Okruszko Michał Andrzej, Szabłowski Maciej, Zarzecki Mateusz, Michnowska-Kobylińska Magdalena, Lisowski Łukasz, Łapińska Magda, Stachurska Zofia, Szpakowicz Anna, Kamiński Karol Adam, Konopińska Joanna
Department of Ophthalmology, Medical University of Bialystok, Białystok, 15-089, Poland.
Department of Population Medicine and Lifestyle Diseases Prevention, Medical University of Białystok, Białystok, Poland.
J Inflamm Res. 2024 Feb 13;17:1021-1037. doi: 10.2147/JIR.S434989. eCollection 2024.
Glaucoma is the most common optic neuropathy and the leading cause of irreversible blindness worldwide, which affects 3.54% of the population aged 40-80 years. Despite numerous published studies, some aspects of glaucoma pathogenesis, serum biomarkers, and their potential link with other diseases remain unclear. Recent articles have proposed that autoimmune, oxidative stress and inflammation may be involved in the pathogenesis of glaucoma.
We investigated the serum expression of 92 inflammatory and neurotrophic factors in glaucoma patients. The study group consisted of 26 glaucoma patients and 192 healthy subjects based on digital fundography.
Patients with glaucoma had significantly lower serum expression of IL-2Rβ, TWEAK, CX3CL1, CD6, CD5, LAP TGF-beta1, LIF-R, TRAIL, NT-3, and CCL23 and significantly higher expression of IL-22Rα1.
Our results indicate that patients with glaucoma tend to have lower levels of neuroprotective proteins and higher levels of neuroinflammatory proteins, similar to those observed in psychiatric, neurodegenerative and autoimmune diseases, indicating a potential link between these conditions and glaucoma pathogenesis.
青光眼是最常见的视神经病变,也是全球不可逆性失明的主要原因,影响40至80岁人群中的3.54%。尽管已有大量研究发表,但青光眼发病机制、血清生物标志物及其与其他疾病的潜在联系的某些方面仍不清楚。最近的文章提出,自身免疫、氧化应激和炎症可能参与青光眼的发病机制。
我们研究了青光眼患者血清中92种炎症和神经营养因子的表达情况。基于数字眼底造影,研究组包括26例青光眼患者和192名健康受试者。
青光眼患者血清中IL-2Rβ、TWEAK、CX3CL1、CD6、CD5、LAP TGF-β1、LIF-R、TRAIL、NT-3和CCL23的表达显著降低,而IL-22Rα1的表达显著升高。
我们的结果表明,青光眼患者往往具有较低水平的神经保护蛋白和较高水平的神经炎症蛋白,这与在精神疾病、神经退行性疾病和自身免疫性疾病中观察到的情况相似,表明这些疾病与青光眼发病机制之间存在潜在联系。