O presente trabalho tem por objetivo analisar o efeito do metilmercúrio na retina de peixe tropical Hoplias malabaricus (Traíra) através de baixas doses agudas. As intoxicações foram realizadas, por meio de injeção intraperitoneal, nas doses de 0,01, 0,05, 0,1 e 1,0 g/g, com um período de quinze dias de depuração do MeHg. Após o término do período de depuração, os olhos foram enucleados e as retinas isoladas foram fixadas em PFA 4% por 3 horas. As retinas foram conservadas, até o momento do uso (ou por no mínimo 9 horas), em tampão PB 0,1M a 4ºC. Após os procedimentos imunohistoquímicos para marcação de células bipolares do tipo ON com estratificação na sublâmina b da CPI, as retinas foram aplanadas para confecção de montagens planas para a análise quantitativa de células bipolares ON imunorreativas a proteína cinase C _. A análise quantitativa das células da camada de células ganglionares (CCG) também foi realizada. Células da CCG foram coradas pela técnica de Nissl, as retinas foram aplanadas em lâminas gelatinizadas e submetidas a uma bateria de desidratação (com diferentes concentrações alcoólicas) e coloração, utilizando cresil violeta como corante. Estas análises foram realizadas em 3 ou 4 retinas para cada dose testada. Análises idênticas foram realizadas nas retinas controle. Todas as retinas foram dividas nos quadrantes dorsal, ventral, nasal, temporal e em centro e periferia. Campos foram fotografados por toda a retina com intervalos de 1 mm, com auxilio do programa Axio Vision por meio de uma câmera digital e um microscópio acoplados a um computador. Os campos amostrados foram contados com o auxilio do programa NIH Scion Imagem 2.0. A densidade média de células foi estimada para cada retina e os grupos intoxicados foram comparados com o grupo controle (Teste T-student). A partir dos dados de densidade celular, mapas de isodensidade foram confeccionados, além de permitir estimar o poder de resolução teórico da acuidade visual de cada um dos animais experimentais utilizados para análise de células da CCG a partir da densidade máxima de células. Evidenciamos que as baixas doses agudas testadas não causam diminuição na densidade célular de células bipolares ON e células da CCG, comparado ao grupo controle. Não houve reduções significativas na densidade de células para ambos os tipos celulares analizados em nenhuma das regiões retinianas nas doses de MeHg testadas. Assim, a intoxicação de MeHg por baixas doses agudas não alterou o poder de resolução teorio da acuiade visual dos animais testados / This study aims to examine the effects of low acute doses of methylmercury (MeHg) on the retina of the tropical fish Hoplias malabaricus (Thraira). Four levels of MeHg intoxication were induced by intraperitoneal injection of doses of either 0.01, 0.05, 0.1 or 1.0 g MeHg/g of body weight, followed by a fifteen day period of depuration of MeHg. After the depuration period, the eyes were harvested, and the retinas were isolated and fixed in 4% paraformaldehyde for 3 hours. The retinas were then stored (for at least for 9 hours) in 0.1 M sodium phosphate PB buffer at 4°C until the time of analysis. ON bipolar cells in sublamina b of the inner plexiform layer immunoreactive to protein Kinase C_ were immunohistochemically labeled, and the retinas were flattened to make whole mounts for quantitative analysis of ON bipolar cell densities. Quantitative analysis of cells in the retinal ganglion cell layer (GCL) was also performed. GCL cells were Nissl stained, and the retinas were flattened on gelatinized slides and subjected to another battery of dehydration (with different alcohol concentrations) and staining using cresyl violet. These analyses were carried out in 3 or 4 retinas for each dose tested. Identical analyses were performed on the control retinas. All retinas were divided into regions: dorsal, ventral, nasal, temporal, center and periphery. Sample retinal fields were photographed throughout the retina at intervals of 1 mm, with a digital camera attached to a microscope using Axio Vision software coupled to a computer. ON bipolar and GCL cells within the fields were counted with the help of the NIH Scion Image 2.0 software. The average density (mm2) of both types of cells was estimated for each retina and the data from each of the four MeHgintoxicated groups were compared with the control group values (Student t-test). From the density data we derived isodensity maps, permitting us to estimate the theoretical resolving power (maximum visual acuity) of each of the experimental animals used from the maximum density of cells in the ganglion cell layer. We showed that low acute doses of MeHg/g do not decrease cell densities of either ON bipolar cells or cells in the GCL, compared to controls. There were no significant decreases in cell density (counts) for either cell type in any of the retinal regions, for any of the MeHg doses tested. Thus, acute low-dose MeHg intoxication did not degrade the estimates of the animals theoretical resolving power

A prematuridade ao nascimento é um fator de risco para a visão, podendo causar retinopatia, uma condição em que há descolamento da retina. Retinopatia da prematuridade ocorre em uma parcela relativamente pequena dos recém nascidos prematuros e não sabemos se os demais, cujo desenvolvimento visual é aparentemente normal, seguem de fato o mesmo curso que o observado em bebes nascidos após uma gestação completa, ou se também sofrem algum prejuízo devido ao nascimento prematuro. Alternativamente, estes bebês poderiam ter um desenvolvimento visual acelerado pela sua exposição mais longa ao mundo visual. Para saber se a condição de prematuridade acelera, retarda, ou não altera o desenvolvimento da visão, o presente trabalho comparou o desenvolvimento das funções de acuidade visual e de sensibilidade ao contraste espacial de luminância em bebês nascidos prematuros e a termo. O estudo utilizou o método dos Potenciais Visuais Corticais Provocados de Varredura para examinar essas funções. Possíveis correlações entre os limiares visuais obtidos durante o primeiro ano de vida e idade gestacional, índices de Apgar, e valores de peso ao nascimento, foram examinadas. Os participantes foram 57 bebês de ambos os sexos encaminhados pelo Hospital Universitário da Universidade de São Paulo, dos quais 31 prematuros e 26 nascidos a termo. As avaliações foram realizadas principalmente em 3 fases do desenvolvimento visual: 4, 6 e 12 meses de vida. Os bebês prematuros tiveram suas idades corrigidas com relação à idade gestacional para a comparação com os grupos de termos. Um grupo de 14 sujeitos adultos também foi avaliado com os mesmos estímulos visuais. As avaliações das funções de acuidade visual e sensibilidade ao contraste foram realizadas através do método de potenciais visuais corticais provocados de varredura. Eletrodos posicionados no escalpo da região occipital dos pacientes captaram as respostas eletrofisiológicas provocadas por estímulos gerados em um monitor de alta resolução por um sistema computadorizado (sistema NuDiva). Estes estímulos consistiam de grades quadradas com valor de contraste fixo (80%) para avaliação da acuidade visual, e grades senoidais de 4 freqüências espaciais: 0,2 , 0,8 , 2,0 e 4,0 ciclos por grau para a avaliação da sensibilidade ao contraste. Prematuros e termos não apresentaram diferenças estatísticas significantes nas funções visuais avaliadas em nenhuma fase do desenvolvimento. O pico de sensibilidade ao contraste ocorreu entre .8 e 2.0 cpg de 4 meses de idade. No sexto mês o pico deslocou-se para 2.0 cpg, e entre os meses 9 e 12 passou para freqüências espaciais mais altas, por volta de 4.0 cpg coincidindo com o pico encontrado para os adultos. Nossos dados sugerem que nem a experiência visual, maior nos prematuros em relação aos termos, nem o tempo de gestação, maior nos termos em relação aos prematuros, afetam o desenvolvimento da visão espacial em humanos. / Prematurity at birth is a risk factor for vision, since it may lead to retinopathy - a condition in which there is retinal detachment. Retinopathy of prematurity occurs in a relatively small percentage of premature infants and it is not known if the remainder, whose visual development is apparently normal, follow the same course as in term babies after a complete gestational period, or if they also suffer some loss from having been born before complete development. Alternatively, these babies might have an accelerated visual development due to their longer exposure to the visual world, compared to term babies. To examine if prematurity accelerates, slows down, or does not affect visual development, the present study compared the development of visual acuity and contrast sensitivity in premature and term babies. The study used the methodology of the sweep visual evoked potentials to examine these functions. Possible correlations between visual thresholds obtained during the first year of life and gestational age, apgar index and birth weight, were examined. Participants were 57 infants of both genders, recruited by the University Hospital of São Paulo University, of which 31 were prematurely born and 26 were term infants. Evaluations were performed at three visual developmental epochs: 4, 6 e 12 months of age. The age of preterm infants was corrected by their gestational ages in order to allow comparison with the term infants. Another group with 14 adult subjects was tested with the same visual stimulus. Visual acuity and contrast sensitivity tests were performed with the sweep visual evoked potential method. Electrodes placed over the infant\'s scalp at the occipital role recorded electrophysiological responses evoked to visual stimuli generated by a high resolution monitor of a computerized system. The stimuli were square wave gratings with 80% of contrast to evaluate visual acuity, and sine wave gratings of 4 spatial frequencies: 0,2 , 0,8 , 2,0 e 4,0 cycles per degree to evaluate contrast sensitivity. Preterm and term infants did not show statistical differences in the evaluated visual functions in any developmental phase. The contrast sensitivity peak occurred between 0.8 and 2.0 cpd at 4 months of age. At the sixth month the peak moved to 2.0 cpd and it was displaced to a higher spatial frequency (4.0 cpd) at 12 months, where it coincides with the adult SCS peak. Our data suggest that neither visual experience, longer in the preterm, nor gestational age, longer in the term infants, seems to affect spatial vision functions in humans.

Orientadores: Abimael Aranha Netto, André Moreno Morcillo / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas / Made available in DSpace on 2018-08-21T16:08:29Z (GMT). No. of bitstreams: 1 Martini_Giovana_M.pdf: 6946196 bytes, checksum: 0958a806379064012236749e08f7a700 (MD5) Previous issue date: 2012 / Resumo: Objetivos: Determinar o desenvolvimento da acuidade visual de grades binocular e monocular, mensuradas com o Lea Gratings, prover uma base idade-dependente por esta técnica em uma coorte de crianças saudáveis e comparar os resultados obtidos por este teste com os obtidos com os Cartões de Acuidade de Teller. Método: Tratou-se de estudo prospectivo e longitudinal, descritivo e analítico, da acuidade visual de resolução de grades de um grupo de lactentes, nos três primeiros meses de vida e no período entre 12 e 24 meses. Considerou-se, como critérios de inclusão, lactentes que foram nascidos a termo e adequados para a idade gestacional, com um mês de idade cronológica e residentes na região metropolitana de Campinas, que apresentaram o Reflexo Vermelho presente ao nascimento. A acuidade visual de resolução de grades foi mensurada por meio do teste Lea Gratings, mês a mês, e, a partir dos 12 meses, também por meio dos Cartões de Acuidade de Teller, quando foram descartadas alterações oftalmológicas nos participantes do estudo. A amostra foi constituída de 133 lactentes e a análise dos resultados foi realizada utilizando-se o Statistical Package for Social Sciences for Personal Computer (SPSS 16.0). Os valores de acuidade (CPD) foram apresentados em distribuição de frequência e para determinação da média e do desvio padrão, os dados foram transformados em escala de uma oitava. Para comparação da acuidade visual entre as idades foi utilizada a análise de variância para medidas repetidas e o de Wilcoxon para comparação das medidas entre os olhos para amostras relacionadas. A correlação entre os resultados obtidos pelos dois testes foi avaliada pelo Coeficiente de Correlação de Spearman. Resultados: Os valores de acuidade visual binocular foram crescentes, sendo obtida no primeiro mês a média de 0,55 cpd (±0,70), de 1,35 cpd (±0,69) no segundo mês e de 3,11 cpd (±0,54) no terceiro mês. A partir dos 12 meses, as médias dos valores de acuidade visual binocular e monocular - foram, respectivamente, de 14,41 cpd (±0,25) e de 12,03 cpd (±0,39) nas crianças com idade entre 12 e 14 meses, de 14,10 cpd (±0,27) e de 10,79 cpd (±0,42) em crianças com idade entre 15 e 18 meses e de 15,50 cpd (±0,13) e de 13,42 cpd (±0,26) em crianças com idade entre 19 e 24 meses. Os resultados da análise de variância demonstraram diferenças significativas nos valores de acuidade visual entre todas as idades. Os coeficientes de Correlação de Spearman entre os testes Lea Gratings e Cartões de Acuidade de Teller foram de 0,53505 e de 0,65175 para, respectivamente, as medidas binocular e monocular. Conclusão: O teste foi capaz de avaliar a evolução da acuidade visual no primeiro trimestre de vida e no período entre 12 a 24 meses, e permitiu o fornecimento de uma base idade-dependente por esta técnica em uma coorte de lactentes saudáveis até o período de 12 meses. A comparação entre os dois testes de acuidade visual de grades demonstrou correlação positiva / Abstract: Purpose: This study aims to determine the development of the binocular and monocular grating acuity with Lea Gratings, to established age-related norms for this method in a health children cohort and comparing the results obtained by this test with those obtained with the Teller Acuity Cards. Methods: This was a prospective and longitudinal study, descriptive and analytic, of infant grating visual acuity in the first three months of life and between the ages 12 and 24 months. The sample was composed of infants that met the following criteria: full-term infants appropriate for gestational age, with a chronological age of one month, residents in the Campinas metropolitan region, born with positive red reflex and whose parents consented to participate in this study. The grating acuity of each infant was measured three times at regular intervals, using Lea Gratings, and after 12 months, also with the Teller Acuity Cards, when a complete ophthalmologic examination was conducted to reject any visual alteration. The final sample was composed of 133 infants and the results were analyzed with the Package for Social Sciences for the Personal Computer (SPSS 16.0). The grating acuity results were stated in frequency tables and converted into a one-octave scale for statistical calculation. Repeated measure analysis of variance was applied to compare the grating acuity results among ages. The Wilcoxon test was used to compare the measures between the eyes in related samples and the Spearman Correlation was applied to evaluate the results obtained with the two tests. Results: The binocular grating acuity measures were crescent. In the first month, the mean acuity was 0.55 cpd (±0.70); in the second month, the mean acuity was 1.35 cpd (±0.69) and in the third month it was 3.11 (±0.54). After 12 months, the means of binocular and monocular acuity were, respectively, 14.41 cpd (±0.25) and 12.03 cpd (±0.39) in children between ages 12 and 14 months; 14.10 cpd (±0.27) and 10.79 cpd (±0.42) in children between ages 15 and 18 months; 15.50 cpd (±0.13) and 13.42 cpd (±0.26) in children between ages 19 and 24 months. Analysis of variance to repeated measures indicated differences between the measures of grating acuity in all ages. The coefficient of Spearman Correlation between the tests Lea Gratings and Teller Acuity Cards was respectively 0.53505 and 0.65175 for binocular and monocular measures. Conclusions: This test was capable to assess the evolution of grating acuity in the first three months of life and between 12 and 24 months, and established age-related norms for this method in a health children cohort until 12 months age. The comparison between the two tests of grating acuity demonstrated positive correlation / Mestrado / Saude da Criança e do Adolescente / Mestra em Saúde da Criança e do Adolescente

In this study we examined dynamic visual acuity as a functional testing of the vestibulo- ocular reflex. Two groups were examined: 22 healthy seniors and 22 healthy young people as controls. We used two types of situations for testing: while walking on a treadmill at a speed of 2, 4 and 5 kmph, and with a subject's head passively moved in yaw and pitch plane. Visual acuity was measured with optotype charts (for the walking test it was a standard Snellen optotype chart at 6 m distance, for the test of head moves it was a Jaeger chart at 30 cm distance). The values obtained in these ways we related to values of a subject's static visual acuity, measured in the same conditions, just before the dynamic situations were examined. We found significant difference of dynamic visual acuity in senior group within each condition tested. We also found a significant decline as for difference of dynamic visual acuity in the senior group compared to young subjects - in the walking test at 4 and 5 kmph and in both head-moving conditions. These results indicate age-related impairment in function of vestibulo-ocular reflex. Based on our results, the test of passive head moves appears to be more suitable for ordinary clinical examination of dynamic visual acuity.

Il est connu que le cannabis, par son action sur le système endocannabinoïde, affecte de multiples paramètres de la vision. Les fonctions de GPR55, un récepteur associé au système endocannabinoïde, ont moins été étudiées que celles des récepteurs cannabinoïdes les plus importants, CB1 et CB2. Nous savons cependant que GPR55 est présent dans la rétine de la souris et qu’il module la croissance et le guidage axonal des cellules ganglionnaires rétiniennes durant le développement. Le but de cette étude est d’étudier les effets de GPR55 sur la vision en utilisant un modèle de souris avec une délétion du gène Gpr55. Des électrorétinographies (ERG) plein champ scotopique et photopique ont été effectuées dans le but d’étudier le rôle du récepteur sur les fonctions rétiniennes. Nous avons trouvé que les souris Gpr55-/- ont, en ERG scotopique, une amplitude réduite de l’onde-b et des potentiels oscillatoires qui ont aussi une latence plus longue. Chez ces animaux, l’onde-a photopique a aussi une amplitude plus basse. Par la suite, pour vérifier les conséquences des déficits de fonction rétinienne sur les fonctions visuelles, le modèle de réflexe optomoteur a été utilisé sur des souris knock-out ou avec des injections systémiques d’un antagoniste et d’un agoniste de GPR55. L’absence de GPR55 retarde le développement de l’acuité visuelle, mais la délétion de Gpr55 ou l’action pharmacologique sur le récepteur ne change pas l’acuité visuelle chez les adultes. La délétion de Gpr55 et l’administration d’un antagoniste du récepteur diminuent la sensibilité au contraste. Ces observations suggèrent que GPR55 peut modifier l'activité des cônes, des cellules bipolaires et des cellules de la rétine interne avec des conséquences comportementales. / The observations on how cannabis affects multiple properties of vision have fostered the interest in the study of the functions of cannabinoid receptors CB1 and CB2 in the visual system. However, other non-classical cannabinoid receptors are thought to be involved in mediating the actions of cannabinoid ligands in the eye. One of these candidate receptors is GPR55, a receptor that modulates the growth and axonal guidance of retinal ganglion cells during development in mice. The purpose of this study was to investigate the effects of the deletion of the Gpr55 gene and the pharmacological modulation of GPR55 on retinal function and visual behavior. Full-field scotopic and photopic electroretinography (ERG) were used to functionally assess the state of the retina. Recordings obtained from Gpr55-/- mice revealed a diminution of the scotopic b-wave and the photopic a-wave responses. These animals also had reduced and delayed oscillatory potentials. The optomotor reflex method was used to evaluate the consequences of Gpr55 deletion on visual acuity and contrast sensitivity. The absence of GPR55 delayed the developmental trajectory of visual acuity in Gpr55 knockout mice without affecting the maximum visual acuity reached in adulthood. Pharmacological manipulation of GPR55 in adult wild-type mice did not alter visual acuity. Both the deletion of Gpr55 and the administration of a receptor antagonist decreased contrast sensitivity while an agonist of GPR55 increased contrast sensitivity. These observations suggest that GPR55 can modify the activity of cones, bipolar cells, and cells in the inner retina with behavioral consequences.

No / PURPOSE: A computer-based interactive binocular treatment system (I-BiT) for amblyopia has been developed, which utilises commercially available 3D 'shutter glasses'. The purpose of this pilot study was to report the effect of treatment on visual acuity (VA) in children with amblyopia. METHODS: Thirty minutes of I-BiT treatment was given once weekly for 6 weeks. Treatment sessions consisted of playing a computer game and watching a DVD through the I-BiT system. VA was assessed at baseline, mid-treatment, at the end of treatment, and at 4 weeks post treatment. Standard summary statistics and an exploratory one-way analysis of variance (ANOVA) were performed. RESULTS: Ten patients were enrolled with strabismic, anisometropic, or mixed amblyopia. The mean age was 5.4 years. Nine patients (90%) completed the full course of I-BiT treatment with a mean improvement of 0.18 (SD=0.143). Six out of nine patients (67%) who completed the treatment showed a clinically significant improvement of 0.125 LogMAR units or more at follow-up. The exploratory one-way ANOVA showed an overall effect over time (F=7.95, P=0.01). No adverse effects were reported. CONCLUSION: This small, uncontrolled study has shown VA gains with 3 hours of I-BiT treatment. Although it is recognised that this pilot study had significant limitations-it was unblinded, uncontrolled, and too small to permit formal statistical analysis-these results suggest that further investigation of I-BiT treatment is worthwhile.

No / To determine whether Hartmann-Shack wavefront sensing detects differences in optical performance in vivo between poly(methyl methacrylate) (PMMA) and foldable acrylic intraocular lenses (IOLs) and between clear corneal and scleral tunnel incisions and whether optical differences are manifested as differences in visual performance. SETTING: Department of Optometry, University of Bradford, West Yorkshire, United Kingdom. METHODS: This study comprised 74 subjects; 17 were phakic with no ocular pathology, 20 had implantation of a Pharmacia 722C PMMA IOL through a scleral tunnel, 21 had implantation of an Alcon AcrySof IOL through a scleral tunnel, and 16 had implantation of an AcrySof IOL through a corneal incision. Visual acuity and contrast sensitivity testing, ocular optical quality measurement using Hartmann-Shack wavefront sensing, and corneal surface measurement with a videokeratoscope were performed in all cases. RESULTS: There were significant differences between groups in the total root-mean-square (RMS) wavefront aberration over a 6.0 mm pupil (F=3.91; degrees of freedom=3,70; P<.05) mediated at the 4th-order RMS, specifically spherical and tetrafoil aberrations. The PMMA-scleral group had the least aberrations and the AcrySof-corneal group the most. For a 3.5 mm diameter pupil, the total higher-order RMS wavefront aberration was not significantly different between the groups (P>.05). There were no differences between groups in corneal shape, visual acuity, or contrast sensitivity. CONCLUSIONS: Implantation of the spherical PMMA IOL led to a slight reduction in total wavefront aberration compared to phakic eyes. AcrySof IOLs induced more aberrations, especially spherical aberration. Corneal-based incisions for IOL implantation compounded this increase. Studies of the optical performance of IOLs in vivo should use wavefront sensing as the main outcome measure rather than visual measures, which are readily confounded by multiple factors.

京都大学 / 新制・課程博士 / 博士(医学) / 甲第25159号 / 医博第5045号 / 新制||医||1070(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 中山 健夫, 教授 森田 智視, 教授 永井 洋士 / 学位規則第4条第1項該当 / Doctor of Agricultural Science / Kyoto University / DFAM

No / To determine the test-retest reliability of the Randot stereoacuity test when used as part of vision screening in schools. METHODS: Randot stereoacuity (graded-circles) and logMAR visual acuity measures were gathered in an unselected sample of 139 children (aged 4-12, mean 8.1+/-2.1 years) in two schools. Randot testing was repeated on two occasions (average interval between successive tests 8 days, range: 1-21 days). Three Randot scores were obtained in 97.8% of children. RESULTS: Randot stereoacuity improved by an average of one plate (ie, one test level) on repeat testing but was little changed when tested on the third occasion. Within-subject variability was up to three test levels on repeat testing. When stereoacuity was categorised as 'fine', 'intermediate' or 'coarse', the greatest variability was found among younger children who exhibited 'intermediate' or 'coarse'/nil stereopsis on initial testing. Whereas 90.8% of children with 'fine' stereopsis (</=50 arc-seconds) on the first test exhibited 'fine' stereopsis on both subsequent tests, only approximately 16% of children with 'intermediate' (>50 but </=140 arc-seconds) or 'coarse'/nil (>/=200 arc-seconds) stereoacuity on initial testing exhibited stable test results on repeat testing. CONCLUSIONS: Children exhibiting abnormal stereoacuity on initial testing are very likely to exhibit a normal result when retested. The value of a single, abnormal Randot graded-circles stereoacuity measure from school screening is therefore questionable.

No / Postural instability in older people is associated with an increased risk of falling. This experiment investigated the effects of different gaze strategies on postural stability in older people, when using distance single-vision compared with multifocal (progressive addition lens and bifocal) spectacles. METHODS: Eighteen healthy older habitual multifocal spectacle-wearers (mean age 72.1 +/- 4.0 years) participated in a randomised, cross-over study. Postural stability during quiet standing was assessed as the root mean square excursion in the centre of pressure (RMS-COP) in the antero-posterior direction. Ground reaction force data were collected (for 30 seconds), while subjects viewed one of two visual targets (one square metre) of different spatial frequencies and contrasts, while wearing either distance single-vision or multifocal (progressive addition and bifocal) spectacles. The visual targets were positioned either ahead at eye-level or on the ground (viewing distance 2.06 metres) and viewed under the following head-gaze conditions; 'head neutral-gaze forward', 'head flexed-gaze down' and 'head neutral-gaze down'. RESULTS: The type of spectacles worn or the target viewed had no significant effect on postural stability but postural stability deteriorated (antero-posterior RMS-COP excursion increased) in the 'head neutral-gaze down' compared with the 'head flexed-gaze down' and 'head neutral-gaze forward' conditions (5.9, 5.5 and 5.0 mm respectively, p < 0.001). CONCLUSIONS: Multifocal use had no effect on standing postural stability. Irrespective of spectacles worn, when fixating a visual target positioned at ground level, postural stability was better in the 'head flexed-gaze down' condition compared with the 'head neutral-gaze down' condition. A useful strategy to reduce falling in the older person might be to advise multifocal and distance single-vision spectacle-wearers to flex their heads rather than just lower their eyes when looking downwards.