1.Preparation of Pooled Sera by Using Stirrer.
Journal of Laboratory Medicine and Quality Assurance 2009;31(1):183-186
BACKGROUND: The aim of this study was to compare a new stir method with the conventional refrozen method used to prepare pooled sera. METHODS: We prepared fifteen different pooled sera by using two pooled sera preparation methods. Twenty dispensed sera from each pooled serum were analyzed for glucose, total protein, albumin, aspartate aminotransferase, total bilirubin, triglyceride, blood urea nitrogen, creatinine, sodium, potassium, and chloride concentrations. For stability study, six different pooled sera were stored at room temperature, 4degrees C, and -70degrees C for 3 months and the eleven components were measured for each month. RESULTS: There was no difference in homogeneity between stir and refrozen pooled sera preparation methods and good stability was observed for -70degrees C storage of all measured components. CONCLUSIONS: The stir method might be more useful than refrozen method to prepare pooled sera.
Aspartate Aminotransferases
;
Bilirubin
;
Blood Urea Nitrogen
;
Creatinine
;
Glucose
;
Potassium
;
Quality Control
;
Sodium
2.Efficacy of Intravitreal Anti-vascular Endothelial Growth Factor or Steroid Injection in Diabetic Macular Edema According to Fluid Turbidity in Optical Coherence Tomography.
Kyungmin LEE ; Heeyoung CHUNG ; Youngsuk PARK ; Joonhong SOHN
Korean Journal of Ophthalmology 2014;28(4):298-305
PURPOSE: To determine if short term effects of intravitreal anti-vascular endothelial growth factor or steroid injection are correlated with fluid turbidity, as detected by spectral domain optical coherence tomography (SD-OCT) in diabetic macular edema (DME) patients. METHODS: A total of 583 medical records were reviewed and 104 cases were enrolled. Sixty eyes received a single intravitreal bevacizumab injection (IVB) on the first attack of DME and 44 eyes received triamcinolone acetonide treatment (IVTA). Intraretinal fluid turbidity in DME patients was estimated with initialintravitreal SD-OCT and analyzed with color histograms from a Photoshop program. Central macular thickness and visual acuity using a logarithm from the minimum angle of resolution chart, were assessed at the initial period and 2 months after injections. RESULTS: Visual acuity and central macular thickness improved after injections in both groups. In the IVB group, visual acuity and central macular thickness changed less as the intraretinal fluid became more turbid. In the IVTA group, visual acuity underwent less change while central macular thickness had a greater reduction (r = -0.675, p = 0.001) as the intraretinal fluid was more turbid. CONCLUSIONS: IVB and IVTA injections were effective in reducing central macular thickness and improving visual acuity in DME patients. Further, fluid turbidity, which was detected by SD-OCT may be one of the indexes that highlight the influence of the steroid-dependent pathogenetic mechanism.
Aged
;
Angiogenesis Inhibitors/*therapeutic use
;
Bevacizumab/*therapeutic use
;
Diabetic Retinopathy/*drug therapy/physiopathology
;
Female
;
Glucocorticoids/*therapeutic use
;
Humans
;
Intravitreal Injections
;
Macular Edema/*drug therapy/physiopathology
;
Male
;
Middle Aged
;
Nephelometry and Turbidimetry
;
Retina/pathology
;
*Subretinal Fluid
;
Tomography, Optical Coherence
;
Treatment Outcome
;
Triamcinolone Acetonide/*therapeutic use
;
Vascular Endothelial Growth Factor A/antagonists & inhibitors
;
Visual Acuity/physiology
3.Single-color Multitarget Flow Cytometry Using Monoclonal Antibodies Labeled with Different Intensities of the Same Fluorochrome.
Annals of Laboratory Medicine 2012;32(3):171-176
BACKGROUND: We developed a single-color multitarget flow cytometry (SM-FC) assay, a single-tube assay with graded mean fluorescence intensities (MFIs). We evaluated the repeatability of SM-FC, and its correlation with multicolor flow cytometry (MFC), to assess its application as a routine FC assay. METHODS: We selected CD19, CD3, CD4, and CD8 as antigen targets to analyze a lymphocyte subset. MFIs were graded by adjusting monoclonal antibody (mAb) volumes to detect several cell populations. Dimly labeled mAb was prepared by decreasing mAb volume and the optimum diluted volume was determined by serial dilution. SM-FC repeatability was analyzed 10 times in 2 normal controls. The correlation between SM-FC and MFC was evaluated in 20 normal and 23 patient samples. RESULTS: CV values (0.8-5.0% and 1.3-4.1% in samples 1 and 2, respectively) acquired by SM-FC with CD3-fluorescein alpha-isothyocyanate (FITC)dim+CD4-FITCbright and with CD19-FITCdim+CD3-FITCbright showed good repeatability, comparable to that acquired by MFC (1.6-3.7% and 1.0-4.8% in samples 1 and 2, respectively). Excellent correlation was observed between the 2 methods in the 20 normal samples (B cells, T cells, non-Thelper cells, and Thelper cells; r2=0.87, 0.97, 0.97, and 0.98, respectively; P<0.05). There were also linear relationships between SM-FC with CD19-FITCdim+CD3-FITCbright and CD8-PEdim+CD4-PEbright, and MFC, in the 23 patient samples (B cells, T cells, Tcytotoxic cells, and Thelper cells; r2> or =0.98, 0.99, 0.99, and 0.99, respectively; P<0.05). CONCLUSIONS: The multicolor, single-tube SM-FC technique is a potential alternative tool for identifying a lymphocyte subset.
Antibodies, Monoclonal/chemistry/*immunology
;
Antigens, CD19/chemistry/metabolism
;
Antigens, CD3/chemistry/metabolism
;
Antigens, CD4/chemistry/metabolism
;
Antigens, CD8/chemistry/metabolism
;
B-Lymphocyte Subsets/immunology/metabolism
;
Color
;
Flow Cytometry/*methods
;
Fluorescein-5-isothiocyanate/*chemistry
;
Humans
;
T-Lymphocyte Subsets/immunology/metabolism
4.Incidental Identification of Plasmodium vivax During Routine Complete Blood Count Analysis Using the UniCel DxH 800.
Soyoung SHIN ; Sun Hee PARK ; Joonhong PARK
Annals of Laboratory Medicine 2018;38(2):165-168
No abstract available.
Blood Cell Count*
;
Plasmodium vivax*
;
Plasmodium*
5.Assessment of the Quantitative Ability of AdvanSure TB/NTM Real-Time PCR in Respiratory Specimens by Comparison with Phenotypic Methods.
Hyeyoung LEE ; Kang Gyun PARK ; Gundong LEE ; Joonhong PARK ; Yong Gyu PARK ; Yeon Joon PARK
Annals of Laboratory Medicine 2014;34(1):51-55
Accurate quantification of mycobacterial load is important to evaluate disease severity and to monitor the course of treatment in tuberculosis (TB). We evaluated the quantitative capability of the AdvanSure TB/NTM real-time PCR kit (LG Life Science, Korea) to determine the cycle threshold (Ct) for mycobacterial burden. We retrospectively analyzed data from 108 patients whose respiratory specimens (sputums and bronchoalveolar lavage fluids) were positive for Mycobacterium tuberculosis complex (85 culture-positive and 23 culture-negative specimens). We compared Ct values with grades of acid-fast bacilli (AFB) staining, semi-quantitative colony count on solid medium, and time to positivity (TTP) in liquid and solid media. We also investigated the cutoff Ct value for predicting stain-positive status. Ct value showed significant reverse correlation with AFB staining grade (r(s)=-0.635, P<0.01). Ct value significantly decreased as the semi-quantitative counts on the solid medium increased (P<0.001), and the mean Ct value of each of the groups 1+, 2+, 3+, and 4+ were 29.0, 30.0, 27.1, and 25.5, respectively. A weak correlation between Ct value and TTP in liquid and solid media was observed (r(s)=0.468 and 0.365, respectively). A cutoff Ct value of <33.2 best predicted stain positivity, with a sensitivity of 95.0% and a specificity of 32.0%. Our findings suggest the potential use of AdvanSure TB/NTM real-time PCR kit for quantitatively determining bacterial burden, albeit with some enhancements.
Area Under Curve
;
Bronchoalveolar Lavage Fluid/microbiology
;
DNA, Bacterial/*analysis
;
Humans
;
Mycobacterium tuberculosis/genetics/*isolation & purification
;
Phenotype
;
ROC Curve
;
Reagent Kits, Diagnostic
;
*Real-Time Polymerase Chain Reaction
;
Retrospective Studies
;
Sensitivity and Specificity
;
Sputum/microbiology
;
Tuberculosis/diagnosis/microbiology
6.The Effects of Peroxisome Proliferator Activated Receptor alpha (PPARalpha) Activator on Patients with Facial Erythema.
Yeseul KIM ; Youlee JUNG ; Jongkyung YOUM ; Joonhong PARK ; You In BAE ; Younglip PARK ; Sanghoon LEE
Korean Journal of Dermatology 2014;52(9):608-614
BACKGROUND: Long-term use of topical steroids for inflammatory skin diseases can induce complications, and efforts to find a better treatment are being continued. Peroxisome proliferator activated receptor alpha (PPARalpha) suppresses the skin's inflammatory reaction, maintains the homeostasis of the skin, and plays an important role in skin barrier function. OBJECTIVE: This study analyzed the effects of a skin moisturizer containing PPARalpha activator on various inflammatory skin diseases causing facial erythema and evaluated the observed improvements. METHODS: The PPARa activator used for this study is composed of supercritical extracts from Euryale ferox, Euphorbia lathyris, and Rosa multiflora, which showed significant effects in the transactivation assay compared to Wy14643. Moisturizer containing PPARalpha was applied to the faces of 31 patients with symmetric facial erythema, with PPARalpha applied on one-half of the face and a control moisturizer on the other half of the face twice a day for 2 weeks. The percentage of erythema index, erythema index, skin hydration, and transepidermal water loss was checked to evaluate treatment effect. Both patients and clinicians each assessed the improvement of erythema on both sides of a patient's face. RESULTS: Moisturizer containing PPARalpha agonist significantly improved erythema index measured with Mexameter MX18(R) and percentage of erythema index by polarization color imaging system (DermaVision-PRO(R)) (p<0.05). However, there was no significant improvement in skin hydration and transepidermal water loss. Improvement of erythema was also shown on both the patient and clinician graded assessments. CONCLUSION: Topical PPARalpha agonist applied during clinical practice was relatively safe and effective. This can be applied clinically to various inflammatory skin diseases causing erythema.
Erythema*
;
Euphorbia
;
Homeostasis
;
Humans
;
PPAR alpha*
;
Rosa
;
Skin
;
Skin Diseases
;
Steroids
;
Transcriptional Activation
7.Molecular Analysis of Two Cases of Severe Congenital Neutropenia.
Joonhong PARK ; Myungshin KIM ; Jihyang LIM ; Yonggoo KIM ; Bin CHO ; Yeon Joon PARK ; Kyungja HAN
The Korean Journal of Laboratory Medicine 2010;30(2):111-116
Severe congenital neutropenia is a rare hematological disease characterized by a selective decrease in circulating neutrophils, maturation arrest of granulocytic precursors at the promyelocyte stage, and recurrence of infections. A 2-month-old male infant (patient A) and a 14-month-old female child (patient B) were referred to our hospital due to severe neutropenia. Sequencing analysis of ELA2 and HAX1 genes was performed. Two single nucleotide polymorphisms of HAX1 gene were found. They were 5,104T-->G point mutation of exon 1 and 5,474A-->G point mutation of intron 1 in HAX1 gene. The mutation of ELA2 gene was not found. The patient A showed a good response to granulocyte colony-stimulating factor (G-CSF) treatment and the absolute neutrophil count recovered to 1,195/microliter. But the patient B showed a partial response to G-CSF treatment and experienced several episodes of herpetic gingivostomatitis, oral ulcer, acute pharyngotonsillitis and otitis media during follow-up.
Adaptor Proteins, Signal Transducing/genetics
;
Bone Marrow/pathology
;
Female
;
Granulocyte Colony Stimulating Factor, Recombinant/adverse effects/therapeutic use
;
Humans
;
Infant
;
Male
;
Neutropenia/congenital/drug therapy/*genetics
;
Neutrophils/cytology/pathology
;
Oral Ulcer/etiology
;
Otitis Media/etiology
;
Polymorphism, Single Nucleotide
;
Serine Endopeptidases/genetics
;
Stomatitis, Herpetic/etiology
8.Determining Genotypic Drug Resistance by Ion Semiconductor Sequencing With the Ion AmpliSeq™ TB Panel in Multidrug-Resistant Mycobacterium tuberculosis Isolates.
Joonhong PARK ; So Youn SHIN ; Kyungjong KIM ; Kuhn PARK ; Soyoung SHIN ; Chunhwa IHM
Annals of Laboratory Medicine 2018;38(4):316-323
BACKGROUND: We examined the feasibility of a full-length gene analysis for the drug resistance-related genes inhA, katG, rpoB, pncA, rpsL, embB, eis, and gyrA using ion semiconductor next-generation sequencing (NGS) and compared the results with those obtained from conventional phenotypic drug susceptibility testing (DST) in multidrug-resistant Mycobacterium tuberculosis (MDR-TB) isolates. METHODS: We extracted genomic DNA from 30 pure MDR-TB isolates with antibiotic susceptibility profiles confirmed by phenotypic DST for isoniazid (INH), rifampin (RIF), ethambutol (EMB), pyrazinamide (PZA), amikacin (AMK), kanamycin (KM), streptomycin (SM), and fluoroquinolones (FQs) including ofloxacin, moxifloxacin, and levofloxacin. Enriched ion spheres were loaded onto Ion PI Chip v3, with 30 samples on a chip per sequencing run, and Ion Torrent sequencing was conducted using the Ion AmpliSeq TB panel (Life Technologies, USA). RESULTS: The genotypic DST results revealed good agreement with the phenotypic DST results for EMB (Kappa 0.8), PZA (0.734), SM (0.769), and FQ (0.783). Agreements for INH, RIF, and AMK+KM were not estimated because all isolates were phenotypically resistant to INH and RIF, and all isolates were phenotypically and genotypically susceptible to AMK+KM. Moreover, 17 novel variants were identified: six (p.Gly169Ser, p.Ala256Thr, p.Ser383Pro, p.Gln439Arg, p.Tyr597Cys, p.Thr625Ala) in katG, one (p.Tyr113Phe) in inhA, five (p.Val170Phe, p.Thr400Ala, p.Met434Val, p.Glu812Gly, p.Phe971Leu) in rpoB, two (p.Tyr319Asp and p.His1002Arg) in embB, and three (p.Cys14Gly, p.Asp63Ala, p.Gly162Ser) in pncA. CONCLUSIONS: Ion semiconductor NGS could detect reported and novel amino acid changes in full coding regions of eight drug resistance-related genes. However, genotypic DST should be complemented and validated by phenotypic DSTs.
Amikacin
;
Clinical Coding
;
Complement System Proteins
;
DNA
;
Drug Resistance*
;
Ethambutol
;
Fluoroquinolones
;
Isoniazid
;
Kanamycin
;
Levofloxacin
;
Mycobacterium tuberculosis*
;
Mycobacterium*
;
Ofloxacin
;
Pyrazinamide
;
Rifampin
;
Semiconductors*
;
Streptomycin
9.Circulating Respiratory Syncytial Virus Genotypes and Genetic Variability of the G Gene during 2017 and 2018/2019 Seasonal Epidemics Isolated from Children with Lower Respiratory Tract Infections in Daejeon, Korea
Hyun Mi KANG ; Ki Cheol PARK ; Joonhong PARK ; Hong Ryang KIL ; Eun Ae YANG
Journal of Korean Medical Science 2020;35(49):e422-
Background:
Respiratory syncytial virus (RSV) is a major pathogen causing respiratory tract infections in infants and young children. The aim of this study was to confirm the genetic evolution of RSV causing respiratory infections in children at Daejeon in Korea, through G gene analysis of RSV-A and RSV-B strains that were prevalent from 2017 to 2019.
Methods:
Pediatric patients admitted for lower respiratory tract infections at The Catholic University of Korea Daejeon St. Mary's Hospital in the 2017 and 2018/2019 RSV seasonal epidemics, who had RSV detected via multiplex polymerase chain reaction (PCR) were included. The nucleic acid containing RSV-RNA isolated from each of the patients' nasal discharge during standard multiplex PCR testing was stored. The G gene was sequenced and phylogenetic analysis was performed using MEGA X program and the genotype was confirmed.
Results:
A total of 155 specimens including 49 specimens from 2017 and 106 specimens from 2018-2019 were tested. The genotype was confirmed in 18 specimens (RSV-A:RSV-B = 4:14) from 2017 and 8 specimens (RSV-A:RSV-B = 7:1) from 2018/2019. In the phylogenetic analysis, all RSV-A type showed ON1 genotype and RSV-B showed BA9 genotype.
Conclusion
RSV-B belonging to BA9 in 2017, and RSV-A belonging to ON1 genotype in 2018/2019 was the most prevalent circulating genotypes during the two RSV seasons in Daejeon, Korea.
10.X-Linked Spondyloepiphyseal Dysplasia Tarda: Identification of a TRAPPC2 Mutation in a Korean Pedigree.
Hyejin RYU ; Joonhong PARK ; Hyojin CHAE ; Myungshin KIM ; Yonggoo KIM ; In Young OK
Annals of Laboratory Medicine 2012;32(3):234-237
Spondyloepiphyseal dysplasia (SED) comprises a heterogeneous group of skeletal dysplasias that primarily affect the epiphyses and vertebral bodies. Patients affected by SED usually exhibit short stature and experience early development of degenerative osteoarthritis. SED is subdivided into congenita and tarda forms according to the age at onset and clinical severity, and further subdivided into genetically different forms according to the mode of inheritance and the gene involved. We report a 14-yr-old Korean male who presented with a disproportionately short stature and a short trunk. A pedigree analysis of 3 generations with 6 affected persons revealed an X-linked recessive mode of inheritance. Mutation analysis of the TRAPPC2 (previously called SEDL) gene, the only gene associated with X-linked spondyloepiphyseal dysplasia tarda (X-linked SEDT; MIM 313400), was performed, and a splice-donor site mutation in intron 3 of the TRAPPC2 gene (c.93+5G>A) was identified in the proband and in his unaffected mother (a heterozygote). This mutation is one of the 2 most frequent mutations reported in the medical literature, and is known to result in exon 3 skipping. This is the first report of a genetically confirmed X-linked SEDT case in Korea and highlights the importance of recognizing the mode of inheritance in the diagnosis of X-linked SEDT.
Adolescent
;
Asian Continental Ancestry Group/*genetics
;
DNA Mutational Analysis
;
Exons
;
Genetic Diseases, X-Linked/*genetics
;
Humans
;
Male
;
Membrane Transport Proteins/*genetics
;
Osteochondrodysplasias/*genetics/radiography
;
Pedigree
;
Republic of Korea
;
Transcription Factors/*genetics