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Dental Pulp Mesenchymal Stem Cells as a Treatment for Periodontal Disease in Older Adults

机译:牙科纸浆间充质干细胞作为老年人牙周病的治疗方法

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Periodontal disease (PD) is one of the main causes of tooth loss and is related to oxidative stress and chronic inflammation. Although different treatments have been proposed in the past, the vast majority do not regenerate lost tissues. In this sense, the use of dental pulp mesenchymal stem cells (DPMSCs) seems to be an alternative for the regeneration of periodontal bone tissue. A quasi-experimental study was conducted in a sample of 22 adults between 55 and 64 years of age with PD, without uncontrolled systemic chronic diseases. Two groups were formed randomly: (i) experimental group (EG) n=11, with a treatment based on DPMSCs; and a (ii) control group (CG) n=11, without a treatment of DPMSCs. Every participant underwent clinical and radiological evaluations and measurement of bone mineral density (BMD) by tomography. Saliva samples were taken as well, to determine the total concentration of antioxidants, superoxide dismutase (SOD), lipoperoxides, and interleukins (IL), before and 6 months after treatment. All subjects underwent curettage and periodontal surgery, the EG had a collagen scaffold treated with DPMSCs, while the CG only had the collagen scaffold placed. The EG with DPMSCs showed an increase in the BMD of the alveolar bone with a borderline statistical significance (baseline 638.82±181.7 vs. posttreatment 781.26±162.2 HU, p=0.09). Regarding oxidative stress and inflammation markers, salivary SOD levels were significantly higher in EG (baseline 1.49±0.96 vs. 2.14±1.12?U/L posttreatment, p0.05) meanwhile IL1β levels had a decrease (baseline 1001.91±675.5vs. posttreatment 722.3±349.4?pg/ml, p0.05). Our findings suggest that a DPMSCs treatment based on DPMSCs has both an effect on bone regeneration linked to an increased SOD and decreased levels of IL1β in aging subjects with PD.
机译:牙周病(PD)是牙齿损失的主要原因之一,与氧化应激和慢性炎症有关。虽然过去已经提出了不同的治疗,但绝大多数不会再生丢失的组织。从这个意义上讲,使用牙髓间充质干细胞(DPMSCs)似乎是牙周骨组织再生的替代方案。在55至64岁的成人的样品中进行了准实验研究,PD,没有不受控制的全身慢性疾病。随机形成两组:(i)实验组(例如)n = 11,基于DPMSC的治疗;和(II)对照组(CG)n = 11,没有DPMSCs的治疗。每个参与者通过断层扫描接受临床和放射性评估和骨密度(BMD)的测量。同样考虑了唾液样品,以确定治疗后6个月和6个月的抗氧化剂,超氧化物歧化酶(SOD),脂过氧化物和白细胞介素(IL)的总浓度。所有受试者都接受了刮曲线和牙周手术,例如用DPMSC处理胶原蛋白支架,而CG仅放置胶原蛋白支架。例如,具有DPMSCs的肺泡骨BMD增加,具有边缘线统计学意义(基线638.82±181.7与后处理781.26±162.2胡,P = 0.09)。关于氧化应激和炎症标记,唾液草皮水平均显着更高(基线1.49±0.96 vs.214±1.12?U / L后疗法,P <0.05)同时IL1β水平降低(基线1001.91±675.5Vs。后处理722.3 ±349.4?pg / ml,p <0.05)。我们的研究结果表明,基于DPMSCs的DPMSCs治疗对骨再生的效果有关与PD的老化受试者中的SOD和IL1β水平增加的骨再生。

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