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All Journal Tropical Medicine Journal International Journal of Biosciences and Biotechnology Journal of the Medical Sciences (Berkala Ilmu Kedokteran) Jurnal Gizi Klinik Indonesia Biota: Jurnal Ilmiah Ilmu-Ilmu Hayati Jurnal Kesehatan Masyarakat Indonesian Journal of Urology Jurnal Farmasi Klinik Indonesia Indonesian Journal of Biotechnology Jurnal Kedokteran BERITA BIOLOGI Majalah Obstetri dan Ginekologi Jurnal Teknologi Laboratorium Universa Medicina Paediatrica Indonesiana JURNAL MANAJEMEN DAN PELAYANAN FARMASI (Journal of Management and Pharmacy Practice) Jurnal Gizi Klinik Indonesia Jurnal Kesehatan Prima Acta Biochimica Indonesiana Indonesian Journal of Clinical Pathology and Medical Laboratory (IJCPML) Pena Medika : Jurnal Kesehatan
Ahmad Hamim Sadewa
Universitas Gadjah Mada
Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemistry Environmental Science Health Professions Immunology & microbiology Materials Science & Nanotechnology Medicine & Pharmacology Neuroscience Nursing Public Health Veterinary Other

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Assessment of the application level of radiation protection and awareness of radiation safety regulations among the radiographers at Yogyakarta Special Region, Indonesia Ahmad Hamim Sadewa, Ahmad Rafiq Mohammad Abu Arrah Arif Faisal
Journal of the Medical Sciences (Berkala Ilmu Kedokteran) Vol 43, No 02 (2011)
Publisher : Journal of the Medical Sciences (Berkala Ilmu Kedokteran)

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Abstract

A strong relation between cancers and radiation exposure has been reported. Radiation may damage DNA in thecell. Therefore, radiation protection program must be applied in the radiology department. Morover, the radiographershould have high level of awareness and risk assessment for radiation. Personal radiation monitoring is one of themain radiation protection, especially for pregnant worker and her fetus. This study was conducted to evaluate theapplication, awareness and risk assessment levels of radiation protection among radiographers at hospitals inYogyakarta Special Region, Indonesia. This was a descriptive study, applying a cross sectional survey at hospitals inYogyakarta. The subjects were radiographers of both governmental and private hospitals. There were 101 respondentsfrom a total of 124 radiographers. The data obtained were tabulated and analyzed using Chi Square test. The studyrevealed that 69.3% of the respondents had low application level of radiation protection, 19.8% did not know themeaning of ALARA (As Low As Reasonably Achievable), 50.5% were not aware of Inverse Square Law. The studyalso reported that 36.6% of the respondents did not know the amount of radiation that entered their body last year,61.4% of radiographers thought that the risk assessment of radiation was not enough, 18.8% of radiographerswere never use any radiation monitoring device, and 90.1% stated that there was no additional protection orradiation monitoring to the pregnant radiographer. However, there were no significant differences between durationof working, type of imaging modality, academic level, and training course for radiation protection. In conclusion,there was no difference in the application, awareness, and risk assessment levels of radiation protection among theradiographers at hospital in Yogyakarta Special Region between duration of working, type of medical imaging modality,academic level, and training on radiation protection. In addition, the application, awareness, and risk assessmentlevels of radiation protection were not sufficient.Key words: radiation protection – ALARA – radiographer – hospital – risk assessment
Aldose reductase genetic polymorphism is a risk factor of diabetics retinopathy among type 2 diabetes mellitus in Yogyakarta, Indonesia Tasmini, Jujuk Anton Cahyono Ahmad Hamim Sadewa
Journal of the Medical Sciences (Berkala Ilmu Kedokteran) Vol 43, No 02 (2011)
Publisher : Journal of the Medical Sciences (Berkala Ilmu Kedokteran)

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Abstract

Diabetes mellitus (DM) is a metabolic syndrome characterized by hyperglycemia and glucose intolerance, due toinsulin resistance, insulin deficiency, or both. Diabetics retinopathy (DR) is a DM complication due to retinal abnormality,that causes vision reduction and even blindness. The association between DR and aldose reductase C-106T (ALR C-106T) gene polymorphism has been reported in previous studies. This genetic polymorphism increases the sorbitollevel inside erythrocyte and pericyte in the retinal membrane that leads to weakness of retinal capillary vessel andmicroaneurism. The aim of this study was to know the presence of ALR C-106T gene polymorphism and its frequencydistribution among diabetics Javanese patients in Dr. Sardjito General Hospital Yogyakarta, Indonesia. In addition,this study also aimed to analyze the difference of erythrocytes osmotic fragility (EOF) among ALR genotypes in type2 diabetics patients with DR and without DR and to analyze whether ALR genetic polymorphism is a risk factor ofDR in type 2 diabetic patients. This was a case control study that involved 40 diabetics patients with DR as case and40 diabetics patients without DR as control groups. The C-106T ALR gene polymorphism was determined bypolymerase chain reaction-restriction fragment length polymorphism (PCR–RFLP) method. Erythrocytes osmoticfragility was analyzed using spectrophotometer. Genotype and allele distributions were analyzed using x2 and otherdata were analyzed using independent t-test and Mann-Whitney, with p<0.05 was considered as significantlydifferent. The results showed that in type 2 diabetics patients with DR, 33 patients (82.5%) were CC homozygoteindividuals and 7 patients (17.5%) were CT heterozygote individuals. In type 2 diabetics patients without DR, 27patients (67.5%) were CC homozygote individuals and 13 patients (32.5 %) were CT heterozygote individuals. Thegenotype and allele distributions were not significantly different between two groups (p=0.121 for genotype,p=0.151 for allele). Odds Ratio of genotype was 2.270 while allele was 2.023. Erythrocytes osmotic fragility of CCgenotype was higher than CT genotype (p=0.047). In conclusion, there was no significant difference between CCand CT genotype distribution among type 2 diabetics patients with and without DR. Erythrocyte osmotic fragility ofCC genotype was higher than CT genotype. C-106T gene polymorphism was a risk factor of DR in type 2 diabeticpatients.Key words : ALR genes – polymorphism - type 2 DM - diabetic retinopathy - erythrocytes osmotic fragility
Relation between -carotene and ferritin upon malondialdehyde in Javanese male smoker Sunarti, Naomi Yoshuantari Ahmad Hamim Sadewa
Journal of the Medical Sciences (Berkala Ilmu Kedokteran) Vol 43, No 01 (2011)
Publisher : Journal of the Medical Sciences (Berkala Ilmu Kedokteran)

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Abstract

Smoking of cigarette can cause additional free radicals. Oxidative damage is resulted from the accumulation of freeradicals in the body. Malondialdehyde (MDA) is the end product of free radicals, a marker of oxidative damage. -carotene is pro-vitamin A, an antioxidant known to quench singlet oxygen. Ferritin is thought to release excessiveiron in smokers, thereby increasing the oxidative stress. The aim of the study is to evaluate the relation between -carotene and ferritin toward MDA level in Javanese smokers. This study was carried out in a case-control, crosssectional design nested with cluster sampling. Participants were Javanese smokers and non-smokers in Purworejodistrict, Central Java. Samples and data were obtained secondarily. The results were analyzed using independentsamples t-test and linear regression. The results showed that there was very weak negative correlation between -carotene with MDA (R square=0.013; p value=0.320) and very weak positive correlation between ferritin withMDA (R square=0.043; p value=0.067). There was no statistically significant relation of -carotene with MDA.Ferritin level was marginally influential upon MDA level as the marker of lipid peroxidation between smokers andnon-smokers. Aging apparently became the confounding variable by influencing the lipid peroxidation more efficientlythan smoking itself (p = 0.013). In conclusion, there was no significant relation between -carotene and ferritinwith MDA in smokers.Key words : smoking – cigarette – β-carotene – ferritin – malondialdehyde
Polymorphism of vascular endhothelial growth factor (VEGF) gene insertion/ deletion -2549 as risk factor of diabetic retinophathy in Javanese patients with type 2 diabetes Maliyah Madiyan, Jems Kifen Roget Maay Ahmad Hamim Sadewa
Journal of the Medical Sciences (Berkala Ilmu Kedokteran) Vol 44, No 02 (2012)
Publisher : Universitas Gadjah Mada

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Abstract

Diabetic retinopathy (DR) is a visual disorder caused by the diabetic microvascular complications.Genetic polymorphism in the vascular endothelial growth factor (VEGF) gene plays an importanrole in the susceptibility of DR. The aim of this study was to evaluate the association of thepolymorphism of VEGF gene insetion/deletion (I/D) -2549 with DR in Javanese type 2 diabetesmellitus (DM) patients. This was a case control study involving 40 Javanese type 2 DM patientswith DR as case subjects and 40 Javanese type 2 DM patients without DR as control subjects.Type 2 DM patients with DR were recruited from Eye Polyclinic, whereas type 2 DM patientswithout DR were recruited from Endocrine Polyclinic of Dr. Sardjito General Hospital, Yogyakarta.Genotyping of VEGF gene I/D-2549 was conducted using PCR-RFLP method. Plasma VEGFlevels were measured using Enzym-Linked Immunosorbent Assay (ELISA). The genotype distributionof DD (67.5%) and the allele frequency of D (82.5%) in type 2 DM patients with DR was higherthan those without DR (27.5% for DD genotype and 56.3% for D allele). The OR of DD and IDgenotypes versus II genotype between type 2 DM patients with DR and without DR was 6.882(95%CI: 0.789-60.060; p=0.048), whereas OR for the D allele versus I allele between type 2 DMpatients with DR and without DR was 3.667 (95%CI: 1.773-3.667; p=0.000). The plasma VEGFlevels of DD genotype (92.16±49.73 pg/mL) were significantly higher than ID genotype(42.70±33.29 pg/mL) in type 2 DM patients (p=0.000). In conclusion, the polymorphism ofVEGF gene I/D -2549 is associated with DR in Javanese type 2 DM patients. The DD genotypeand D allele of the VEGF gene polymorphism are the risk factor of DR in those patients. Theassociation of the polymorphism of VEGF gene with DR may be explained with the high plasmaVEGF level.Keywords: vascular endothelial growth factor (VEGF) - polymorphism - diabetes - retinopathy- Javanese patients
A Novel Variant of HOXA10 gene, Ser19Cys, among Patients with Endometriosis and its Relationship with the Severity of the Disease Hutajulu, Pinda; Dasuki, Djaswadi; Sadewa, Ahmad Hamim; Utoro, Totok
Indonesian Journal of Biotechnology Vol 18, No 1 (2013)
Publisher : Universitas Gadjah Mada

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Abstract

Endometriosis is a gynecological disease associated with inherited genetic traits. HOXA10 gene whichis expressed in uterine plays an important role in the pathogenesis of endometriosis. The protein affects thedevelopment of pinopodes as a biomarker of endometrial receptivity in endometriosis.The aim of this study isto examine if there is a mutation or polymorphism within HOXA10 gene among patients with endometriosis.Thirty twopatients and 32 healthy women were recruited as subjects of this study. The exon 2 of HOXA10which covers most of coding region was amplifi ed using PCR. The presence of a mutation or polymorphismwas detected by direct seguencing. The distribution of genotype and allele was analyzed using Chi square test with p<0.05 is considered as signifi cantly different. A novel heterozygous variant within exon 2 of HOXA10 which substitute an adenine into thymine was detected at base position 55. This missense alteration changed amino acid serine to cystein (Ser19Cys). Interestingly, this variant was detected in 12 endometriosis cases (38%) but none in control. Patients carry HOXA10 Ser19Cys variant were associated with dismenorea and more frequent in stage I endometriosis. The role of this variant in the function of HOXA10 protein and frequency among Indonesians need to be clarifi ed. We found a novel heterozygous HOXA10 gene variant, Ser19Cys.The genotype frequency is 38% among endometriosis patients but none in control. This variant found in patient with dismenore and endometriosis stage 1.Key words: HOXA10 gene, endometriosis, Ser19Cys polymophism
Genetic Variation of Apolipoprotein E (ApoE) in Surabaya, Palu and Alor Populations of Indonesia Hastuti, Pramudji; Sofro, Abdul Salam Mudzakir; Asdie, Ahmad Husain; Sadewa, Ahmad Hamim
Indonesian Journal of Biotechnology Vol 16, No 2 (2011)
Publisher : Universitas Gadjah Mada

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Abstract

AbstractApolipoprotein E (ApoE) has been considered to play an important role in cardiovascular disorders.Several studies reported that genetic variation in ApoE locus influence plasma lipoprotein level. The objectivesof this study was to compare the frequency of ApoE genotypes and alleles in some populations of Indonesia.One hundred and ninety five voluntarily unrelated apparently healthy individuals were recruited fromSurabaya, Palu and Alor representing the western, middle and eastern populations of Indonesia, respectively.Blood samples were collected from each subject for DNA extraction. The common allelic variants of ApoE werescreened using polymerase chain reaction (PCR) and restriction fragment length polymorphism. Three allelesi.e. ε2, ε3 and ε4 were identified and five genotypes i.e. ApoE ε2/ε2, ApoE ε2/ε3, ApoE ε3/ε3, ApoE ε2/ε4, ApoE ε3/ε4 were found in three populations studied, while ApoE ε4/ε4 was absent in Surabaya, representing the westernpopulations of Indonesia. The frequency of ε2, ε3 and ε4 alleles in the western population were 0.208, 0.701and 0.092 respectively; in the middle population were 0.242, 0.618 and 0.140 respectively and in the easternpopulation of Indonesia were 0.267, 0.466 and 0.267 respectively. The highest frequency of ε2 and ε4 allelewas found in the eastern population of Indonesia. The distribution of ε2 allele were not significantly differentamong all Indonesian populations, but significantly different were found in ε3 and ε4 allele in the easternpopulation compared to those in the western and middle populations of Indonesian. It can be concluded thatthe frequency of three ApoE alleles in the western and middle populations of Indonesia was not significantlydifferent however, significantly different was observed in the frequency of ApoE ε3 and ε4 alleles from theeastern compared to those in the western and middle populations of Indonesia.Keywords : Apolipoprotein E; genotypes; allele frequency; populations of Indonesia
Apolipoprotein E as Risk Factor for Coronary Heart Disease Hastuti, Pramudji; M Sofro, Abdul Salam; Asdie, Ahmad Husain; Sadewa, Ahmad Hamim
Indonesian Journal of Biotechnology Vol 18, No 1 (2013)
Publisher : Universitas Gadjah Mada

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Abstract

Allelic variation of apolipoprotein E (apo E) has been shown to infl uence the concentrations of total cholesterol and low density lipoprotein cholesterol (LDL-C) and considered to play a role as one of risk factors for coronary heart disease (CHD). The aim of this study was to examine the relationship between Apo E polymorphism and the risk of CHD. Blood samples were collected from 33 CHD patients in Dr. Sardjito Hospital Yogyakarta, and 38 apparently healthy control individuals in a cross sectional study. The common allelic variants of ApoE were screened employing polymerase chain reaction and restriction fragment length polymorphism. The results obtained were analyzed by t-test and signifi cantly different if p <0.05 and risk factor was calculated by odd ratio. Frequency of ApoE ε2, ε2 and ε4 alleles in CHD patients were 12.1%, 69.7% and 18.2% while in controls were 18.4%, 72.4% and 9.2% respectively. Dyslipidemia condition was a strongrisk factor for CHD. By controlling lipid profi le and applying multifactorial statistic analysis, it was shown that ε4 gene carrier was the risk factor for CHD, but not in triglyceride level, whereas ε2 carrier gene was not the risk factor for CHD. Dislipidemia was the risk factor for CHD and ApoE ε4 gene carrier was the risk factor for CHD.Key words: apolipoprotein E, ApoE ε4 gene carrier, coronary heart disease, dyslipidemia.
RET single nucleotide polymorphism in Indonesians with sporadic Hirschsprung’s disease Saryono, Saryono; Rochadi, Rochadi; Lestariana, Wiryatun; Artama, Wayan T; Sadewa, Ahmad Hamim
Universa Medicina Vol 29, No 2 (2010)
Publisher : Faculty of Medicine, Trisakti University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18051/UnivMed.2010.v29.71-77

Abstract

The tyrosine kinase receptor RET, which is the protein product of the RET gene, is involved in the development of the mammalian nervous system that causes Hirschsprung’s disease (HSCR). RETs are cell surface molecules that are expressed in cells derived from the neural crest. The purpose of this study was to investigate the polymorphism of the RET gene in HSCR in the Yogyakarta population. Genomic DNA was extracted from surgically removed bowel tissues of 54 unrelated HSCR patients. Exon 2 of the RET gene was amplified by polymerase chain reaction (PCR) and analyzed by restriction fragment length polymorphism (RFLP). Molecular results were compared with clinical performance of Hirschsprung patients. RET polymorphism was detected in exon 2 in all of the 54 Indonesian HSCR patients. The allelic distribution of the c135GàA polymorphism in the RET exon 2 indicated that the A allele was more frequent in patients than in control individuals (chi-square test, p= 0.001). Thus the RET variant allele A is over-represented in patients affected with the HSCR phenotype. Polymorphism of exon 2 of the RET gene was found in sporadic Hirschsprung’s disease in the Yogyakarta population, which suggests that the RET gene plays important roles in the pathogenesis of HSCR.
Kontrol Glikemik dan Prevalensi Gagal Ginjal Kronik pada Pasien Diabetes Melitus Tipe 2 di Puskesmas Wilayah Provinsi DIY Tahun 2015 Ningrum, Vitarani Dwi Ananda; Ikawati, Zullies; Sadewa, Ahmad Hamim; Ikhsan, Mohammad Robikhul
Indonesian Journal of Clinical Pharmacy Vol 6, No 2 (2017)
Publisher : Indonesian Journal of Clinical Pharmacy

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (621.312 KB) | DOI: 10.15416/ijcp.2017.6.2.78

Abstract

Pengendalian glikemik yang baik pada diabetes melitus tipe 2 (DMT2) terbukti dapat mencegah penyakit komplikasi akibat DMT2. Puskesmas sebagai sarana pelayanan kesehatan primer merupakan garda terdepan yang diharapkan dapat memberikan pelayanan pengelolaan DMT2 dengan baik untuk mencegah penyakit komplikasi seperti penyakit gagal ginjal kronik (GGK). Kejadian GGK yang seringkali tanpa gejala spesifik serta keterbatasan pemeriksaan diagnostik di puskesmas menyebabkan keterlambatan diagnosa GGK maupun pengelolaan terapi yang sub-optimal. Penelitian ini bertujuan menganalisis kontrol glikemik dan kejadian GGK pada pasien DMT2 di puskesmas serta faktor pasien yang memengaruhi kontrol glikemik dan kejadian GGK. Penelitian potong-lintang pada 6 puskesmas di Yogyakarta tahun 2015 ini melibatkan pasien DMT2 dewasa tanpa riwayat gagal hati kronik. Parameter kontrol glikemik menggunakan Glukosa-Darah-Puasa (GDP), Glycated-Albumin (GA), atau hemoglobin terglikasi (HbA1C), sedangkan nilai eLFG digunakan sebagai dasar klasifikasi GGK. Sebanyak 101 pasien dengan rata-rata usia 50,75±6,73 tahun terlibat dalam penelitian. Kontrol glikemik kategori baik ditemukan hanya pada 13,86% pasien, sedangkan 12,87% pasien mengalami GGK. Tidak ada faktor pasien yang memengaruhi kontrol glikemik. Sementara itu, usia dan durasi DMT2 berkorelasi dengan kejadian GGK (p<0,01). Berdasarkan penelitian ini, kontrol glikemik yang buruk dapat meningkatkan kemungkinan kejadian GGK sebesar 63,64%. Oleh karena itu, diperlukan strategi pengelolaan DMT2 maupun pencegahan GGK yang lebih baik termasuk penyediaan fasilitas pemeriksaan yang memadai untuk meminimalkan kejadian clinical inertia di puskesmas.
Polimorfisme gen ferroportin (FPN1) -1355 G/C sebagai faktor risiko anemia defisiensi besi pada ibu hamil Istiqomah, Nor; Umarghanies, Sarah Safira; Farmawati, Arta; Sadewa, Ahmad Hamim; Soesilo, Yuliana Heri; Damayanti, Kusumadewi Eka; Indarto, Dono
Jurnal Gizi Klinik Indonesia Vol 9, No 4 (2013): April
Publisher : Minat S2 Gizi dan Kesehatan, Prodi S2 IKM, FK-KMK UGM

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (201.17 KB) | DOI: 10.22146/ijcn.18364

Abstract

Background: According to WHO data, prevalence of anemia pregnancy in Indonesia is 44.3%, it’s higher than world prevalence (41.8%). Ferroportin (FPN1) is one of important iron exsporter for iron absorption, release, and recycle inside the body. The varian of FPN1-1355 G/C in promoter region, leads to increased of ferroportin expression and iron export, increased cellular iron needs, overexpression of soluble transferrin receptor (sTfR), decrease hemoglobin (Hb) and erythrocyte indices that manifest to iron deficiency anemia (IDA).Objective: This research will study the frequency of FPN1-1355 G/C polymorphism as a risk factor of IDA in pregnant women in Indonesia.Method: The research design was a case and control study. Blood samples were taken from 26 pregnant women with anemia and 48 pregnant women without anemia. FPN1-1355G/C polymorphism were determined using PCR-RFLP method. sTfR and ferritin level were measured with ELISA. Hemoglobin, erythrocyte indices, and sTfR level were compared among genotype group, then statistically analyzed using independent sample t-test and one way ANOVA. Bivariat analysis of Pearson test was conducted to analyze correlation between level of blood Hb and ferritin in pregnant women (p<0.05).Results: FPN1-1355 G/C polymorphism with frequency in pregnant women with IDA and in pregnant women with anemia non IDA were 100% and 95.2%, respectively (p=0.710; OR=1.600; 95%CI: 0.296-8.653). The mean of Hb level and erythrocyte indices in subjects carrying C allele were lower than subjects carrying only G allele although Hb level is not significantly different (p>0.05). The sTfR and hepcidin level in subjects carrying C allele were higher than subjects carrying only G allele (p<0.05). Conclusion: In this study the FPN1 gene promoter -1355 G/C polymorphism was not a risk factor for anemia, but it was a risk factor for iron deficiency anemia in pregnant women.
Co-Authors . Harapan . HERNAYANTI . Mustofa . Mustofa . Syahrul Abdul Salam M Sofro, Abdul Salam Abdul Salam M. Sofro Abdul Salam Mudzakir Sofro Abdul Salam Mudzakir Sofro, Abdul Salam Mudzakir Abdurahman Laqif Abdurahman Laqif Abdus Samik Wahab Ahmad Husain Asdie Ahmad Husain Asdie Ahmad Husain Asdie Ajeng Viska Icanervilia Akhmad Kharis Nugroho Anggelia Puspasari Anggoro Budi Hartopo Arif Faisal Arif Faisal Arta Farmawati Awal Prasetyo Bai Apris Bambang Hariono Bambang Hariono Bansai Immanuel Bernadia Branitamahisi Bernadia Branitamahisi Budi Yuli Setianto Cahyono Hadi Cahyono Hadi Citra Maharani Darojatun Ida Demas Bayu Handika Dessy Rakhmawati Emril Dewajani Purnomosari Dian Caturini Sulistyonigrum Didik Setyo Heriyanto Djaswadi Dasuki Djaswadi Dasuki Djaswadi Dasuki Djaswadi Dasuki Dono Indarto Dono Indarto DONO INDARTO Dyah Wulan Anggrahini Emy Huriyati Endang Mutiawati Rahayuningsih* Fransisca Shinta Maharini Hananta, Linawati Hari Kusnanto Hasan Sjahrir Hemi Sinorita Hendi Wicaksono Hernayanti , Hernayanti HERNAYANTI HERNAYANTI I Gusti Ayu Nyoman Danuyanti I NYOMAN MANTIK ASTAWA Ida Ayu Preharsini Ida Ayu Preharsini Kusuma Ika Rahayu Ika Setyawati Ikhsan, M. Robikhul Ikhsan, Mohammad Robikhul Imran Imran Indwiani Astuti Indwiani Astuti Indwiani Astuti Inna Narayani Iskandar Zakaria Jenny Hidayat Jontari Hutagalung Kik Hao Samuel Kris Herawan Timotius Kusumadewi Eka Damayanti Kusumadewi Eka Damayanti Kusumadewi Eka Damayanti Lina Choridah Lucia Krisdinarti Lukman Hakim M. Robikhul Ikhsan Maliyah Madiyan Maria Dara Novi Handayani, Maria Dara Novi Marsetyawan HNE Soesatyo Mega Tyas Prihatin Mus, Rosdiana Mustofa Mustofa Nor Istiqomah Nor Istiqomah Nor Istiqomah Nor Sri Inayati Nor Sri Inayati Nova Dian Lestari Novijanti Rintis P. Purwono Pinda Hutajulu Pinda Hutajulu, Pinda Pramana, Abrory Agus Cahya Pramudji Hastuti Pramudji Hastuti Pramudji Hastuti Pramudji Hastuti Pramudji Hastuti Pramudji Hastuti, Pramudji Prasetyastuti Prasetyastuti Prasetyastuti, . Rahmaningsih Mara Sabirin Rasmaya Niruri Ratih Feraritra Danu Atmaja Rina Pratiwi Pudja I. A Rina Susilowati Rochadi Rochadi Rochadi Rochadi, Rochadi Rubi, Dianandha Septiana S. Supargiyono Sarah Safira Umarghanies Saryono Saryono Satyagraha Ari Winasti Seto Priyambodo Setyo Purwono Sofia Mubarika Haryana Sofia Mubarika Haryana Sri Sutarni Stefani Santi Widhiastuti Stefani Santi Widhiastuti Subagus Wahyuono Sukarti Moeljopawiro Sunarti Sunarti Sunarti, Sunarti Sunarto Ang Tasmini - Teguh Aryandono Titiek Suhardi Haripurnomo Kushadiwijaya Hidayati Totok Utoro Totok Utoro Triwibowo A. Garjito Umarghanies, Sarah Safira Utami, Rizki Fajar Vitarani Dwi Ananda Ningrum Vitria Sari Dewi Waode Astria Sahrani Wasilah Rochmah wayan T Artama wayan T Artama Wayan Tunas Artama Wiryatun Lestariana Wiryatun Lestariana, Wiryatun Yuliana Heri Soesilo Yuliana Heri Soesilo Yuliana Heri Soesilo Yuliani, Fara Silvia Yunilistiaingsih Yunilistiaingsih Yunilistiaingsih, Yunilistiaingsih Yuningtyaswari Yuningtyaswari Zullies Ikawati