Combination of leukocyte and platelet-rich fibrin and demineralized bovine bone graft enhanced bone formation and healing after maxillary sinus augmentation: a randomized clinical trial

被引:20
作者
de Almeida Malzoni, Carolina Mendonca [1 ]
Pichotano, Elton Carlos [1 ]
de Paula, Luiz Guilherme Freitas [1 ]
de Souza, Ricardo Violante [2 ]
Okamoto, Roberta [3 ]
Austin, Rupert S. [4 ]
Marcantonio, Elcio, Jr. [1 ]
de Molon, Rafael Scaf [5 ]
Zandim-Barcelos, Daniela Leal [1 ]
机构
[1] UNESP, Sao Paulo State Univ, Sch Dent Araraquara, Dept Diag & Surg, Rua Humaita 1680, BR-14801903 Araraquara, SP, Brazil
[2] Univ Sao Paulo, Sao Paulo Univ, Sch Med Ribeirao Preto, BR-14040904 Ribeirao Preto, SP, Brazil
[3] UNESP, Sao Paulo State Univ, Sch Dent Aracatuba, Dept Basic Sci, BR-16015050 Aracatuba, SP, Brazil
[4] Guys Hosp, Kings Coll London, Tissue Engn & Biophoton, Dent Inst, London, England
[5] UNESP, Sao Paulo State Univ, Sch Dent Aracatuba, Dept Diag & Surg, Rua Jose Bonifacio,1193 Vila Mendonca, BR-16015050 Aracatuba, SP, Brazil
关键词
Platelet-rich fibrin; Sinus floor augmentation; Dental implants; Demineralized bovine bone; Bone graft; FLOOR AUGMENTATION; IMPLANT STABILITY; MEMBRANE ELEVATION; AUTOGENOUS BONE; PLASMA; PLACEMENT; DEFECTS; PART;
D O I
10.1007/s00784-023-05167-z
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and objectiveThe resorption of alveolar ridge bone and maxillary sinus pneumatization are challenges to implant-supported prosthetic rehabilitation. Bone regeneration using bone substitutes and growth factors are alternatives for maxillary sinus augmentation (MSA). Therefore, we sought to evaluate the effects of the association between leukocyte and platelet-rich fibrin (L-PRF) and deproteinized bovine bone mineral (DBBM) in MSA procedures.Materials and methodsThirty-six maxillary sinuses from 24 individuals were included in this randomized clinical trial. The maxillary sinuses were randomly grafted with LPRF and DBBM (test group) or grafted only with DBBM (positive control). Dental implants were installed in the test group following two periods of evaluation: after 4 (DBBM+LPRF4) and 8 (DBBM+LPFR8) months of sinus graft healing, while the control group received implants only after 8 months. Cone beam computed tomography (CBCT) was taken 1 week after surgery (T1) and before implant placement (T2). Bone samples were collected during implant placement for histomorphometric and immunohistochemical (IHC) analysis. The primary implant stability was assessed by resonance frequency analysis.ResultsCBCT analysis demonstrated a significant decrease in bone volume from T1 to T2 in all groups without differences among them. Histologically, the test group showed significantly increase in bone neoformation in both periods of evaluation (LPRF+DBBM4: 44.70 & PLUSMN;14.01%; LPRF+DBBM8: 46.56 & PLUSMN;12.25%) compared to the control group (32.34 & PLUSMN;9.49%). The control group showed the highest percentage of residual graft. IHC analysis showed increased staining intensity of osteocalcin (OCN), vascular endothelial growth factor (VEGF), and runt related transcription factor 2 (RUNX-2) in LPRF+DBBM4 group, and osteopontin (OPN) in the L-PRF+DBBM8. Primary implant stability was successfully achieved (above 60 in implant stability quotient) in all the evaluated groups.ConclusionCombination of L-PRF and DBBM increased and accelerated new bone formation allowing early implant placement probably due to the higher protein expression of RUNX2, VEGF, OCN, and OPN. These data suggest that the use of L-PRF might be an interesting alternative to use in combination with DBBM for augment the maxillary sinuses allowing the installation of appropriate length implants in shorter period of time.Trial registrationThis study was registered before participant recruitment in Brazilian Registry of Clinical Trials (ReBEC - RBR-95m73t).
引用
收藏
页码:5485 / 5498
页数:14
相关论文
共 44 条
[1]  
Anitua E, 1999, INT J ORAL MAX IMPL, V14, P529
[2]  
BOYNE PJ, 1980, J ORAL SURG, V38, P613
[3]   A literature review on biomaterials in sinus augmentation procedures [J].
Browaeys, Hilde ;
Bouvry, Peter ;
De Bruyn, Hugo .
CLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH, 2007, 9 (03) :166-177
[4]   Regenerative potential of leucocyte- and platelet-rich fibrin. Part A: intra-bony defects, furcation defects and periodontal plastic surgery. A systematic review and meta-analysis [J].
Castro, Ana B. ;
Meschi, Nastaran ;
Temmerman, Andy ;
Pinto, Nelson ;
Lambrechts, Paul ;
Teughels, Wim ;
Quirynen, Marc .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2017, 44 (01) :67-82
[5]   Platelet-rich fibrin (PRF): A second-generation platelet concentrate. Part V: Histologic evaluations of PRF effects on bone allograft maturation in sinus lift [J].
Choukroun, J ;
Diss, A ;
Simonpieri, A ;
Girard, MO ;
Schoeffler, C ;
Dohan, SL ;
Dohan, AJJ ;
Mouhyi, J ;
Dohan, DM .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 2006, 101 (03) :299-303
[6]   A randomized clinical trial evaluating maxillary sinus augmentation with different particle sizes of demineralized bovine bone mineral: histological and immunohistochemical analysis [J].
de Molon, R. S. ;
Magalhaes-Tunes, F. S. ;
Semedo, C. V. ;
Furlan, R. G. ;
de Souza, L. G. L. ;
de Souza Faloni, A. P. ;
Marcantonio, E., Jr. ;
Faeda, R. S. .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2019, 48 (06) :810-823
[7]  
Molon Rafael Scaf de, 2015, Braz. Dent. J., V26, P11, DOI 10.1590/0103-6440201300290
[8]   Primary Stability Determination by Means of Insertion Torque and RFA in a Sample of 4,135 Implants [J].
Degidi, Marco ;
Daprile, Giuseppe ;
Piattelli, Adriano .
CLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH, 2012, 14 (04) :501-507
[9]   Improvement of bone repair with l-PRF and bovine bone in calvaria of rats. histometric and immunohistochemical study [J].
do Lago, Eliel Scarpioni ;
Ferreira, Sabrina ;
Garcia Jr, Idelmo Rangel ;
Okamoto, Roberta ;
Mariano, Ronaldo Celio .
CLINICAL ORAL INVESTIGATIONS, 2020, 24 (05) :1637-1650
[10]  
Dohan David M, 2006, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, V101, pe51, DOI 10.1016/j.tripleo.2005.07.010