Evaluation of Salivary Opiorphin Levels in Acute Pericoronitis Related Pain.

IF 0.7 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Nigerian Journal of Clinical Practice Pub Date : 2025-03-01 Epub Date: 2025-04-11 DOI:10.4103/njcp.njcp_445_24
S Y Ertem, M S Ozdogan
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引用次数: 0

Abstract

Background: Opiorphin is a peptide that can exhibit varying concentrations in saliva in relation to pain and may serve as a potential pain biomarker.

Aim: This study aimed to evaluate pain-related changes in salivary opiorphin levels in patients with acute pericoronitis.

Materials and methods: A total of 40 saliva samples were analyzed by taking two different samples from 20 patients. Non-stimulated saliva samples were collected using uncovered cotton rolls from the same patients during tooth extraction, when acute pain was present due to acute pericoronitis, and again 1 week post-extraction, after the pain had subsided. Patients' pain levels were assessed before treatment and at a 7-day follow-up visit using a visual analog scale just before saliva sampling. Opiorphin levels in the presence and absence of pain were measured using a human opiorphin ELISA kit (Hangzhou Eastbiopharm Co., Ltd., Hangzhou, China). Statistical analyses were conducted using International Business Machines (IBM) Statistical Package for the Social Sciences (SPSS) Statistics Version 25 (IBM SPSS, Chicago, IL). The opiorphin levels in samples taken from saliva before and after tooth extraction were evaluated using Analysis of Variance (ANOVA).

Results: Mean salivary opiorphin levels were found to differ significantly between the presence of pain due to acute pericoronitis and the pain-free period following treatment. Salivary opiorphin concentration was significantly higher before treatment (17.38 ng/ml ± 5.83 ng/ml) compared to after treatment (13.54 ng/ml ± 5.37 ng/ml). The findings of this study suggest that pain due to acute pericoronitis causes a statistically significant increase in salivary opiorphin levels (P = 0.026). Saliva samples from healthy patients with acute pericoronitis were collected at the same time of day to minimize environmental variables. The age and gender of the participants did not affect opiorphin levels before or after treatment.

Conclusion: The findings of this study suggest that salivary opiorphin levels increase in the presence of pain associated with acute pericoronitis. Future studies with larger sample sizes conducted across different populations may further contribute to understanding opiorphin as a potential pain mediator.

急性冠周炎相关疼痛患者唾液Opiorphin水平的评价。
背景:Opiorphin是一种肽,在唾液中表现出与疼痛相关的不同浓度,可能作为一种潜在的疼痛生物标志物。目的:本研究旨在评估急性冠周炎患者唾液opiorphin水平的疼痛相关变化。材料与方法:选取20例患者的两份不同的唾液样本,共40份唾液样本进行分析。在拔牙期间,当急性冠周炎引起急性疼痛时,使用未盖的棉卷收集同一患者的非刺激唾液样本,并在拔牙后1周疼痛消退后再次收集唾液样本。在治疗前和7天的随访中,在唾液取样前使用视觉模拟量表评估患者的疼痛水平。使用人Opiorphin ELISA试剂盒(Hangzhou Eastbiopharm Co., Ltd, Hangzhou, China)检测疼痛存在和不存在时的Opiorphin水平。使用国际商业机器(IBM)社会科学统计软件包(SPSS)统计版本25 (IBM SPSS,芝加哥,伊利诺伊州)进行统计分析。采用方差分析(ANOVA)对拔牙前后唾液样本中的opiorphin水平进行评估。结果:在急性冠周炎引起疼痛和治疗后无痛期间,平均唾液opiorphin水平有显著差异。治疗前唾液opiorphin浓度(17.38 ng/ml±5.83 ng/ml)显著高于治疗后(13.54 ng/ml±5.37 ng/ml)。本研究结果表明,急性冠周炎引起的疼痛导致唾液opiorphin水平升高,具有统计学意义(P = 0.026)。在一天的同一时间收集健康急性冠周炎患者的唾液样本,以尽量减少环境变量。参与者的年龄和性别对治疗前后的opiorphin水平没有影响。结论:本研究结果表明,急性冠周炎患者出现疼痛时,唾液opiorphin水平升高。未来在不同人群中进行的更大样本量的研究可能进一步有助于理解opiorphin作为潜在的疼痛介质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nigerian Journal of Clinical Practice
Nigerian Journal of Clinical Practice MEDICINE, GENERAL & INTERNAL-
CiteScore
1.40
自引率
0.00%
发文量
275
审稿时长
4-8 weeks
期刊介绍: The Nigerian Journal of Clinical Practice is a Monthly peer-reviewed international journal published by the Medical and Dental Consultants’ Association of Nigeria. The journal’s full text is available online at www.njcponline.com. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles on any OAI-compliant institutional / subject-based repository. The journal makes a token charge for submission, processing and publication of manuscripts including color reproduction of photographs.
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