1.Unlocking the growth potential:harnessing the power of synbiotics to enhance cultivation of Pleurotus spp.
PATIL RESHMA ; Aizi Nor Mazila RAMLI ; XUAN Shu ANG ; XIN Zhi NG ; Nur Izyan Wan AZELEE ; BHUYAR PRAKASH
Journal of Zhejiang University. Science. B 2024;25(4):293-306
The oyster mushroom(Pleurotus spp.)is one of the most widely cultivated mushroom species globally.The present study investigated the effect of synbiotics on the growth and quality of Pleurotus ostreatus and Pleurotus pulmonarius.Different synbiotics formulations were applied by spraying mushroom samples daily and measuring their growth parameters,yield,biological efficiency,proximate composition,mineral content,total phenolic content(TPC),and diphenyl-1-picryl-hydrazyl(DPPH)radical scavenging activity.Results demonstrated that the most significant yield of oyster mushrooms was harvested from synbiotics sprayed with inulin and Lactobacillus casei(56.92 g).Likewise,the highest biological efficiency obtained with a similar synbiotic was 12.65%.Combining inulin and L.casei was the most effective method of improving the mushrooms'growth performance and nutrient content in both samples.Furthermore,synbiotics that combined inulin and L.casei resulted in the highest TPC(20.550 mg gallic acid equivalent(GAE)/g dry extract(DE))in white oyster mushrooms(P.ostreatus).In comparison,in grey mushroom(P.pulmonarius)the highest TPC was yielded by L.casei(1.098 mg GAE/g DE)followed by inulin and L.casei(1.079 mg GAE/g DE).The DPPH results indicated that the oyster mushroom could be an efficient antioxidant.The results revealed that applying synbiotics improved the mushrooms'quality by increasing their antioxidant capacity with higher amounts of phenolic compounds and offering better health benefits with the increased levels of mineral elements.Together,these studies demonstrated the potential of using synbiotics as a biofertilizer,which is helpful for mushroom cultivation;therefore,it might solve the challenge of inconsistent quality mushroom growers face.
2.Neonatal outcomes of pregnancies complicated by maternal Hyperthyroidism
Adlina Awanis Abdullah ; Noraida Ramli ; Najib Majdi Yaacob ; Suhaimi Hussain
Journal of the ASEAN Federation of Endocrine Societies 2022;37(2):15-22
Objective:
This study aimed to determine the proportion, clinical characteristics, hormonal status, median time for normalization of serum thyroxine (FT4) and thyroid-stimulating hormone (TSH) and factors affecting time to thyroid function test (TFT) normalization of neonates born to mothers with maternal hyperthyroidism admitted in our institution.
Methodology:
This was a retrospective cohort study that included 170 newborns admitted to the Neonatal Intensive Care Unit (NICU) of Hospital Universiti Sains Malaysia (HUSM) with a history of maternal hyperthyroidism from January 2013 until December 2018. We analyzed their baseline demographic and clinical characteristics, maternal thyroid status and antibody levels. Finally, we analyzed newborn thyroid function and thyroid antibodies.
Results:
The proportion of neonates born to mothers with maternal hyperthyroidism was 0.8% (170 of 20,198 neonates within the study period). Seven (4.1%) developed overt hyperthyroidism, while four (2.4%) had thyroid storm. The median time for thyroid function test normalization was 30 days (95% CI: 27.1 to 32.8). The median time for TFT normalization was longer among neonates of mothers with positive thyroid antibodies [46.6 days (95% CI, 20.6 to 39.4)] and of mothers who received anti-thyroid treatment [31.7 days (95% CI, 23.5 to 39.9)].
Conclusion
Neonates born to mothers with hyperthyroidism is uncommon. These babies were observed to have a longer time for normalization of thyroid function tests if their mothers had thyroid antibodies or received anti-thyroid treatment.
3.REVIEW - Assessment tools to measure postnatal mental illness: A 10-year scoping review
Siti Roshaidai Mohd Arifin ; Nur Liyana Shahmi Ruslan ; Khadijah Hasanah Abang Abdullah ; Nurul Ain Hidayah Abas ; Rohayah Husain ; Karimah Hanim Abd Aziz ; Ramli Musa ; Fathima Begum Syed Mohideen ; Asma Perveen ; Khairi Che Mat
Malaysian Family Physician 2022;17(2):10-21
Introduction:
The use of assessment tools to measure postnatal mental illness is essential in healthcare settings. However, variations in the types of tools and their reliability in a particular population lead to under-recognition of mental health status in postnatal mothers. The aim of this review is to evaluate the most recent 10 year of research on the validity and reliability of postnatal mental illness assessment tools.
Methods:
A literature search of studies from online databases PubMed, Scopus, and Science Direct was conducted.
Results:
A total of 59 studies were selected for this review. Several studies utilised multiple assessment tools, and a total of 96 assessment tools were identified and classified into six domains: postnatal blues, postnatal stress, postnatal anxiety, postnatal depression, postnatal psychosis, and postnatal psychological disorder. In this review, EPDS was the most common tool used to identify postnatal depression and anxiety while DASS 21 was the most common tool used to identify postnatal psychological disorder. There is a wide range in preponderance of evidence for the reliability of each assessment tool and there were inconsistencies in assessing the validity of the assessment tools.
Conclusion
This review provides information regarding some of the main assessment tools currently available to measure postnatal mental illnesses. There were no standardised tools that were used in a particular setting. The results may differ in different population because there are differences in not only languages and dialects, but also cultural and racial backgrounds, which greatly influences their perception and interpretation of postnatal mental illness.
Mental Disorders
4.A Case Series of Hereditary Congenital Cataract
Nurul Faaiqah Jainuddin ; Azlindarita Aisyah Mohd Abdullah ; Visvaraja Subrayan ; Norlina Ramli ; Nurliza Khaliddin
Malaysian Journal of Medicine and Health Sciences 2020;16(No.2):336-338
Congenital cataract is a major cause of preventable blindness in children. It can be either hereditary or non-hereditary. In this case series, we present three cases of congenital cataract with a strong family history. The grandparents and parents of these patients had cataract diagnosed in late childhood whilst the patients in this case series were diagnosed with congenital cataract earlier. There was no history of consanguineous marriage in any of the families. These cases show that, in the presence of a strong family history, a child will present with congenital cataract earlier in their life. Hence, babies from such families should be screened at birth and at regular intervals within the first year of life to enable early diagnosis and subsequent surgical intervention to reduce the incidence and burden of amblyopia.
5.Morphological characteristics of microfilariae in blood smears of the common treeshrew Tupaia glis (Mammalia: Scandentia) in Gemas, Negeri Sembilan, Malaysia
Mat Udin, A.S. ; Uni, S. ; Zainuri, N.A. ; Abdullah Halim, M.R. ; Belabut, D.A. ; Mohamad Ikbal, N.H. ; Saarani, M.A.F. ; Chen, C.D. ; Uga, S. ; Ramli, R. ; Sofian-Azirun, M.
Tropical Biomedicine 2020;37(No.4):1152-1157
Some filarial nematodes, such as Wuchereria bancrofti, Brugia malayi, and Brugia
timori, cause lymphatic diseases in humans in the tropics, whereas other filarial parasites
from wild animals cause zoonotic diseases in humans worldwide. To elucidate the prevalence
and diversity of filarial parasites in Malaysia, we investigated the filarial parasites from wild
animals in Gemas, Negeri Sembilan. To find adult filarial parasites, we dissected 26 animals,
which included five frogs, one skink, one snake, two birds, six common treeshrews, and 11
rats. Then, we examined microfilariae in the blood smears and skin snips obtained from each
animal. We found two types of microfilariae in the blood smears of common treeshrews: one
was very similar to Malayfilaria sofiani and the other closely resembled Brugia tupaiae.
These findings indicate an additional distribution of these filarial parasites in Gemas.
6.Paediatric asthma clinical pathway: Impact on cost and quality of care
Shakirah Md.Sharif ; Jamalludin Ab Rahman ; Hasniah Abdul Latif ; Rus Anida Awang ; Mariana Daud ; Ahmad Fadzil Abdullah ; Dayang Zuraini Sahadan ; Su Siew Choo ; Ramli Zainal ; Samsinah Hussain ; Norzila Mohamed Zainudin
The Medical Journal of Malaysia 2019;74(2):138-144
INTRODUCTION: Uncontrolled asthma may cause an
increase in healthcare utilisation, hospital admission and
productivity loss. With the increasing burden of asthma in
Malaysia, strategies aimed at reducing cost of care should
be explored. OBJECTIVE: This study aims to determine if a
clinical pathway (CPW) for inpatient paediatric asthma
would reduce average length of stay (ALOS), improve
asthma management and decrease cost.
METHODS: A quasi-experimental, pre-post study was used
to evaluate the CPW effectiveness. Paediatric inpatients
aged 5-18 years old, admitted for acute asthma exacerbation
from September 2015 to April 2016 were prospectively
recruited. Data from patients admitted from January-July
2015 were used as control. CPW training was carried out in
August 2015 using standardised modules. Direct admission
cost from the provider's prospective was calculated.
Outcomes compared were differences in ALOS, discharge
medication, readmission within 28 days of discharge and
cost.
RESULTS: ALOS is 26 hours lower in the CPW group for
severe exacerbations and underlying uncontrolled asthma
(19.2 hours) which is clinically significant as patients have
shorter hospital stay. More newly-diagnosed intermittent
asthmatics were discharged with relievers in the CPW group
(p-value 0.006). None of the patients in the CPW group had
readmissions (p-value 0.16). Mean treatment cost for
patients in the intervention group is higher at RM843.39 (SD
±48.99, versus RM779.21 SD±44.33).
CONCLUSION: This study found that management using a
CPW may benefit asthmatic patients with uncontrolled
asthma admitted with severe exacerbation. Further studies
will be needed to explore CPW's impact on asthma
management starting from the emergency department.
7.Neuroimaging findings are sensitive and specific in diagnosis of tuberculous meningitis
Mei-Ling Sharon Tai ; Hazman Mohd Nor ; Kartini Rahmat ; Shanthi Viswanathan ; Khairul Azmi Abdul Kadir ; Norlisah Ramli ; Fatimah Kamila Abu Bakar ; Norzaini Rose Mohd Zain ; Suhailah Abdullah ; Jun Fai Yap ; Ahmed Shaheed ; Boon Seng Ng ; Mohd Hanip Rafia ; Chong Tin Tan
Neurology Asia 2017;22(1):15-23
Objective: The primary objective of this study was to describe the neuroimaging changes of tuberculous
meningitis (TBM), and to determine the role of neuroimaging in the diagnosis of TBM. Methods:
Between January 2009 and July 2015, we prospectively recruited TBM patients in two hospitals in
Malaysia. Neuroimaging was performed and findings were recorded. The control consists of other types
of meningo-encephalitis seen over the same period. Results: Fifty four TBM patients were recruited.
Leptomeningeal enhancement was seen in 39 (72.2%) patients, commonly at prepontine cistern and
interpeduncular fossa. Hydrocephalus was observed in 38 (70.4%) patients, 25 (46.3%) patients had
moderate and severe hydrocephalus. Thirty four patients (63.0%) had cerebral infarction. Tuberculoma
were seen in 29 (53.7%) patients; 27 (50.0%) patients had classical tuberculoma, 2 (3.7%) patients
had “other” type of tuberculoma, 18 (33.3%) patients had ≥5 tuberculoma, and 11 (20.4%) patients
had < 5 tuberculoma. Fifteen (37.2%) patients had vasculitis, 6 (11.1%) patients had vasospasm. Close
to nine tenth (88.9%) of the patients had ≥1 classical neuroimaging features, 77.8% had ≥ 2 classical
imaging features of TBM (basal enhancement, hydrocephalus, basal ganglia / thalamic infarct, classical
tuberculoma, and vasculitis/vasospasm). Only 4% with other types of meningitis/encephalitis had ≥1
feature, and 1% had two or more classical TBM neuroimaging features. The sensitivity of the imaging
features of the imaging features for diagnosis of TBM was 88.9% and the specificity was 95.6%.
Conclusion: The classic imaging features of basal enhancement, hydrocephalus, basal ganglia/thalamic
infarct, classic tuberculoma, and vasculitis are sensitive and specific to diagnosis of TBM.
Tuberculosis, Meningeal
8.Disrupted-in-Schizophrenia-1 SNPs and Susceptibility to Schizophrenia: Evidence from Malaysia.
A Talib NORLELAWATI ; Abdullah KARTINI ; Kuzaifah NORSIDAH ; Musa RAMLI ; Abdul Razak TARIQ ; Wan Taib WAN ROHANI
Psychiatry Investigation 2015;12(1):103-111
OBJECTIVE: Even though the role of the DICS1 gene as a risk factor for schizophrenia is still unclear, there is substantial evidence from functional and cell biology studies that supports the connection of the gene with schizophrenia. The studies associating the DISC1 gene with schizophrenia in Asian populations are limited to East-Asian populations. Our study examined several DISC1 markers of schizophrenia that were identified in the Caucasian and East-Asian populations in Malaysia and assessed the role of rs2509382, which is located at 11q14.3, the mutual translocation region of the famous DISC1 translocation [t (1; 11) (p42.1; q14.3)]. METHODS: We genotyped eleven single-neucleotide polymorphism (SNPs) within or related to DISC1 (rs821597, rs821616, rs4658971, rs1538979, rs843979, rs2812385, rs1407599, rs4658890, and rs2509382) using the PCR-RFLP methods. RESULTS: In all, there were 575 participants (225 schizophrenic patients and 350 healthy controls) of either Malay or Chinese ethnicity. The case-control analyses found two SNPs that were associated with schizophrenia [rs4658971 (p=0.030; OR=1.43 (1.35-1.99) and rs1538979-(p=0.036; OR=1.35 (1.02-1.80)] and rs2509382-susceptibility among the males schizophrenics [p=0.0082; OR=2.16 (1.22-3.81)]. This is similar to the meta-analysis findings for the Caucasian populations. CONCLUSION: The study supports the notion that the DISC1 gene is a marker of schizophrenia susceptibility and that rs2509382 in the mutual DISC1 translocation region is a susceptibility marker for schizophrenia among males in Malaysia. However, the finding of the study is limited due to possible genetic stratification and the small sample size.
Asian Continental Ancestry Group
;
Case-Control Studies
;
Humans
;
Malaysia*
;
Male
;
Polymorphism, Single Nucleotide*
;
Risk Factors
;
Sample Size
;
Schizophrenia*
9.Primary angiitis of the central nervous system with myelopathy as initial clinical presentation
Cheng Yin Tan ; Ganeshwara Lingam ; Kartini Rahmat ; Suhailah Abdullah ; Ai Huey Tan ; Mei-Ling Sharon Tai ; Norlisah Ramli ; Wong Kum Thong ; Chong Tin Tan
Neurology Asia 2015;20(1):79-84
Primary angiitis of the central nervous system (PACNS) is a rare vasculitis restricted to the central
nervous system without systemic involvement. Delay in diagnosis and treatment is common due to its
non-specific symptoms and lack of non-invasive diagnostic tests. Myelopathy can occur in PACNS,
during the clinical course of the illness, with or without cerebral symptoms. We describe here a 51
year-old ethnic Chinese woman who presented initially with paraparesis without cerebral symptoms.
The diagnosis of PACNS was eventually made from brain biopsy when she subsequently developed
cerebral involvement. Despite aggressive treatment, the patient developed progressive neurological
deterioration and died. This patient demonstrates the rare occurrence of myelopathy as the sole initial
presentation of PACNS.
Central Nervous System
;
Spinal Cord Diseases
10.Ultrasonographic Findings in Eyes with Retinopathy of Prematurity in Malaysia
Lee Kok Foo ; Abdul Rahim Adlina ; Raja Azmi Mohd Noor ; Wan Hazabbah Wan Hitam ; Embong Zunaina ; Abdullah Sarimah ; Noramazlan Ramli ; Zulkifli Abdul Ghani ; Josept Vijaya Alagaratnam ; Jamalia Rahmat ; Sunder Ramasamy ; Ismail Shatriah
The Medical Journal of Malaysia 2013;68(1):39-43
RetCam is an excellent screening tool for the detection of
retinopathy of prematurity (ROP). However, affordability is a barrier when adopting the use of RetCam in developing
countries. We aimed to describe different stages of ROP
using ultrasonographic B-scan and to evaluate the
association between funduscopic examinations and
ultrasonographic B-scan findings in premature neonates
with ROP in Malaysia. A descriptive cross sectional study
was conducted in 90 eyes of 47 premature neonates with
different stages of ROP in three tertiary hospitals in
Malaysia. Experienced ophthalmologists performed detailed
funduscopic examinations using binocular indirect
ophthalmoscopy (BIO). A masked examiner performed a 10
MHz ultrasonographic B-scan evaluation with 12 meridian
position images within 48 hours of clinical diagnosis. Data
from the clinical examination and ultrasonographic findings
were collected and analysed. We recruited 37 eyes (41.1%)
with stage 1 ROP, 29 eyes (32.3%) with stage 2, 18 eyes
(20.0%) with stage 3, and 3 eyes (3.3%) with stages 4 and 5
based on the clinical assessment. Ultrasonography
correctly identified 3 (8.1%) stage 1 eyes, 17 (58.6%) stage 2 eyes, 13 (72.2%) stage 3 eyes, and 3 each (100%) of the stage 4 and 5 eyes. There was a significant association between the funduscopic signs and the ultrasound findings for stage
2 ROP and above (Fisher’s exact test, p <0.001). In
conclusion, all stages of ROP were detected and described
with a 10 MHz ultrasonic B-scan system. A significant
association was observed between funduscopic signs and
ultrasonographic findings in premature Malaysian neonates
with stage 2 ROP and above.


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