Dogru M, Katakami C, Nakagawa N, Tetsumoto K, Yamamoto M
Department of Ophthalmology, Kobe University School of Medicine, Japan.
Ophthalmology. 1998 Aug;105(8):1478-84. doi: 10.1016/S0161-6420(98)98032-0.
This study aimed to describe the ocular surface disorder in patients with atopic dermatitis (AD).
A prospective case-controlled study.
A total of 44 patients with active AD seen at Kobe University School of Medicine, Department of Ophthalmology, during 1994 through 1996 and 22 normal control subjects were studied.
The subjects underwent routine ophthalmic examinations, tear film break-up time (BUT), Schirmer test, and conjunctival impression cytology.
Patients and control subjects were compared for tear function parameters, goblet cell density, and conjunctival squamous metaplasia grade. The relation of duration and recurrences of AD to the ocular surface disorder also was looked for.
The duration of atopic disease ranged from 18 to 32 years (mean, 22.8 years). The average for exacerbations was 4.5 times. Chronic allergic conjunctivitis with superficial punctate keratitis was the most frequent clinical presentation. The BUT and Schirmer test values were significantly lower in patients with AD compared with those of the control subjects. Impression cytology showed goblet cell loss and conjunctival squamous metaplasia, both of which related to the number of recurrences of AD rather than the duration of disease. Facial atopy and allergic keratoconjunctivitis (AKC) related to the metaplasia of the ocular surface (P < 0.001). Patients with reduced goblet cell density also showed low BUT levels (P < 0.001).
Ocular surface disorder of AD characterized by goblet cell loss and conjunctival squamous metaplasia seemed to evolve independently of the duration of disease but worsen with increased number of flare-ups. Direct epithelial damage by the allergic reaction, disorder of tear quality, and quantity may be important in the genesis of the atopic ocular surface disease.
本研究旨在描述特应性皮炎(AD)患者的眼表疾病。
一项前瞻性病例对照研究。
1994年至1996年期间在神户大学医学院眼科就诊的44例活动性AD患者和22例正常对照者参与了研究。
受试者接受常规眼科检查、泪膜破裂时间(BUT)、泪液分泌试验及结膜印迹细胞学检查。
比较患者和对照者的泪液功能参数、杯状细胞密度及结膜鳞状化生分级。同时观察AD病程及复发次数与眼表疾病的关系。
特应性疾病病程为18至32年(平均22.8年)。平均发作次数为4.5次。慢性过敏性结膜炎伴浅层点状角膜炎是最常见的临床表现。AD患者的BUT和泪液分泌试验值显著低于对照者。印迹细胞学检查显示杯状细胞缺失和结膜鳞状化生,二者均与AD复发次数有关,而非疾病病程。面部特应性和变应性角结膜炎(AKC)与眼表化生有关(P < 0.001)。杯状细胞密度降低的患者BUT水平也较低(P < 0.001)。
以杯状细胞缺失和结膜鳞状化生为特征的AD眼表疾病似乎独立于疾病病程发展,但随着发作次数增加而恶化。过敏反应导致的直接上皮损伤、泪液质量和量的紊乱可能在特应性眼表疾病的发生中起重要作用。