Acute‐phase response following one‐stage full‐mouth versus quadrant non‐surgical periodontal treatment in subjects with comorbid type 2 diabetes: A randomized clinical trial

医学 内科学 析因分析 剥皮和根面刨削 慢性牙周炎 牙周炎 胃肠病学 2型糖尿病 糖尿病 曼惠特尼U检验 C反应蛋白 方差分析 象限(腹部) 随机对照试验 急性期蛋白 牙科 外科 炎症 内分泌学
作者
Filippo Graziani,Stefano Gennai,Crystal Marruganti,Marina Perić,Lorenzo Ghiadoni,Urška Marhl,Morena Petrini
出处
期刊:Journal of Clinical Periodontology [Wiley]
卷期号:50 (4): 487-499 被引量:22
标识
DOI:10.1111/jcpe.13760
摘要

Abstract Aim To compare the level of inflammatory markers and endothelial function 24 h (Day 1) and 90 days (Day 90) after conventional quadrant‐wise scaling and root planing (Q‐SRP) versus one‐stage full‐mouth SRP (FM‐SRP) in patients affected by type 2 diabetes mellitus (T2DM). Materials and Methods Patients affected by periodontitis and T2DM were randomly allocated to receive FM‐SRP or Q‐SRP and followed up at Day 1 and Day 90. Serum samples, vital signs, and flow‐mediated dilation (FMD) parameters were collected at baseline, Day 1, and Day 90. Periodontal variables were collected at baseline and Day 90. The primary outcome was the C‐reactive protein (CRP) concentration at Day 1 after periodontal treatment. Student's t ‐test for independent samples was used for between‐group comparisons (Mann–Whitney U test for non‐normal data), while analysis of variance with post hoc Tukey tests (Kruskal–Wallis and Dunn tests for non‐normal data) were used for intra‐group comparisons. Results Forty subjects were included in the study. FM‐SRP produced a significant increase in CRP and a significant reduction in FMD at Day 1 compared to Q‐SRP ( p < .05). The absolute change in HbA1c (mmol/mol) from baseline to Day 90 was significantly improved in the Q‐SRP (ΔHbA1c = −1.59 [SD = 1.20]) compared to the FM‐SRP group (ΔHbA1c = −0.8 [SD = 0.95]) ( p = .04). Conclusions FM‐SRP triggers a robust acute‐phase response at 24 h after treatment compared to Q‐SRP. Such systemic acute perturbations may offset the beneficial systemic effects of periodontal treatment in terms of HbA1c reduction and improvement in endothelial function in T2DM subjects.
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