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Ditemukan 3 dokumen yang sesuai dengan query
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Stefani Dewi Widyawati
"Latar Belakang: PRF adalah trombosit generasi kedua yang digunakan untuk mempercepat penyembuhan jaringan lunak dan keras dan merupakan matriks fibrin alami yang mengandung platelet dan leukosit sitokin. Pemberian growth Factor yang cukup lama (TGF β1) dari penambahan PRF pada DPBB dapat mengakibatkan peningkatan regenerasi tulang dibandingkan dengan pemberian DPBB saja. Tujuan: mengevaluasi pengaruh platelet rich fibrin dalam meningkatkan regenerasi tulang yang dilihat melalui konsentrasi TGF β1 dan osteocalcin. Metode: autologous PRF dibuat dengan menggunakan 10 ml darah yang dikumpulkan dari regio antecubital dari relawan. Sampel darah diperlakukan sesuai dengan protokol PRF (Dohan et all.2006). Bekuan fibrin di tengah tabung digunakan sebagai tambahan untuk bahan bone graft (DPBB). Kelompok-kelompok ini sampel PRF diinkubasi pada suhu 370C dan 5% CO2 selama 1 hari, 5 hari dan 7 hari. Semua sampel dipanen pada waktu yang tepat dan disimpan lalu diperiksa Enzyme-Linked Immunosorbent Assay (ELISA) analisis untuk TGF β1 tingkat dan tingkat ostecalcin. Hasil: terdapat perbedaan bermakna dari PRF + DPBB dibandingkan dengan DPBB di hari 1, dari PRF dibandingkan dengan kontrol pada hari 5, dari PRF + DPBB dibandingkan dengan kontrol pada hari ke 7, dan dari DPBB dibandingkan dengan kontrol pada hari ke 7 (p <. 05). Terdapat perbedaan bermakna dari PRF + DPBB dibandingkan dengan kontrol pada hari ke 1,5 dan 7, dari DPBB dibandingkan dengan kontrol pada hari 1,5, dan 7, dan dari PRF membandingkan toPRF + DPBB dan DPBB (p <.05). Kesimpulan: Penambahan PRF atau PRF + DPBB dalam kultur osteoblas dapat meningkatkan konsentrasi TGF β1 dan osteokalsin, yang dimulai 1 hari ke hari 7

Background: PRF is a second generation platelet used to accelerate soft and hard tissue healing and is a strictctly autologous fibrin matrix containing a large quantitiy of platelet and leukocyte cytokines. Given prolonged growth factor (TGF β1) from PRF treatment in DPBB might result in increasing bone regeneration compare to those treated with DPBB. Purpose: evaluate the influence of platelet rich fibrin in enhancing natural bone regeneration through the levels of TGF β1 and osteocalcin. Method: Autologous PRF was prepared by using 10 ml of autologous whole blood collected from the antecubital regio of a volunteers. Blood samples were treated according to the PRF protocol (Dohan et all.2006). A fibrin clot in the middle of tube was used as an adjunct to grafting material (DPBB). These groups of PRF samples were incubated at 370C and 5%CO2 for 1 day, 5 days and 7 days. All sample were harvested at the appropriate time and and stored for later Enzyme-Linked ImmunoSorbent Assay (ELISA) analysis for TGF β1 level and osteocalcin level. Result: There are significantly differents from PRF+DPBB compare to DPBB at day 1, from PRF compare to control at days 5, from PRF+DPBB compare to control at day 7, and from DPBB compare to control at days 7 (p<.05). There are significantly differents from PRF+DPBB compare to control at day 1,5 and 7, from DPBB compare to control at days 1,5,and 7, and from PRF compare toPRF+DPBB and DPBB (p<.05). Conclusion: Addition PRF or PRF + DPBB in cultured osteoblasts can increase the concentration of TGF β1 and osteocalcin, which began 1 day to day 7"
Fakultas Kedokteran Gigi Universitas Indonesia, 2014
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UI - Tugas Akhir  Universitas Indonesia Library
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Paramita Pandansari
"[ABSTRAK
Latar Belakang: Penggunaan biomaterial berupa bahan tandur tulang dan membran untuk prosedur Guided Bone Regeneration (GBR) sangat diperlukan di bidang bedah maksilofasial dan, untuk mengatasi defek tulang yang dapat terjadi oleh berbagai sebab. Penelitian ini bertujuan untuk mengetahui efek pemakaian bahan tandur tulang DFDBX dengan membran perikardium (MPK) bovine pada defek tulang kalvaria tikus.
Bahan dan Metode: Studi eksperimental ini menggunakan 45 ekor tikus Sprague Dawley sebagai hewan coba dibagi dalam 3 kelompok secara acak. Ciritical size defect sebesar diameter 5 mm dibuat pada tulang kalvaria seluruh hewan coba. Kelompok I merupakan kelompok kontrol, tidak diberikan perlakuan dan defek dibiarkan sembuh dengan sendirinya, kelompok II yang diberi DFDBX, dan pada kelompok III defek diisi dengan DFDBX dan ditutup dengan MPK (DFDBX+MPK). Setelah 1,4 dan 8 minggu dilakukan dilakukan pengorbanan pada kelompok hewan coba, dilanjutkan dengan evaluasi secara radiologik, histopatologik untuk reaksi radang, pertumbuhan tulang dan pemeriksaan imunohistokimia dengan osteokalsin. Data dianalisis secara statistik dengan menggunakan uji ANOVA.
Hasil: Penilaian radiografik diperoleh perbedaan bermakna pada rerata densitas area defek minggu ke 8 antara kelompok kontrol dengan DFDBX+MPK (p<0,001) dan antara kelompok DFDBX dengan DFDBX+MPK (p=0,03).
Pertumbuhan tulang baru pada minggu ke 8 tertinggi adalah pada kelompok DFDBX+MPK dengan perbedaan bermakna dengan kelompok kontrol (p=0,016) dan dengan kelompok DFDBX nilai p=0,048. Ekspresi osteokalsin minggu ke-8 menunjukkan perbedaan bermakna antara kelompok kontrol dengan kelompok DFDBX (p<0,001) maupun dengan kelompok DFDBX+MPK (p=0,0013), namun tidak terdapat perbedaan bermakna antara kelompok DFDBX dengan kelompok MPK (p=1,000).
Kesimpulan: Penggunaan DFDBX dengan kombinasi MPK terbukti secara radiologik, histopatologik dan imunohistokimia dapat meningkatkan regenerasi tulang pada defek tulang kalvaria.

ABSTRACT
Background: Reconstruction of cranial and maxillofacial defects is a challenging task. The standard method has included bone grafting and using membrane in guided bone regeneration procedure. Using biomaterial such as bone grafting and membrane for Guided Bone Regeneration (GBR) procedures is an essential issue in maxillofacial and dental reconstruction surgery to overcome bone defects caused by various etiologies. Our study was aimed to identify the effect of using Demineralized Freeze-Dried Bone Xenograft (DFDBX) with (or without) bovine pericardium membrane (PCM) on the treatment of rats calvarial bone defects.
Materials and Method: The experimental study used 45 Sprague-Dawley rats as the experimental animals, which were categorized randomly into three groups, i.e. the control group, DFDBX group, and DFDBX+PCM group. The 5-mm-critical-sized calvarial defects were created in all experimental animals. The first group was a control group, which did not receive any treatment with self-limiting defects; while subjects in the second group received DFDBX (DFDBX group) and in the third group, the defects were filled with DFDBX and PCM (DFDBX + PCM group). Animals were sacrified at the 1st, 4th, and 8th weeks following the surgery. Subsequently, an evaluation was carried out using radiological analysis, histopathological assay to observe inflammatory reaction and bone growth, as well as immunohistochemical analysis of osteocalcin. Data were analyzed statistically using ANOVA test. The specimens were embedded ini paraffin, serially cut, and stained with hematoxylin and eosin for analysis under light microscope. The inflammation reaction, new bone formation, and the rest of DFDBX and PCM were histomorphometrically evaluated. Immunohistochemical analysis of osteocalcin expression was performed.
Results: Radiological analysis demonstrated a significant difference of mean bone density in the defect area at the 8th week between subjects in the control group and those in DFDBX+PCM group (p < 0.001), as well as between subjects in the DFDBX group and those in DFDBX+PCM group (p = 0.03). The highest rate of bone healing at the 8th week was found in DFDBX+PCM group, which showed significant difference compared to the control group (p=0.016) and to DFDBX group (p=0.048). There was a significant difference of osteocalcin expression between the control group and DFDBX group (p < 0.001), as well as between the control group and DFDBX + PCM group (p=0,0013). However, there was no significant difference between the DFDBX group and the DFDBX+PCM group (p = 1.000).
Conclusion: Our radiological, histopahtological and immunohistochemical evaluation has demonstrated that DFDBX combined with PCM increases bone regeneration in the treatment of bone calvarial defect. ;Background :Reconstruction of cranial and maxillofacial defects is a challenging task.
The standard method has been bone grafting and using membrane in guided bone
regeneration procedure.
The aim of this study was to analyze the effect of Demineralized Freeze Dried Bone
Xenograft (DFDBX) with (or without)bovine pericardium membrane (PCM) on bone
regeneration, in surgically created critical-size defects in rat calvaria, radiographically,
histopathologically and immunohistochemically.
Material and Methods :Surgical critical-size bone defects were created in 45 animals
that randomly divided into three groups : control group, DFDBX group, and
DFDBX+PCM group. Animals were sacrified at 1, 4 and 8 weeks post surgery.
Radiological analysis was done. The specimens were embedded ini paraffin, serially cut,
and stained with hematoxylin and eosin for analysis under light microscope. The
inflammation reaction, new bone formation, and the rest of DFDBX and PCM were
histomorphometrically evaluated. Immunohistochemical analysis of osteocalcin
expression was performed.
Result : DFDBX and DFDBX+PCM groups demonstrated superior bone healing
compared with control group. Group DFDBX+PCM showmore advanced healing at 8
weeks post surgery and show the highest density radiographically as compared with the
other group DFDBX and control.Immunohistochemistry revealed the presence of
osteocalcin in osteoblast and matrix extracellular and show significant differences were
noted between DFDBX and DFDBX+PCM to control groups.
Conclusion : Application of DFDBX combined with bovine PCM gave the best result in bone regeneration of critical size defects in rat calvaria. , Background :Reconstruction of cranial and maxillofacial defects is a challenging task.
The standard method has been bone grafting and using membrane in guided bone
regeneration procedure.
The aim of this study was to analyze the effect of Demineralized Freeze Dried Bone
Xenograft (DFDBX) with (or without)bovine pericardium membrane (PCM) on bone
regeneration, in surgically created critical-size defects in rat calvaria, radiographically,
histopathologically and immunohistochemically.
Material and Methods :Surgical critical-size bone defects were created in 45 animals
that randomly divided into three groups : control group, DFDBX group, and
DFDBX+PCM group. Animals were sacrified at 1, 4 and 8 weeks post surgery.
Radiological analysis was done. The specimens were embedded ini paraffin, serially cut,
and stained with hematoxylin and eosin for analysis under light microscope. The
inflammation reaction, new bone formation, and the rest of DFDBX and PCM were
histomorphometrically evaluated. Immunohistochemical analysis of osteocalcin
expression was performed.
Result : DFDBX and DFDBX+PCM groups demonstrated superior bone healing
compared with control group. Group DFDBX+PCM showmore advanced healing at 8
weeks post surgery and show the highest density radiographically as compared with the
other group DFDBX and control.Immunohistochemistry revealed the presence of
osteocalcin in osteoblast and matrix extracellular and show significant differences were
noted between DFDBX and DFDBX+PCM to control groups.
Conclusion : Application of DFDBX combined with bovine PCM gave the best result in bone regeneration of critical size defects in rat calvaria. ]"
Fakultas Kedokteran Universitas Indonesia, 2015
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UI - Tugas Akhir  Universitas Indonesia Library
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RR. Tut Wuri Andajani
"Gen Osteokalsin merupakan gen kandidat terjadinya osteoporosis.. Polimorfisme pada gen tersebut menyebabkan densitas tulang menurun. Densitas tulang juga dipengaruhi oleh aktivitas fisik dan asupan makanan. Faktor-faktor tersebut untuk mendapatkan model prediksi tulang sehingga dapat dilakukan pencegahan. Dengan demikian dilakukan pengukuran densitas tulang, pemeriksaan biokimia darah serta polimorfisme gen osteokalsin digunakan enzim HindIII dengan teknik PCR-RFLP. Diperoleh rataan usia 67,21±9,1; IMT 22,14±4,08; fosfat alkalin 87,26±25; kalsium 8,9±0,82; estradiol 24,8±11,7; osteokalsin 1,75±0,83; mempunyai T-score ≤ - 2,5 dengan varian TT (64,3%) diikuti varian CC (60,6%) dan CT (50%) sehingga diperoleh model yang dapat memprediksi derajat keparahan tulang.

The aim of the research to obtain a model that uses the genetic factors, the environment and nutrient to predict bone density and risk of osteoporotic fracture. Bone mineral density and biochemical markers were determined, as well as the C298T polymorphism status of osteocalcin gene using PCR-RFLP. The subjects had a mean age of 67.2±9.1 years. ; BMD 22.14±4.08; phosphate alkaline 87.26±25; calcium 8.9 ±0.82; estradiol 24.8±11.7; osteocalcin 1.75±0.83; the C298T polymorphic genotypes showed TT (64.3%) CC (60.6 %) and a CT (50%) determine in T-score≤ -2,5. We identified a model of age and the level osteocalcin that can predict severity of bone density."
Jakarta: Fakultas Kedokteran Gigi Universitas Indonesia, 2014
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UI - Disertasi Membership  Universitas Indonesia Library