1.Clinical Significance of Fecal Lactoferrin and Multiplex Polymerase Chain Reaction in Patients with Acute Diarrhea.
Hae Mi LEE ; Seungok LEE ; Bo In LEE ; Dong Wook JEKARL ; Joo Yong SONG ; Hye Jung CHOI ; Bong Koo KANG ; Eun Joo IM ; Joon Sung KIM ; Jong In KIM ; Byung Wook KIM ; Hwang CHOI
Gut and Liver 2015;9(5):636-640
BACKGROUND/AIMS: The diagnostic yield of fecal leukocyte and stool cultures is unsatisfactory in patients with acute diarrhea. This study was performed to evaluate the clinical significance of the fecal lactoferrin test and fecal multiplex polymerase chain reaction (PCR) in patients with acute diarrhea. METHODS: Clinical parameters and laboratory findings, including fecal leukocytes, fecal lactoferrin, stool cultures and stool multiplex PCR for bacteria and viruses, were evaluated prospectively for patients who were hospitalized due to acute diarrhea. RESULTS: A total of 54 patients were included (male, 23; median age, 42.5 years). Fecal leukocytes and fecal lactoferrin were positive in 33 (61.1%) and 14 (25.4%) patients, respectively. Among the 31 patients who were available for fecal pathogen evaluation, fecal multiplex PCR detected bacterial pathogens in 21 patients, whereas conventional stool cultures were positive in only one patient (67.7% vs 3.2%, p=0.000). Positive fecal lactoferrin was associated with presence of moderate to severe dehydration and detection of bacterial pathogens by multiplex PCR (21.4% vs 2.5%, p=0.049; 100% vs 56.5%, p=0.032, respectively). CONCLUSIONS: Fecal lactoferrin is a useful marker for more severe dehydration and bacterial etiology in patients with acute diarrhea. Fecal multiplex PCR can detect more causative organisms than conventional stool cultures in patients with acute diarrhea.
Adult
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Biomarkers/analysis
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Dehydration/enzymology/microbiology
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Diarrhea/complications/*enzymology/microbiology
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Feces/*enzymology/microbiology
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Female
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Humans
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Lactoferrin/*analysis
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Male
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Multiplex Polymerase Chain Reaction/*statistics & numerical data
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Prospective Studies
2.Prenatal development of human major salivary glands. Histological and immunohistochemical characteristics with reference to adult and neoplastic salivary glands.
Journal of Korean Medical Science 1996;11(3):203-216
No abstract available.
Actins/analysis
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Adult
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Female
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Human
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Immunohistochemistry
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Lactoferrin/analysis
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Muramidase/analysis
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Phosphopyruvate Hydratase/metabolism
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Pregnancy
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S100 Proteins/analysis
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Salivary Gland Neoplasms/chemistry/*pathology
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Salivary Glands/chemistry/*embryology
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Submandibular Gland/embryology
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alpha 1-Antitrypsin/analysis
3.Identification of UVB Effects on Gene Expressed by Normal Human Melanocytes.
Hyoung Seob KIM ; Hyun Ho PARK ; Mu Hyoung LEE
Korean Journal of Dermatology 2003;41(12):1597-1602
BACKGROUND: Irradiation of the skin with ultraviolet rays result in alterations of immune response as well as melanogenesis and melanocarcinogenensis. These effects are largely mediated by soluble mediators released from epidermal cells in response to ultraviolet rays. OBJECTIVE: To evaluate the effect of ultraviolet B (UVB) irradiation on the normal human melanocyte gene expression. METHODS: We demonstrated genes modulated by UVB irradiation among over 300 genes coding CDs, cytokins, growth factors, and growth factor receptors in normal human melanocytes by cDNA microarray technique. RESULTS: Two genes out of 384 genes in cultured normal human melanocytes were found up-regulated following UVB irradiation. They are the genes coding lactotransferrin and CD160. Forty one genes out of 384 genes were found down-regulated by UVB irradiation. They included the genes coding IL-9, IL-5, TNF-alpha, TNF-beta, IL-6 receptor and CD20. CONCLUSION: These results provide the basis for future studies on the immunologic role in modulated genes by UV-stressed human melanocytes.
Clinical Coding
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Gene Expression
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Humans*
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Intercellular Signaling Peptides and Proteins
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Interleukin-5
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Interleukin-9
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Lactoferrin
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Lymphotoxin-alpha
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Melanocytes*
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Oligonucleotide Array Sequence Analysis
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Receptors, Growth Factor
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Receptors, Interleukin-6
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Skin
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Tumor Necrosis Factor-alpha
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Ultraviolet Rays
4.The stress of weaning influences serum levels of acute-phase proteins, iron-binding proteins, inflammatory cytokines, cortisol, and leukocyte subsets in Holstein calves.
Myung Hoo KIM ; Ji Young YANG ; Santi Devi UPADHAYA ; Hyun Jun LEE ; Cheol Heui YUN ; Jong K HA
Journal of Veterinary Science 2011;12(2):151-157
The purpose of our study was to investigate changes in immunological parameters induced by weaning stress (including milk restriction) in calves. Fifteen Holstein calves were subjected to weaning at 6 weeks of age. Blood samples were collected at -14, -7, -2, 1, 3, and 5 days post-weaning (DPW; 0 DPW = 42 days). Weaning caused significant (p < 0.01) increases in the neutrophil (NE):lymphocyte (LY) ratio at 5 DPW with a significant (p < 0.05) reduction of LYs. The concentration of acute-phase proteins (haptoglobin and serum amyloid A) also increased significantly (p < 0.05) at 3 and 5 DPW compared to -2 DPW. Levels of the iron-binding protein lactoferrin decreased significantly (p < 0.05) after weaning. Serum tumor necrosis factor-alpha and cortisol levels were elevated (p < 0.05) at 3 DPW, while those of serum interferon-gamma decreased (p < 0.05) at 1 and 3 DPW compared to levels observed before weaning. Weaning significantly (p < 0.05) decreased the percentage of CD25+ T cells in the peripheral blood. In conclusion, weaning stress affected the NE:LY ratio along with the levels of acute phase proteins, lactoferrin, cortisol, and inflammatory cytokines in the peripheral blood of calves. Weaning stress may induce an acute phase response possibly through the elevation of cortisol production and modulation of inflammatory cytokines.
Acute-Phase Proteins/*immunology/metabolism
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Acute-Phase Reaction/immunology/*veterinary
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Animals
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Cattle/*immunology
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Female
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Flow Cytometry
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Haptoglobins/analysis/immunology
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Hydrocortisone/blood/immunology
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Interferon-gamma/blood/immunology
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Lactoferrin/analysis/immunology
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Leukocyte Count/veterinary
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Leukocytes/cytology/*immunology
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Male
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Serum Amyloid A Protein/analysis/immunology
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Stress, Physiological/*physiology
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Tumor Necrosis Factor-alpha/blood/immunology
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Weaning