Department of Ophthalmology, Miami Veterans Affairs Medical Center.
Bascom Palmer Eye Institute, University of Miami.
Curr Opin Ophthalmol. 2021 Jul 1;32(4):348-361. doi: 10.1097/ICU.0000000000000768.
Dry eye disease (DED) is a multifactorial disease affecting approximately 5-50% of individuals in various populations. Contributors to DED include, but are not limited to, lacrimal gland hypofunction, meibomian gland dysfunction (MGD), ocular surface inflammation, and corneal nerve dysfunction. Current DED treatments target some facets of the disease, such as ocular surface inflammation, but not all individuals experience adequate symptom relief. As such, this review focuses on alternative and adjunct approaches that are being explored to target underlying contributors to DED.
Neuromodulation, stem cell treatments, and oral royal jelly have all been studied in individuals with DED and lacrimal gland hypofunction, with promising results. In individuals with MGD, devices that provide eyelid warming or intense pulsed light therapy may reduce DED symptoms and signs, as may topical Manuka honey. For those with ocular surface inflammation, naturally derived anti-inflammatory agents may be helpful, with the compound trehalose being farthest along in the process of investigation. Nerve growth factor, blood-derived products, corneal neurotization, and to a lesser degree, fatty acids have been studied in individuals with DED and neurotrophic keratitis (i.e. corneal nerve hyposensitivity). Various adjuvant therapies have been investigated in individuals with DED with neuropathic pain (i.e. corneal nerve hypersensitivity) including nerve blocks, neurostimulation, botulinum toxin, and acupuncture, although study numbers and design are generally weaker than for the other DED sub-types.
Several alternatives and adjunct DED therapies are being investigated that target various aspects of disease. For many, more robust studies are required to assess their sustainability and applicability.
干眼(DED)是一种多因素疾病,影响各种人群中约 5-50%的个体。DED 的发病因素包括但不限于泪腺功能低下、睑板腺功能障碍(MGD)、眼表炎症和角膜神经功能障碍。目前的 DED 治疗方法针对疾病的某些方面,如眼表炎症,但并非所有患者都能获得足够的症状缓解。因此,本综述重点关注正在探索的针对 DED 潜在发病因素的替代和辅助治疗方法。
神经调节、干细胞治疗和口服蜂王浆已在 DED 和泪腺功能低下患者中进行了研究,结果令人鼓舞。对于 MGD 患者,提供眼睑温暖或强脉冲光治疗的设备可能会减轻 DED 症状和体征,局部使用麦卢卡蜂蜜也可能有帮助。对于眼表炎症患者,天然抗炎剂可能会有所帮助,其中海藻糖的研究进展最为深入。神经生长因子、血液衍生产品、角膜神经再支配以及在较小程度上的脂肪酸已在 DED 和神经营养性角膜炎(即角膜神经感觉减退)患者中进行了研究。在 DED 合并神经病理性疼痛(即角膜神经感觉过敏)患者中,包括神经阻滞、神经刺激、肉毒杆菌毒素和针灸在内的各种辅助治疗方法已被研究,尽管这些研究的数量和设计通常不如其他 DED 亚型那么强。
正在研究几种替代和辅助 DED 治疗方法,这些方法针对疾病的各个方面。对于许多方法,需要进行更强大的研究来评估其可持续性和适用性。