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种植体表面在代谢综合征和 2 型糖尿病中的骨整合。

Osseointegration of implant surfaces in metabolic syndrome and type-2 diabetes mellitus.

机构信息

Biomaterials Division, NYU Dentistry, New York, New York, USA.

Department of Prosthodontics and Periodontology, Bauru School of Dentistry, University of São Paulo, Bauru, São Paulo, Brazil.

出版信息

J Biomed Mater Res B Appl Biomater. 2024 Feb;112(2):e35382. doi: 10.1002/jbm.b.35382.

Abstract

This in vivo study evaluated the bone healing response around endosteal implants with varying surface topography/chemistry in a preclinical, large transitional model induced with metabolic syndrome (MS) and type-2 diabetes mellitus (T2DM). Fifteen Göttingen minipigs were randomly distributed into two groups: (i) control (normal diet, n = 5) and (ii) O/MS (cafeteria diet for obesity induction, n = 10). Following obesity induction, five minipigs from the obese/metabolic syndrome (O/MS) group were further allocated, randomly, into the third experimental group: (iii) T2DM (cafeteria diet + streptozotocin). Implants with different surface topography/chemistry: (i) dual acid-etched (DAE) and (ii) nano-hydroxyapatite coating over the DAE surface (NANO), were placed into the right ilium of the subjects and allowed to heal for 4 weeks. Histomorphometric evaluation of bone-to-implant contact (%BIC) and bone area fraction occupancy (%BAFO) within implant threads were performed using histomicrographs. Implants with NANO surface presented significantly higher %BIC (26%) and %BAFO (35%) relative to implants with DAE surface (%BIC = 14% and %BAFO = ~28%, p < .025). Data as a function of systemic condition presented significantly higher %BIC (28%) and %BAFO (~42%) in the control group compared with the metabolically compromised groups (O/MS: %BIC = 14.35% and %BAFO = 26.24%, p < .021; T2DM: %BIC = 17.91% and %BAFO = 26.12%, p < .021) with no significant difference between O/MS and T2DM (p > .05). Statistical evaluation considering both factors demonstrated significantly higher %BIC and %BAFO for the NANO surface relative to DAE implant, independent of systemic condition (p < .05). The gain increase of %BIC and %BAFO for the NANO compared with DAE was more pronounced in O/MS and T2DM subjects. Osseointegration parameters were significantly reduced in metabolically compromised subjects compared with healthy subjects. Nanostructured hydroxyapatite-coated surfaces improved osseointegration relative to DAE, regardless of systemic condition.

摘要

本体内研究评估了在代谢综合征(MS)和 2 型糖尿病(T2DM)诱导的临床前大型过渡模型中,具有不同表面形貌/化学特性的骨内种植体的骨愈合反应。将 15 只哥廷根小型猪随机分为两组:(i)对照组(正常饮食,n=5)和(ii)O/MS 组(肥胖诱导的自助餐饮食,n=10)。肥胖诱导后,将 O/MS 组中的 5 只小型猪进一步随机分配到第三实验组:(iii)T2DM 组(自助餐饮食+链脲佐菌素)。将具有不同表面形貌/化学特性的植入物:(i)双酸蚀(DAE)和(ii)在 DAE 表面涂覆纳米羟基磷灰石(NANO),分别植入实验动物的右侧髂骨,并允许愈合 4 周。使用组织学显微镜照片对植入物螺纹内的骨-植入物接触百分比(%BIC)和骨面积占有率(%BAFO)进行组织形态计量学评估。与 DAE 表面的植入物(%BIC=14%和%BAFO=28%,p<.025)相比,具有 NANO 表面的植入物表现出更高的%BIC(26%)和%BAFO(35%)。数据作为系统条件的函数,与代谢受损组(O/MS:%BIC=14.35%和%BAFO=26.24%,p<.021;T2DM:%BIC=17.91%和%BAFO=26.12%,p<.021)相比,对照组的%BIC(28%)和%BAFO(42%)显著更高,而 O/MS 和 T2DM 之间没有显著差异(p>.05)。考虑到两个因素的统计评估表明,与 DAE 植入物相比,NANO 表面的%BIC 和%BAFO 显著更高,而与系统状态无关(p<.05)。与 DAE 相比,NANO 表面的%BIC 和%BAFO 增加幅度在 O/MS 和 T2DM 受试者中更为明显。与健康受试者相比,代谢受损受试者的骨整合参数显著降低。纳米结构羟基磷灰石涂层表面改善了骨整合,与系统状态无关。

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本文引用的文献

1
Effect of supplemental acid-etching on the early stages of osseointegration: A preclinical model.
J Mech Behav Biomed Mater. 2021 Oct;122:104682. doi: 10.1016/j.jmbbm.2021.104682. Epub 2021 Jul 13.
2
Synergistic Effects of Implant Macrogeometry and Surface Physicochemical Modifications on Osseointegration: An In Vivo Experimental Study in Sheep.
J Long Term Eff Med Implants. 2019;29(4):295-302. doi: 10.1615/JLongTermEffMedImplants.2020034194.
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Biomaterial and biomechanical considerations to prevent risks in implant therapy.
Periodontol 2000. 2019 Oct;81(1):139-151. doi: 10.1111/prd.12288.
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Effect of Obesity or Metabolic Syndrome and Diabetes on Osseointegration of Dental Implants in a Miniature Swine Model: A Pilot Study.
J Oral Maxillofac Surg. 2018 Aug;76(8):1677-1687. doi: 10.1016/j.joms.2018.02.021. Epub 2018 Mar 1.
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Obesity, Type 2 Diabetes and Bone in Adults.
Calcif Tissue Int. 2017 May;100(5):528-535. doi: 10.1007/s00223-016-0229-0. Epub 2017 Mar 9.

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