3.0), stunted (from 64.2 to 42.7), wasted (from 12.8 to 2.5) and underweight (from 46.2 to 24.2). The proportion of children with normal serum retinol concentration (> 0.7 micromole/L) has also improved significantly (from 36.8 to 56.2). CONCLUSION: In conclusion, the significant improvement in morbidity and nutritional status that followed the intervention programme although encouraging, it still indicates the importance of coupling periodic provision of Vitamin A capsules with nutrition education.


Subject(s)
Dietary Supplements , Nutritional Status , Vitamin A Deficiency/drug therapy , Vitamin A/therapeutic use , Xerophthalmia/drug therapy , Child , Child, Preschool , Cross-Sectional Studies , Ethiopia/epidemiology , Humans , Infant , Sampling Studies , Vitamin A/blood , Vitamin A Deficiency/epidemiology , Xerophthalmia/epidemiology
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