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Osteoconductive properties of upside-down bilayer collagen membranes in rat calvarial defects.
Feher, Balazs; Apaza Alccayhuaman, Karol Ali; Strauss, Franz Josef; Lee, Jung-Seok; Tangl, Stefan; Kuchler, Ulrike; Gruber, Reinhard.
Afiliación
  • Feher B; Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090, Vienna, Austria.
  • Apaza Alccayhuaman KA; Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090, Vienna, Austria.
  • Strauss FJ; Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090, Vienna, Austria.
  • Lee JS; Clinic of Reconstructive Dentistry, Center of Dental Medicine, University of Zurich, Zurich, Switzerland.
  • Tangl S; Department of Conservative Dentistry, Faculty of Dentistry, University of Chile, Santiago, Chile.
  • Kuchler U; Department of Periodontology, Research Institute for Periodontal Regeneration, College of Dentistry, Yonsei University, Seoul, Korea.
  • Gruber R; Core Facility Hard Tissue and Biomaterial Research, Karl Donath Laboratory, University Clinic of Dentistry, Medical University of Vienna, Vienna, Austria.
Int J Implant Dent ; 7(1): 50, 2021 06 07.
Article en En | MEDLINE | ID: mdl-34095987
ABSTRACT

BACKGROUND:

Bilayer collagen membranes are routinely used in guided bone/tissue regeneration to serve as osteoconductive scaffolds and prevent the invasion of soft tissues. It is recommended to place the membranes with their dense layer towards the soft tissue and their porous layer towards the bony defect area. However, evidence supporting this recommendation is lacking. This study aimed to determine whether the alignment of bilayer collagen membranes has an effect on bone regeneration.

METHODS:

In two groups of ten male Sprague-Dawley rats each, a 5-mm calvarial defect was created. Thereafter, the defect was randomly covered with a bilayer, resorbable, pure type I and III collagen membrane placed either regularly or upside-down (i.e., dense layer towards bone defect). After 4 weeks of healing, micro-computed tomography (µCT), histology, and histomorphometry of the inner cylindrical region of interest (4.5 mm in diameter) were performed to assess new bone formation and the consolidation of the collagen membrane in the defect area.

RESULTS:

Quantitative µCT showed similar bone volume (median 8.0 mm3, interquartile range 7.0-10.0 vs. 6.2 mm3, 4.3-9.4, p = 0.06) and trabecular thickness (0.21 mm, 0.19-0.23 vs. 0.18 mm, 0.17-0.20, p = 0.03) between upside-down and regular placement, both leading to an almost complete bony coverage. Histomorphometry showed comparable new bone areas between the upside-down and regularly placed membranes, 3.9 mm2 (2.7-5.4) vs. 3.8 mm2 (2.2-4.0, p = 0.31), respectively. Both treatment groups revealed the same regeneration patterns and spatial distribution of bone with and without collagen fibers, as well as residual collagen fibers.

CONCLUSIONS:

Our data support the osteoconductive properties of collagen membranes and suggest that bone regeneration is facilitated regardless of membrane layer alignment.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cráneo / Regeneración Ósea Tipo de estudio: Guideline Límite: Animals Idioma: En Revista: Int J Implant Dent Año: 2021 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cráneo / Regeneración Ósea Tipo de estudio: Guideline Límite: Animals Idioma: En Revista: Int J Implant Dent Año: 2021 Tipo del documento: Article País de afiliación: Austria