Das Taraprasad, Takkar Brijesh, Padakandala Shalem R, Shivaji Sisinthy
Anant Bajaj Retina Institute, Srimati Kanuri Santhamma Centre for Vitreoretinal Diseases, LV Prasad Eye Institute, Hyderabad, Telangana, India.
IHOPE Research Centre, LV Prasad Eye Institute, Hyderabad, Telangana, India.
Indian J Ophthalmol. 2025 Jan 1;73(Suppl 1):S144-S150. doi: 10.4103/IJO.IJO_966_24. Epub 2024 Oct 25.
To explore the relationship between gut microbiome, gut mycobiome, and intraocular (aqueous humor) microbiome dysbiosis in people with type 2 diabetes (T2DM) and diabetic retinopathy (DR).
Multiple case-control studies.
We evaluated three groups of people: healthy controls (HC), people with T2DM without retinopathy, and those with DR. The study samples included fecal matter (30-50 g) and aqueous humor (0.05-0.1 mL). After amplicon sequencing, we analyzed microbiome profiles (V3-V4 region of bacterial 16S rRNA gene) and mycobiome (ITS2 region of fungal rRNA gene). The main outcome measures were relative abundance, α and β diversity, and dysbiotic bacteria and fungi, analyzed based on the inferred functions of the taxa.
We recruited 82 people for gut microbiome (30 HC, 24 DM, and 28 DR); 75 people for gut mycobiome (30 HC, 21 DM, and 24 DR); and 12 people for aqueous humor microbiome (4 each HC, DM, and DR) studies. Generally, there was an increased abundance of pro-inflammatory and pathogenic microorganisms and a decreased abundance of anti-inflammatory and probiotic microorganisms. The differences were higher between HC and DM/DR than between DM and DR. In aqueous humor, there was a wider separation in microbiome profiles of people with DR than their gut microbiome.
The gut and aqueous humor microbiota of people with diabetes and DR may differ from those without diabetes. Given these unique observations in individuals living in one region of India, further research involving people from different regions is required to identify indices for possible regional or global use.
探讨2型糖尿病(T2DM)和糖尿病视网膜病变(DR)患者肠道微生物群、肠道真菌群与眼内(房水)微生物群失调之间的关系。
多项病例对照研究。
我们评估了三组人群:健康对照者(HC)、无视网膜病变的T2DM患者以及患有DR的患者。研究样本包括粪便(30 - 50克)和房水(0.05 - 0.1毫升)。经过扩增子测序后,我们分析了微生物群谱(细菌16S rRNA基因的V3 - V4区域)和真菌群(真菌rRNA基因的ITS2区域)。主要观察指标为相对丰度、α和β多样性以及功能失调的细菌和真菌,并根据分类群的推断功能进行分析。
我们招募了82人进行肠道微生物群研究(30名HC、24名DM和28名DR);75人进行肠道真菌群研究(30名HC、21名DM和24名DR);12人进行房水微生物群研究(每组4名HC、DM和DR)。总体而言,促炎和致病微生物的丰度增加,抗炎和益生菌微生物的丰度降低。HC与DM/DR之间的差异高于DM与DR之间的差异。在房水中,DR患者的微生物群谱分离比其肠道微生物群更明显。
糖尿病和DR患者的肠道和房水微生物群可能与非糖尿病患者不同。鉴于在印度一个地区居民中的这些独特观察结果,需要对来自不同地区的人群进行进一步研究,以确定可能用于区域或全球的指标。