State Key Laboratory of Ophthalmology, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Department of Ophthalmology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China.
Int Ophthalmol. 2022 Jun;42(6):1927-1938. doi: 10.1007/s10792-021-02190-5. Epub 2022 Feb 11.
To explore the profile of gut microbiota and central carbon-related metabolites in patients with primary angle-closure glaucoma (PACG).
The fecal microbiotas of 30 PACG patients and 30 healthy participants were detected via 16S rRNA sequencing. Targeted liquid chromatography-mass spectrometry was used to examine serum central carbon-related metabolites. The correlations among metabolites, microbiotas and clinical presentations were also explored.
Although the α and β diversity between the PACG and control groups did not show a significant difference, the distribution of Blautia and Fusicatenibacter decreased significantly in the PACG group. Functional annotations of microbiota enrichment showed that the most dominant pathway was related to host metabolism. In the PACG patients, seven central carbon metabolites, namely adenosine 5'-diphosphate, dGDP, phosphoenolpyruvic acid, d-ribulose 5-phosphate, d-xylulose 5-phosphate, glucuronic acid, and malonic acid, decreased significantly, whereas two metabolites, citric acid and isocitrate, increased obviously. The mean RNFL thickness was positively correlated with phosphoenolpyruvic acid, the VF-MD was positively correlated with glucuronic acid, and the abundance of Blautia was negatively associated with citric acid.
Few species of gut microbiota were altered in the PACG patients compared to the healthy subjects. A distinct difference in the phenotype of the central carbon-related metabolites of PACG and their correlation with clinical presentations and microbiota suggests potential mechanisms of RGC impairment and novel intervention targets.
探讨原发性闭角型青光眼(PACG)患者肠道微生物群和中心碳相关代谢物的特征。
通过 16S rRNA 测序检测 30 例 PACG 患者和 30 例健康对照者的粪便微生物群。采用靶向液相色谱-质谱法检测血清中心碳相关代谢物。还探讨了代谢物、微生物群与临床表型之间的相关性。
尽管 PACG 组和对照组的α和β多样性无显著差异,但 Blautia 和 Fusicatenibacter 的分布在 PACG 组中显著下降。微生物群富集的功能注释表明,最主要的途径与宿主代谢有关。在 PACG 患者中,7 种中心碳代谢物,即腺苷 5'-二磷酸、dGDP、磷酸烯醇丙酮酸、d-核酮糖 5-磷酸、d-木酮糖 5-磷酸、葡萄糖醛酸和丙二酸,显著降低,而柠檬酸和异柠檬酸两种代谢物明显增加。平均 RNFL 厚度与磷酸烯醇丙酮酸呈正相关,VF-MD 与葡萄糖醛酸呈正相关,而 Blautia 的丰度与柠檬酸呈负相关。
与健康对照者相比,PACG 患者的肠道微生物群种类较少。PACG 患者中心碳相关代谢物表型的明显差异及其与临床表型和微生物群的相关性提示了 RGC 损伤的潜在机制和新的干预靶点。