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第六届世界口腔医学研讨会:药物性唾液腺功能障碍的系统评价

World Workshop on Oral Medicine VI: a systematic review of medication-induced salivary gland dysfunction.

作者信息

Villa A, Wolff A, Narayana N, Dawes C, Aframian D J, Lynge Pedersen A M, Vissink A, Aliko A, Sia Y W, Joshi R K, McGowan R, Jensen S B, Kerr A R, Ekström J, Proctor G

机构信息

Division of Oral Medicine and Dentistry, Brigham and Women's Hospital, Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.

Tel-Aviv Sourasky Medical Center and Saliwell Ltd., Harutzim, Israel.

出版信息

Oral Dis. 2016 Jul;22(5):365-82. doi: 10.1111/odi.12402. Epub 2016 Jan 20.

Abstract

The aim of this paper was to perform a systematic review of the pathogenesis of medication-induced salivary gland dysfunction (MISGD). Review of the identified papers was based on the standards regarding the methodology for systematic reviews set forth by the World Workshop on Oral Medicine IV and the PRISMA statement. Eligible papers were assessed for both the degree and strength of relevance to the pathogenesis of MISGD as well as on the appropriateness of the study design and sample size. A total of 99 papers were retained for the final analysis. MISGD in human studies was generally reported as xerostomia (the sensation of oral dryness) without measurements of salivary secretion rate. Medications may act on the central nervous system (CNS) and/or at the neuroglandular junction on muscarinic, α-and β-adrenergic receptors and certain peptidergic receptors. The types of medications that were most commonly implicated for inducing salivary gland dysfunction were those acting on the nervous, cardiovascular, genitourinary, musculoskeletal, respiratory, and alimentary systems. Although many medications may affect the salivary flow rate and composition, most of the studies considered only xerostomia. Thus, further human studies are necessary to improve our understanding of the association between MISGD and the underlying pathophysiology.

摘要

本文旨在对药物性涎腺功能障碍(MISGD)的发病机制进行系统评价。根据第四届口腔医学世界研讨会制定的系统评价方法标准和PRISMA声明,对已识别的论文进行了综述。对符合条件的论文进行评估,看其与MISGD发病机制的相关程度和强度,以及研究设计和样本量的合理性。最终分析共保留了99篇论文。人体研究中的MISGD通常被报告为口干症(口腔干燥的感觉),而未测量唾液分泌率。药物可能作用于中枢神经系统(CNS)和/或神经腺体连接处的毒蕈碱、α和β肾上腺素能受体以及某些肽能受体。最常被认为会导致涎腺功能障碍的药物类型是作用于神经、心血管、泌尿生殖、肌肉骨骼、呼吸和消化系统的药物。尽管许多药物可能会影响唾液流速和成分,但大多数研究仅考虑了口干症。因此,有必要进行进一步的人体研究,以增进我们对MISGD与潜在病理生理学之间关联的理解。

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