Department of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Scleroderma Unit, Azienda Ospedaliero-Universitaria Careggi (AOUC), Florence, Italy.
RMD Open. 2024 Nov 18;10(4):e004647. doi: 10.1136/rmdopen-2024-004647.
In systemic sclerosis (SSc), gastrointestinal involvement is one of the earliest events. We compared the gut microbiota (GM), its short-chain fatty acids (SCFAs) and host-derived free fatty acids (FFAs) in patients with very early diagnosis of SSc (VEDOSS) and definite SSc.
Stool samples of 26 patients with SSc, 18 patients with VEDOSS and 20 healthy controls (HC) were collected. The GM was assessed through 16S rRNA sequencing, while SCFAs and FFAs were assessed by gas chromatography-mass spectrometry.
In patients with VEDOSS, an increase in Bacteroidales and Oscillospirales orders and a decrease in Bacilli class, and genera was detected in comparison with HC. In patients with SSc, an elevated number of Acidaminococcaceae and Sutterellaceae families, along with a decrease of the Peptostreptococcaceae family and and genera was found in comparison with HC. Patients with SSc and VEDOSS had a significantly lower butyrate and higher acetate with respect to HC. In VEDOSS, an increase in Oscillospiraceae family and genus, and a decrease in class, and Lactobacillales order was identified with respect to SSc. Moreover, patients with VEDOSS exhibited higher acetate and lower valerate compared with definite SSc.
A GM dysbiosis with depletion of beneficial anti-inflammatory bacteria (especially butyrate-producing) and a significant decrease in faecal butyrate was identified in patients with VEDOSS. This early GM imbalance may foster the growth of inflammatory microbes, worsening intestinal dysbiosis and inflammation in early SSc stages. The potential butyrate administration in early disease phases might be considered as a novel therapeutic approach to mitigate gastrointestinal discomfort and progression preserving patient's quality of life.
在系统性硬化症(SSc)中,胃肠道受累是最早发生的事件之一。我们比较了早期诊断的系统性硬化症(VEDOSS)和明确诊断的系统性硬化症患者的肠道微生物群(GM)、其短链脂肪酸(SCFAs)和宿主来源的游离脂肪酸(FFAs)。
收集了 26 例 SSc 患者、18 例 VEDOSS 患者和 20 例健康对照(HC)的粪便样本。通过 16S rRNA 测序评估 GM,通过气相色谱-质谱法评估 SCFAs 和 FFAs。
与 HC 相比,VEDOSS 患者的拟杆菌目和波动螺旋菌目增加,芽孢杆菌纲和属减少。与 HC 相比,SSc 患者的氨基酸球菌科和萨特氏菌科家族数量增加,而消化链球菌科家族和属数量减少。与 HC 相比,SSc 和 VEDOSS 患者的丁酸减少,乙酸增加。在 VEDOSS 中,与 SSc 相比,发现振荡螺旋菌科家族和属增加,梭菌纲和乳杆菌目减少。此外,与明确的 SSc 相比,VEDOSS 患者的乙酸增加,戊酸减少。
VEDOSS 患者存在 GM 失调,有益的抗炎细菌(尤其是产生丁酸的细菌)减少,粪便丁酸显著减少。这种早期 GM 失衡可能会促进炎症微生物的生长,加重早期 SSc 阶段的肠道菌群失调和炎症。在疾病早期阶段,可能考虑使用潜在的丁酸盐作为一种新的治疗方法,以减轻胃肠道不适和疾病进展,保持患者的生活质量。