Bourguet Aurélie, Chaudieu Gilles, Briatta Alice, Guyonnet Alexandre, Abitbol Marie, Chahory Sabine
Ophthalmology Unit, Ecole Nationale Vétérinaire d'Alfort, Université Paris-Est, 7 Avenue du Général de Gaulle, 94700, Maisons-Alfort Cedex, France.
Clinique Vétérinaire, 52 boulevard M. Pourchon, Clermont-Ferrand, 63100, France.
Vet Ophthalmol. 2018 Jan;21(1):10-18. doi: 10.1111/vop.12470. Epub 2017 Apr 25.
To document the clinical appearance and prevalence of cataracts in a French population of Bengal cats.
Two distinct populations of Bengal cats were examined as follows: (i) 51 animals recruited for evaluation of national prevalence of ocular diseases in an observational study conducted between October 2014 and November 2016 at the Alfort ophthalmology unit; (ii) 12 patients referred for cataract diagnosis examined at a veterinary eye clinic located in central France, between December 2014 and February 2016. Buccal swabs or blood samples for DNA analysis were collected from all patients. The pedigrees of the examined Bengal cats were also investigated.
Cataracts were diagnosed in 23 of 51 (45%) cats in the observational study and in all cats in the referral population, mostly bilaterally. Visual impairment was never reported. Age of subjects affected by cataracts ranged from 3 months to 9.6 years (median: 1.9 years). Cataracts were classified as nuclear cataracts (14 of 23 in the observational group and 12 of 12 in the referral group) with a focal, perinuclear, posterior, or complete nuclear pattern, or posterior polar subcapsular cataracts (10 of 23 only in the observational group). An inherited congenital origin appears to be the most likely hypothesis. The pedigree analysis suggests a hereditary component of cataract formation, but further analyses in a larger population or test matings are needed to determine the exact mode of inheritance.
Presumed inherited cataracts appear to have a high prevalence in Bengal cats in France. The main manifestations are nuclear or subcapsular form, mostly bilateral, symmetrical, and apparently nonprogressive.
记录法国孟加拉猫群体中白内障的临床表现及患病率。
对两个不同的孟加拉猫群体进行了如下检查:(i)在2014年10月至2016年11月于阿尔福特眼科部门进行的一项观察性研究中招募的51只用于评估全国眼部疾病患病率的动物;(ii)2014年12月至2016年2月期间在法国中部一家兽医眼科诊所接受白内障诊断检查的12只猫。从所有猫身上采集颊拭子或血液样本用于DNA分析。还对所检查的孟加拉猫的系谱进行了调查。
在观察性研究的51只猫中有23只(45%)被诊断患有白内障,在转诊群体的所有猫中均诊断出白内障,大多数为双侧性。从未报告有视力障碍。受白内障影响的猫的年龄范围为3个月至9.6岁(中位数:1.9岁)。白内障被分类为核性白内障(观察组23只中有14只,转诊组12只中有12只),具有局灶性、核周性、后极性或完全核性模式,或后极性囊下白内障(仅观察组23只中有10只)。遗传先天性起源似乎是最有可能的假设。系谱分析表明白内障形成有遗传因素,但需要在更大的群体中进行进一步分析或进行测交来确定确切的遗传方式。
在法国的孟加拉猫中,推测遗传性白内障似乎患病率很高。主要表现为核性或囊下型,大多为双侧性、对称性,且显然无进展性。