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    <title>DSpace Collection:</title>
    <link>http://localhost:8080/xmlui/handle/123456789/8842</link>
    <description />
    <pubDate>Fri, 17 Apr 2026 03:23:48 GMT</pubDate>
    <dc:date>2026-04-17T03:23:48Z</dc:date>
    <item>
      <title>Polymorphisms of SLCO1B1 Gene in Sundanese Ethnic Population of Tuberculosis Patients in Indonesia</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9061</link>
      <description>Title: Polymorphisms of SLCO1B1 Gene in Sundanese Ethnic Population of Tuberculosis Patients in Indonesia
Authors: Santoso, Prayudi; Juliastuti, Henny; Melinda Nataprawira, Heda
Abstract: Background: The blood level of rifampicin, one of the tuberculosis (TB) drugs, depends on the organic anion&#xD;
transporting polypeptide 1B1 (OATP1B1) in hepatocytes. This protein is encoded by the solute carrier organic&#xD;
anion 1B1 (SLCO1B1) gene. Its genetic variation has been reported to have an impact on clinical outcomes and&#xD;
drug efficacy. However, the polymorphism in the SLCO1B1 gene has not been examined in Indonesia yet. We&#xD;
aimed to identify the frequency of polymorphism in SLCO1B1 gene among pulmonary TB patients in Bandung,&#xD;
Indonesia. Methods: Cross-sectional study was conducted in West Java. 145 pulmonary TB patients who were&#xD;
treated with first-line drugs treatment (including rifampicin 450 mg daily) were analyzed for polymorphism&#xD;
in SLCO1B1 gene. Patients aged between 18–64 years old and mainly came from Sundanese ethnic group&#xD;
(92.4%). Genetic variants were detected using Polymerase Chain Reaction (PCR) and Sanger sequencing.&#xD;
Results: Polymorphism of c.463C&gt;A(rs11045819) was not identified, while heterozygous and homozygous&#xD;
polymorphism of c.85-7793C&gt;T(rs4149032) were identified in 74 (51.0%) and 56 (38.6%) patients, respectively.&#xD;
The minor allele frequency (MAF) of T (mutant) allele of c.85-7793C&gt;T(rs4149032) was 64.13% (186/209),&#xD;
higher than in the general population, which the MAF of rs4149032 is 53.6% based on 1000 genome database.&#xD;
Conclusion: This study highlights the presence of different allele frequencies of polymorphisms within the population,&#xD;
which might affect treatment outcomes.&#xD;
Keywords: c.85-7793C&gt;T (rs4149032), c.463C&gt;A (rs11045819), drug transporter, gene polymorphism,&#xD;
West Java, Indonesia</description>
      <pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9061</guid>
      <dc:date>2022-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Lower Number and Percentage of Activated Natural Killer Cells in Colorectal Cancer Patients</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9060</link>
      <description>Title: Lower Number and Percentage of Activated Natural Killer Cells in Colorectal Cancer Patients
Authors: Vidyani, Amie; Abbas Nusi, Iswan; KholilI, Ulfa
Abstract: Background: Colorectal cancer is a type of cancer that begins in the colon and/or rectum tissue. Natural killer&#xD;
(NK) cells play a critical role in the first line of defense against infection and tumors, as well as in autoimmunity&#xD;
and hypersensitivity reactions. NK cells also play a role in regulating tumor cell growth and metastasis. The&#xD;
number and percentage of activated natural killer cells have been determined in patients with colorectal&#xD;
cancer and benign lesion. Methods: This was a cross-sectional observational analytic study. The number and&#xD;
percentage of activated NK cells in peripheral blood were determined using the flow cytometry method in&#xD;
50 samples from patients who underwent colonoscopy and obtained a mass as evidenced by histopathological&#xD;
examination. Results: Among the 50 samples, 24 samples included in the colorectal cancer group and 26 samples&#xD;
from benign lesion group. The mean number of NK cells in colorectal cancer was 161.71 ± 62.666 cells/μL,&#xD;
benign lesion was 553.92 ± 269.173 cells/μL. The mean percentage of activated NK cells in colorectal cancer&#xD;
was 2.82 ± 1.19%, benign lesion was 5.10 ± 2.48%. There was a significant difference in the number of NK cells&#xD;
and the percentage of activated NK cells between colorectal cancer and benign lesion patients (p = 0.000).&#xD;
Conclusion: The number and activity of NK cells decreases in patients with colorectal cancer.&#xD;
Keywords: The number of NK cells, percentage of activated NK cells, colorectal cancer, cancer.</description>
      <pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9060</guid>
      <dc:date>2022-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Diagnosis of Chronic Lymphocytic Leukemia Using iwCLL 2018 Compared with NCI-WG96 Criteria in Cipto Mangunkusumo Hospital: A Practical Consideration in Resource Limited Setting</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9056</link>
      <description>Title: Diagnosis of Chronic Lymphocytic Leukemia Using iwCLL 2018 Compared with NCI-WG96 Criteria in Cipto Mangunkusumo Hospital: A Practical Consideration in Resource Limited Setting
Authors: Sukrisman, Lugyanti; Rinaldi, Ikhwan
Abstract: Background: The diagnosis of chronic lymphocytic leukemia (CLL) is mainly based on blood count,&#xD;
morphology, and immunophenotyping. In Indonesia, the diagnosis is more challenging as the availability of&#xD;
immunophenotyping tests is limited. The European Society of Medical Oncology (ESMO) stated flowcytometry&#xD;
as a prerequisite to establishing diagnosis of CLL, meanwhile in the original International Workshop on Chronic&#xD;
Lymphocytic Leukemia (iwCLL) 2018 criteria, which has been widely accepted by physicians caring for patients&#xD;
with CLL, the diagnosis of CLL can be made in patients with cytopenia using bone marrow biopsy where&#xD;
flowcytometry test is not available. The aim of the study was to compare the utility of iwCLL 2018 compared&#xD;
with National Cancer Institute Working Group 96 (NCI-WG96) criteria in the diagnosis of CLL in Indonesia,&#xD;
especially in limited resource settings. Methods: The data of newly diagnosed CLL patients, including baseline&#xD;
demographic, clinical, and laboratory characteristics was retrieved retrospectively from medical records in Cipto&#xD;
Mangunkusumo General Hospital from 2015 until 2021. Diagnosis of CLL using iwCLL 2018 diagnostic criteria&#xD;
were then compared with NCI-WG96 criteria. Results: Thirty-eight patients were enrolled to this study. The&#xD;
median age was 59.5 years and dominated by males. Most of them were classified in the late-stage disease (63.4%&#xD;
in Binet C and about 70% in Rai III-IV). Four cases were CD5-negative CLL. Based on NCI-WG96 guideline,&#xD;
only 24 patients (63.2%) fulfilled all four criteria for CLL. Similarly, using the iwCLL 2018 flowcytometric&#xD;
criteria without biopsy data, 26 patients (68%) were diagnosed as CLL. However, if bone marrow biopsy in&#xD;
patient with cytopenia was taken into account, all patients (100%) can be confirmed as CLL. Conclusion: The&#xD;
iwCLL 2018 criteria which included bone marrow biopsy in the presence of cytopenia was more applicable to&#xD;
establish the diagnosis of CLL in Indonesia where flowcytometry is not available.&#xD;
Keywords: chronic lymphocytic leukemia, diagnosis, NCI-WG96 criteria, IWCLL 2018 criteria</description>
      <pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9056</guid>
      <dc:date>2022-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Antiviral Treatment in COVID-19 Outpatients: A Systematic Review of Randomized Controlled Trials</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9053</link>
      <description>Title: Antiviral Treatment in COVID-19 Outpatients: A Systematic Review of Randomized Controlled Trials
Authors: Setyo Budi, David; Oktavian, Puguh; Pudy Asmarawati, Tri
Abstract: Background: Most COVID-19 patients have mild or moderate illnesses that can progress to severe illness,&#xD;
leading to hospitalization and/or mortality. The use of antivirals to prevent the progression of COVID-19 in nonhospitalized&#xD;
patients shows conflicting result and efficacy remain unclear. This study evaluates the efficacy and&#xD;
safety of antivirals therapy in COVID-19 outpatients. Methods: Search were conducted in Pubmed, ScienceDirect,&#xD;
Cochrane Library, Springer, medRxiv, Journal Storage [JSTOR], and Directory of Open Access Journals [DOAJ]&#xD;
for articles investigating antivirals in COVID-19 outpatients. In addition, clinical and virological outcomes,&#xD;
COVID-19 hospitalization, all caused mortality, and adverse events were assessed. Results: Thirteen studies&#xD;
were included in this review. The consecutive data from these studies suggested that favipiravir is more optimally&#xD;
used in early disease, but improvement in symptoms shows inconsistent results. Meanwhile, molnupiravir shows&#xD;
consistent results, which can reduce hospitalization and mortality risk. In addition, remdesivir and nirmatrelvirritonavir&#xD;
have the potential to prevent the progression of COVID-19 in outpatients, but the data provided in&#xD;
this study are very limited. Finally, there is no significant difference in serious and non-serious adverse events,&#xD;
highlighting that antivirals have a good safety profile. Conclusion: This study provides an overview of the role&#xD;
of various antivirals therapy in COVID-19 outpatients. Molnupiravir, remdesivir, and nirmatrelvir-ritonavir&#xD;
have shown potential to prevent the progression of COVID-19 in early disease. However, this review was based&#xD;
on very limited data. Therefore, further clinical trials are needed to confirm this finding.&#xD;
Keywords: COVID-19, SARS-COV-2, antiviral, outpatients, systematic review</description>
      <pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9053</guid>
      <dc:date>2022-01-01T00:00:00Z</dc:date>
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