阿尔茨海默病中牙龈卟啉菌阿加明脱氨酶的表达失调

Asma Hamdi, Sana Baroudi, Alya Gharbi, Wafa Babay, Ahmed Baligh Laaribi, Imene Kacem, Saloua Mrabet, Ines Zidi, Naouel Klibi, Riadh Gouider, Hadda-Imene Ouzari
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引用次数: 0

摘要

背景:阿尔茨海默病(AD)是最普遍的神经退行性疾病,对全球健康造成了重大负担。阿尔茨海默病的特点是认知能力逐渐下降和记忆力减退。新近的研究表明,牙周炎,特别是牙龈卟啉单胞菌(P. gingivalis)等口腔细菌的存在与老年痴呆症的进展之间存在潜在联系。牙龈卟啉单胞菌会产生一种酶,即阿格马丁脱氨酶(AgD),它能将阿格马丁转化为 N-氨基甲酰基腐胺(NCP),作为必需多胺的前体。最近的研究证实了多胺代谢紊乱与认知障碍之间的相关性:本研究旨在探讨在注意力缺失症的背景下牙龈脓疱菌阿加明脱氨酶(PgAgD)的失调情况:方法:共收集了 54 人的唾液样本,其中包括 27 名 AD 患者和 27 名健康对照者。方法:共采集了54人的唾液样本,其中包括27名AD患者和27名健康对照者,采用Real-Time PCR定量分析PgAgD基因的表达:结果表明,与健康对照组相比,AD 患者唾液样本中 PgAgD 基因的表达明显下降。牙周炎晚期的 AD 患者也出现了这种基因表达下调的情况。此外,还观察到 PgAgD 表达的下降与 30 项迷你精神状态检查(MMSE)评分之间存在相关性:这些研究结果表明,测量唾液中 PgAgD 的表达可作为一种非侵入性工具,用于监测 AD 的进展,并有助于牙周炎患者的早期诊断。还需要进一步的研究来验证我们的结果,并探索牙周炎、PgAgD表达和AD病理生理学之间的内在联系。
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Dysregulation of Porphyromonas gingivalis Agmatine Deiminase Expression in Alzheimer's Disease.

Background: Alzheimer's disease (AD) is the most prevalent neurodegenerative disorder, with a significant burden on global health. AD is characterized by a progressive cognitive decline and memory loss. Emerging research suggests a potential link between periodontitis, specifically the presence of oral bacteria such as Porphyromonas gingivalis (P. gingivalis), and AD progression. P. gingivalis produces an enzyme, Agmatine deiminase (AgD), which converts agmatine to N-carbamoyl putrescine (NCP), serving as a precursor to essential polyamines. Recent studies have confirmed the correlation between disruptions in polyamine metabolism and cognitive impairment.

Objective: This study aims to investigate the dysregulation of P. gingivalis Agmatine deiminase (PgAgD) in the context of AD.

Methods: Saliva samples were collected from a total of 54 individuals, including 27 AD patients and 27 healthy controls. The expression of the PgAgD gene was analyzed using quantitative Real-- Time PCR.

Results: The results showed a significant decrease in PgAgD gene expression in the saliva samples of AD patients compared to healthy controls. This downregulation was found in AD patients with advanced stages of periodontitis. Additionally, a correlation was observed between the decrease in PgAgD expression and the 30-item Mini-Mental State Examination (MMSE) score.

Conclusion: These findings suggest that measuring PgAgD expression in saliva could be a noninvasive tool for monitoring AD progression and aid in the early diagnosis of patients with periodontitis. Further research is needed to validate our results and explore the underlying mechanisms linking periodontitis, PgAgD expression, and AD pathophysiology.

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