Endang Mahati

Endang Mahati


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 September 2014 in Clinical and Experimental Nephrology
Verified
Journal Article
Closed access
PDF file
SUSulistiyati Bayu Utami
Sulistiyati Bayu Utami
EMEndang Mahati
Endang Mahati
PLPeili Li
Peili Li
NMNani Maharani
Nani Maharani
NINobuhito Ikeda
Nobuhito Ikeda
IHIchiro Hisatome
Ichiro Hisatome

1 September 2015 in Journal of Molecular and Cellular Cardiology
Verified
Journal Article
Closed access
PLPeili Li
Peili Li
YKYasutaka Kurata
Yasutaka Kurata
NMNani Maharani
Nani Maharani
EMEndang Mahati
Endang Mahati
KHKatsumi Higaki
Katsumi Higaki
IHIchiro Hisatome
Ichiro Hisatome

1 February 2018 in Journal of Molecular and Cellular Cardiology
Verified
Journal Article
Closed access
PLPeili Li
Peili Li
YKYasutaka Kurata
Yasutaka Kurata
EMEndang Mahati
Endang Mahati
HNHaruaki Ninomiya
Haruaki Ninomiya
KHKatsumi Higaki
Katsumi Higaki
IHIchiro Hisatome
Ichiro Hisatome

6 June 2025 in Journal of Food Science
Verified
Journal Article
Closed access
TMTsamaroh Azzah Mukarromah
Tsamaroh Azzah Mukarromah
NRNinik Rustanti
Ninik Rustanti
EMEndang Mahati
Endang Mahati
SUSuparmi
Suparmi
FAFITRIYONO AYUSTANINGWARNO
FITRIYONO AYUSTANINGWARNO

4 April 2024 in Vaccine
Verified
Journal Article
Open access
ANAsrawati Nurdin
Asrawati Nurdin
YNYetty Movieta Nency
Yetty Movieta Nency
MMMartira Maddeppungeng
Martira Maddeppungeng
RSRini Sekartini
Rini Sekartini
RSRini Mulia Sari
Rini Mulia Sari
SOSoedjatmiko
Soedjatmiko
Bio Farma has developed a recombinant protein subunit vaccine (IndoVac) that is indicated for active immunization in population of all ages. This article reported the results of the phase 3 immunogenicity and safety study in Indonesian adults aged 18 years and above. We conducted a randomized, active-controlled, multicenter, prospective intervention study to evaluate the immunogenicity and safety of IndoVac in adults aged 18 years and above. Participants who were SARS-CoV-2 vaccine-naïve received two doses of either IndoVac or control (Covovax) with 28 days interval between doses and were followed up until 12 months after complete vaccination. A total of 4050 participants were enrolled from June to August 2022 and received at least one dose of vaccine. The geometric mean ratio (GMR) of neutralizing antibody at 14 days after the second dose was 1.01 (95 % confidence interval (CI) 0.89-1.16), which met the WHO non-inferiority criteria for immunobridging (95 % CI lower bound > 0.67). The antibody levels were maintained through 12 months after the second dose. The incidence rate of adverse events (AEs) were 27.95 % in IndoVac group and 32.15 % in Covovax group with mostly mild intensity (27.70 %). The most reported solicited AEs were pain (14.69 %) followed by myalgia (7.48 %) and fatigue (6.77 %). Unsolicited AEs varied, with each of the incidence rate under 5 %. There were no serious AEs assessed as possibly, probably, or likely related to vaccine. IndoVac in adults showed favourable safety profile and elicited non-inferior immune response to Covovax. (ClinicalTrials.gov: NCT05433285, Indonesian Clinical Research Registry: INA-R5752S9).

28 February 2021 in Folia Medica
Verified
Journal Article
Open access
PDF file
NTNurina Tyagita
Nurina Tyagita
EMEndang Mahati
Endang Mahati
ASAzizah Hikma Safitri
Azizah Hikma Safitri
Introduction: Antidiabetic medicinal plants are increasingly used in the treatment of diabetes as they are generally assumed to pro-duce minimal side effects. Okra is a quercetin-containing plant which can induce pancreas regeneration and has antidiabetic effect. There has been a lot of research that demonstrate that purple okra contains more quercetin than green okra. Aim: To demonstrate the advantages of purple okra over green okra on the diabetic markers improvement in diabetic rats. Materials and methods: Fifteen male 2-month-old Wistar rats were injected intraperitoneally with 65 mg streptozotocin and 110 mg niacinamide. Their blood glucose levels were measured three days after the injection. The induction of diabetes was deemed  successful if the glucose level of the rats got higher than 250 mg/dL, and then such rats were considered diabetic. The diabetic rats were divided into three groups: an acarbose group, a purple okra powder group, and a green okra powder group. The latter two were given, respectively, purple and green okra powder for 28 days. Blood serum was taken to examine the fasting blood glucose, insulin, HOMA-B and GLUT-4 levels. Pancreas was examined histologically for damage using hematoxylin eosin staining.  Results: Fasting blood glucose, insulin, HOMA-B, and GLUT-4 levels of diabetic rats that received purple okra powder (p<0.05) were better than those of the rats that received green okra powder. The least damage (p<0.05) to pancreatic beta cells was found in the purple okra powder group. Conclusions: Purple okra is superior to green okra in terms of improving the diabetic markers of rats.