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Ditemukan 4 dokumen yang sesuai dengan query
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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
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Dimas Ilham Hutomo
"Latar Belakang: Osteoporosis merupakan penyakit yang ditandai oleh penurunan massa tulang, sehingga menyebabkan perubahan mikroarsitektur tulang. Osteokalsin adalah protein penanda adanya pembentukan dan resorpsi tulang. Tujuan: Menganalisis hubungan antara kadar osteokalsin dengan status periodontal pada perempuan berisiko osteoporosis. Metode: Studi potong lintang pada 70 perempuan pascamenopause. Dilakukan pemeriksaan status periodontal dan kadar osteokalsin dalam serum menggunakan metode ELISA. Hasil: Tidak terdapat perbedaan kadar osteokalsin antara subjek osteoporosis, osteopenia, dan normal. Terdapat hubungan antara kadar osteokalsin terhadap kehilangan perlekatan klinis pada subjek osteoporosis. Kesimpulan: Ada hubungan antara kadar osteokalsin dengan status periodontal pada subjek osteoporosis.

Background: Osteoporosis is defined as a bone disease characterised by a decrease in bone mass results in bone microarchitecture alteration. Osteocalcin is a valid biomarker for bone turnover and resorption. Aim: To analyze relationship between serum osteocalcin levels and periodontal status in osteoporotic risk women. Methods: A cross-sectional study was conducted on 70 postmenopausal women. Periodontal examination and serum osteocalcin levels was measured using ELISA method. Result: There is no difference of serum osteocalcin levels on osteoporotic, osteopenia, and normal subjects. Relationship between serum osteocalcin and clinical attachment loss was found on osteoporotic subjects. Conclusion: Relationship between serum osteocalcin levels and periodontal status was found on osteoporotic subjects.
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Jakarta: Fakultas Kedokteran Gigi Universitas Indonesia, 2017
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UI - Tesis Membership  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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Putri Rachmaniah Nur Hanisa
"Latar Belakang: Defek tulang yang besar membutuhkan pendekatan regenerasi tulang. Material hidroksiapatit (HA) dan gelatin telah banyak diteliti dan dikombinasikan karena sifatnya yang saling melengkapi dan meningkatkan aktivitas regenerasi tulang. Penambahan zat alami seperti propolis yang salah satunya memiliki kandungan Caffeic Acid Phenethyl Esters (CAPE) dapat menstimulasi pertumbuhan jaringan dan meningkatkan kadar biomarker pertumbuhan tulang. Oleh karena itu kombinasi biomaterial HA-gelatin-propolis yang belum pernah dilakukan sebelumnya, diharapkan dapat meningkatkan aktivitas regenerasi tulang yang dapat dilihat dari kadar alkali fosfatase (ALP) dan osteokalsin (OC) yang disekresikan oleh osteoblas.
Tujuan: Menganalisis kadar ALP dan OC pada medium kultur biakan sel osteoblas setelah dipajan elusi hidroksiapatit, gelatin, dan propolis 6% .
Metode: Human Osteoblast Cell line MG-63 dibiakan dan dibagi menjadi 6 kelompok pajanan yaitu kontrol, HA, propolis 6%, HA-gelatin, HA-propolis 6%, dan HA-gelatin-propolis 6%. Kadar ALP dan OC dianalisis pada medium kultur 7, 14, dan 21 hari setelah pemajanan kemudian dikuantifikasi menggunakan Uji ELISA.
Hasil: Kadar ALP dan OC seluruh kelompok mengalami peningkatan pada hari ke-7 dan 14 serta pengalami penurunan pada hari ke-21. Tidak terdapat perbedaan bermakna pada kelompok pajanan HA-gelatin-propolis 6% dibandingkan dengan kelompok kontrol. Kelompok HA, propolis 6%, dan HA-gelatin menunjukkan kadar yang lebih tinggi dari kontrol. Perbedaan yang bermakna secara statistik (p<0,05) terdapat pada kelompok propolis 6%. Kenaikan kadar ALP berkorelasi positif sedang dengan kenaikan kadar OC (r = 0,385, p=0,001).
Kesimpulan: Tidak terdapat perbedaan bermakna aktivitas proliferasi dan diferensiasi sel osteoblas yang dilihat dari kadar biomarker ALP dan OC pada pajanan elusi HA-gelatin-propolis 6% dibanding kelompok kontrol.

Background: Large bone defects require a bone regeneration approach. Hydroxyapatite (HA) and gelatin have been widely studied and combined because of their complementary properties and increasing bone regeneration activity. The addition of natural substances such as propolis, one of which contains Caffeic Acid Phenethyl Esters (CAPE) can stimulate tissue growth and increase levels of bone growth biomarkers. Therefore, the combination of HA-gelatin-propolis biomaterial that has never been done before, is expected to increase bone regeneration activity which can be seen from the levels of bone growth biomarkers alkaline phosphatase (ALP) and osteocalcin (OC) secreted by osteoblasts.
Objective: To analyze the levels of bone formation biomarkers such as ALP and OC in osteoblast cell culture medium after exposure to hydroxyapatite, gelatin, and propolis 6% elution.
Methods: This research is an in vitro laboratory study. Human Osteoblast Cell line MG-63 was cultured and divided into 6 groups, namely control, HA, propolis 6%, HA-gelatin, HA-propolis 6%, and HA-gelatin-propolis 6 %. ALP and OC levels were analyzed on culture medium 7, 14, and 21 days after exposure and then quantified using the ELISA test.
Results: ALP and OC levels in all groups increased on the 7th and 14th days and decreased on the 21st day. There was no significant difference in the HA-gelatin-propolis 6% exposure group compared to the control group. The 6% propolis and HA-gelatin groups showed higher levels than the control and a statistically significant difference (p<0.05) was found in the 6% propolis group. An increase in ALP levels was positively correlated with an increase in OC levels (r = 0.385, p = 0.001).
Conclusion: There was no significant difference in the proliferative and differentiation activity of osteoblasts as seen from the levels of biomarkers of ALP and OC in the HA-gelatin-propolis 6% elution exposure compared to the control group.
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Depok: Fakultas Kedokteran Gigi Universitas Indonesia, 2021
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UI - Skripsi Membership  Universitas Indonesia Library