1.Prognostic Value of Alpha-Fetoprotein in Patients Who Achieve a Complete Response to Transarterial Chemoembolization for Hepatocellular Carcinoma
Jae Seung LEE ; Young Eun CHON ; Beom Kyung KIM ; Jun Yong PARK ; Do Young KIM ; Sang Hoon AHN ; Kwang-Hyub HAN ; Wonseok KANG ; Moon Seok CHOI ; Geum-Youn GWAK ; Yong-Han PAIK ; Joon Hyeok LEE ; Kwang Cheol KOH ; Seung Woon PAIK ; Hwi Young KIM ; Tae Hun KIM ; Kwon YOO ; Yeonjung HA ; Mi Na KIM ; Joo Ho LEE ; Seong Gyu HWANG ; Soon Sun KIM ; Hyo Jung CHO ; Jae Youn CHEONG ; Sung Won CHO ; Seung Ha PARK ; Nae-Yun HEO ; Young Mi HONG ; Ki Tae YOON ; Mong CHO ; Jung Gil PARK ; Min Kyu KANG ; Soo Young PARK ; Young Oh KWEON ; Won Young TAK ; Se Young JANG ; Dong Hyun SINN ; Seung Up KIM ;
Yonsei Medical Journal 2021;62(1):12-20
		                        		
		                        			 Purpose:
		                        			Alpha-fetoprotein (AFP) is a prognostic marker for hepatocellular carcinoma (HCC). We investigated the prognostic value of AFP levels in patients who achieved complete response (CR) to transarterial chemoembolization (TACE) for HCC. 
		                        		
		                        			Materials and Methods:
		                        			Between 2005 and 2018, 890 patients with HCC who achieved a CR to TACE were recruited. An AFP responder was defined as a patient who showed elevated levels of AFP (>10 ng/mL) during TACE, but showed normalization or a >50% reduction in AFP levels after achieving a CR. 
		                        		
		                        			Results:
		                        			Among the recruited patients, 569 (63.9%) with naïve HCC and 321 (36.1%) with recurrent HCC after complete resection were treated. Before TACE, 305 (34.3%) patients had multiple tumors, 219 (24.6%) had a maximal tumor size >3 cm, and 22 (2.5%) had portal vein tumor thrombosis. The median AFP level after achieving a CR was 6.36 ng/mL. After a CR, 473 (53.1%) patients experienced recurrence, and 417 (46.9%) died [median progression-free survival (PFS) and overall survival (OS) of 16.3 and 62.8 months, respectively]. High AFP levels at CR (>20 ng/mL) were independently associated with a shorter PFS [hazard ratio (HR)=1.403] and OS (HR=1.284), together with tumor multiplicity at TACE (HR=1.518 and 1.666, respectively). AFP non-responders at CR (76.2%, n=359 of 471) showed a shorter PFS (median 10.5 months vs. 15.5 months, HR=1.375) and OS (median 41.4 months vs. 61.8 months, HR=1.424) than AFP responders (all p=0.001). 
		                        		
		                        			Conclusion
		                        			High AFP levels and AFP non-responders were independently associated with poor outcomes after TACE. AFP holds clinical implications for detailed risk stratification upon achieving a CR after TACE. 
		                        		
		                        		
		                        		
		                        	
2.Topical Tacrolimus for the Treatment of Atopic Dermatitis with Truncal Lesion.
Hyun Chang KO ; Woo Il KIM ; Sang Hyun CHO ; Young Lip PARK ; Eung Ho CHOI ; Sang Wook SON ; Bark Lynn LEW ; Yang Won LEE ; Young Jun SEO ; Gyong Moon KIM ; Joon Hong MIN ; Chan Ho NA ; Chong Hyun WON ; Hyoseung SHIN ; Kwang Hoon LEE ; Joo Young ROH ; Young Min PARK ; Yong Hyun JANG ; Seok Kweon YUN ; You Chan KIM ; Gyeong Hun PARK ; Chun Wook PARK
Annals of Dermatology 2018;30(2):173-178
		                        		
		                        			
		                        			BACKGROUND: Topical tacrolimus is an effective anti-inflammatory therapy for acute and chronic states of atopic dermatitis (AD) in both adults and children. Topical tacrolimus has particular use at sensitive areas such as the face, anogenitals, and skin folds of neck and extremities. However, many AD patients also experience aggravated symptoms on trunk. OBJECTIVE: The aim of this study was to investigate the efficacy and safety of topical tacrolimus for AD patients with truncal lesions. METHODS: AD patients with truncal lesions who were aged ≥2 years were recruited from 20 centres in Korea. They received treatment with topical tacrolimus ointment twice daily during 4 weeks. The primary end point was change of the local eczema area and severity index (EASI) of the trunk from baseline to day 28. The secondary end points were changes in the patient global assessment (PGA) score and itch visual analogue scale (VAS) score of the trunk between baseline and day 28. RESULTS: Two hundred and ninety-one patients were recruited, and 176 patients completed the full 4-week treatment course. By the end of the treatment, the mean local EASI of the trunk (2.2±4.71) was significantly decreased from that at baseline (4.71±4.03, p < 0.001). PGA (1.71±1.15) and itch VAS score of the trunk (2.61±2.19) on day 28 were also profoundly decreased compared with the baseline (2.96±1.07 and 5.15±2.47, respectively). No serious adverse events were observed during the study period. CONCLUSION: Topical tacrolimus is an effective and safe therapy for truncal lesions in AD patients.
		                        		
		                        		
		                        		
		                        			Administration, Topical
		                        			;
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Dermatitis, Atopic*
		                        			;
		                        		
		                        			Eczema
		                        			;
		                        		
		                        			Extremities
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Neck
		                        			;
		                        		
		                        			Skin
		                        			;
		                        		
		                        			Tacrolimus*
		                        			
		                        		
		                        	
3.Experience with a Simulation Drill for Novel Influenza A (H1N1).
Dongsuk LEE ; Eun Suk PARK ; Mee Kweon OH ; Hyang Suk KIM ; Jeong Yeon PARK ; Shin Ok KOH ; Min Hong JWA ; In Cheol PARK ; Kyeong Ae KIM ; Kyeong Hwan OH ; Chang Oh KIM ; Sang Hun HAN ; Jun Yong CHOI ; June Myung KIM ; Ju Hyun LEE ; Eun Jin HA ; Dong Soo KIM ; Dongsik BANG ; Kyungwon LEE
Korean Journal of Nosocomial Infection Control 2010;15(2):103-111
		                        		
		                        			
		                        			BACKGROUND: It is important that hospitals conduct disaster drills to ensure prompt response in case of a pandemic and thereby prevent a biological disaster. METHODS: In a university hospital of Seoul, a drill was arranged by the members of the drill preparation team who were a part of the response team for infection control of novel influenza A (H1N1). The drill preparation team designed the scenario for the drill, made plans to resolve the potential problems that could occur during that scenario, and organized a survey team and a survey methodology. The scenario consisted of 2 modules: (1) for an intensive care unit and (2) for an emergency care center. The surveyors and field participants were evaluated after the drill exercise. RESULTS: This drill was conducted to improve the response to outbreaks of new infectious diseases. The drill event showed that the communication among the members responsible for the infection control was effective. However, the drill revealed certain drawbacks in the process; this drawbacks involved availability of adequate quarantine space, education on using personal protective equipments, assignment of medical and nonmedical staff, management of visitors, and installment of air-conditioners, heaters, and ventilation units in the areas with H1N1 outbreak. CONCLUSION: This drill helped to improve the process of infection control and overcome the drawbacks in the current process, and thereby helped in achieving positive outcome during the actual pandemic situation when the number of hospital visits and admissions because of H1N1 pandemic had rapidly increased. Although disaster plans and drills are not actively performed, the drill for infection control is essential because the risk for an outbreak of a new infectious disease is increasing.
		                        		
		                        		
		                        		
		                        			Communicable Diseases
		                        			;
		                        		
		                        			Surveys and Questionnaires
		                        			;
		                        		
		                        			Dietary Sucrose
		                        			;
		                        		
		                        			Disasters
		                        			;
		                        		
		                        			Disease Outbreaks
		                        			;
		                        		
		                        			Emergency Medical Services
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Infection Control
		                        			;
		                        		
		                        			Influenza, Human
		                        			;
		                        		
		                        			Intensive Care Units
		                        			;
		                        		
		                        			Mandrillus
		                        			;
		                        		
		                        			Pandemics
		                        			;
		                        		
		                        			Quarantine
		                        			;
		                        		
		                        			Ventilation
		                        			
		                        		
		                        	
4.Development and evaluation of indirect ELISA for the detection of antibodies against Japanese encephalitis virus in swine.
Dong Kun YANG ; Byoung Han KIM ; Seong In LIM ; Jun Hun KWON ; Kyung Woo LEE ; Cheong Up CHOI ; Chang Hee KWEON
Journal of Veterinary Science 2006;7(3):271-275
		                        		
		                        			
		                        			The Japanese encephalitis virus (JEV) is one of causative agents of reproductive failure in pregnant sows. An indirect enzyme-linked immunosorbent assay (I-ELISA) was examined for its potential use in the rapid monitoring of the JEV, and the results were compared with those from the hemagglutination inhibition (HI) and serum neutralization (SN) tests. The comparative analysis showed that the results of I-ELISA showed a significant correlation with the conventional HI (r = 0.867) and SN tests (r = 0.804), respectively. When the I-ELISA results were compared with the traditional diagnostic assays, the sensitivity of the I-ELISA was 94.3% with the HI test and 93.7% with the SN test, respectively. The specificity was found to be 81.4% and 80.0% with the HI and SN tests, respectively. To determine the applicability of I-ELISA in the field, the serum samples from 720 pigs were collected from 4 regions in Korea between July and August 2004. The results indicated that 21.7% of screened pigs were seropositive for the JEV. The seropositive rates of JEV in the 4 provinces were 12.6% in Gyeonggi, 45.0% in Gyeongnam, 16.7% in Jeonbuk, and 12.2% in Jeju. The I-ELISA methodology developed in this study was shown to have considerable sensitivity and specificity through a comparison with HI and the SN tests. Therefore, it might be one of convenient methods for screening a large number of samples in various fields.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antibodies, Viral/blood
		                        			;
		                        		
		                        			Antigens, Viral/immunology
		                        			;
		                        		
		                        			Encephalitis Virus, Japanese/immunology/*isolation&purification
		                        			;
		                        		
		                        			Encephalitis, Japanese/blood/immunology/*veterinary/virology
		                        			;
		                        		
		                        			Enzyme-Linked Immunosorbent Assay/methods/*veterinary
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Hemagglutination Inhibition Tests/veterinary
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Neutralization Tests/veterinary
		                        			;
		                        		
		                        			Swine
		                        			;
		                        		
		                        			Swine Diseases/blood/immunology/*virology
		                        			
		                        		
		                        	
5.Apoptosis in Vero cells infected with Akabane, Aino and Chuzan virus.
Seong In LIM ; Chang Hee KWEON ; Dong Kun YANG ; Dong Seob TARK ; Jun Hun KWEON
Journal of Veterinary Science 2005;6(3):251-254
		                        		
		                        			
		                        			Akabane, Aino and Chuzan virus are arthropod-borne (arbo)viruses mainly associated with reproductive failures in cattle. We investigated apoptosis in Vero cells (C-1586) infected with Akabane, Aino and Chuzan virus. The fragmentation of chromosomal DNA was simultaneously detected with the progress of cytopathic effect from 48 hr to 72 hr post infection, depending on viruses. Although the treatment of cycloheximide blocked apoptosis in Vero cells infected with three viruses, actinomycin D did not prevent DNA oligomerization, thus indicating that de novo viral protein synthesis is critical for viral apoptosis. In addition, the activation of caspase-3 was also detected in Vero cells by indirect fluorescent assay. From the present results, it is of future interest whether apoptotic characteristics of these viruses are related to pathogenecity in vivo.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Apoptosis/*physiology
		                        			;
		                        		
		                        			Bunyaviridae/*physiology
		                        			;
		                        		
		                        			Caspase 3
		                        			;
		                        		
		                        			Caspases/metabolism
		                        			;
		                        		
		                        			Cercopithecus aethiops
		                        			;
		                        		
		                        			Cytopathogenic Effect, Viral/*physiology
		                        			;
		                        		
		                        			DNA Fragmentation/physiology
		                        			;
		                        		
		                        			Dactinomycin
		                        			;
		                        		
		                        			Enzyme Activation
		                        			;
		                        		
		                        			Orbivirus/*physiology
		                        			;
		                        		
		                        			Vero Cells
		                        			
		                        		
		                        	
6.Immunogenicity of baculovirus expressed recombinant proteins of Japanese encephalitis virus in mice.
Dong Kun YANG ; Chang Hee KWEON ; Byoung Han KIM ; Seong In LIM ; Jun Hun KWON ; Seong Hee KIM ; Jae Young SONG ; Hong Ryul HAN
Journal of Veterinary Science 2005;6(2):125-133
		                        		
		                        			
		                        			Genes encoding for the premembrane and envelope (prME), envelope (E) and nonstructural protein (NS1) of Japanese encephalitis virus (JEV) were cloned. Each protein was expressed in baculovirus expression system. Of the three proteins expressed in baculovirus system, only prME had hemagglutination activity. The prME (72 and 54 kDa), E (54 kDa) and NS1 (46 kDa) proteins could be detected by Western blotting in the recombinant virus infected cells. Immunogenicity of the recombinant proteins obtained from infected Spodoptera frugiperda (Sf-9) cells was examined in mice. The 3 week-old ICR mice immunized intraperitoneally with three recombinant proteins three times were challenged with a lethal JEV. A survival rate was increased from about 7.7% in unimmunized mice to 92.3% in E + prME and only E groups. The complete protection was shown in prME and live vaccine inoculated groups, respectively. We also measured neutralizing antibody and three immunoglobulin subtypes of IgG1, IgG2a and IgG2b in the sera of mice before and after challenge. Titers of IgG1 antibodies were approximately two to three times higher than that of IgG2b antibodies in all the immunized groups as compared to the control group. However, IgG2a antibody level somewhat increased after challenge, indicating T-helper type 1 (Th1) cell response. The results of this study can provide useful information for developing efficacious subunit vaccine against JEV.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antibodies, Viral/blood
		                        			;
		                        		
		                        			Baculoviridae/genetics
		                        			;
		                        		
		                        			Blotting, Western
		                        			;
		                        		
		                        			Cloning, Molecular
		                        			;
		                        		
		                        			Encephalitis Virus, Japanese/genetics/*immunology
		                        			;
		                        		
		                        			Encephalitis, Japanese/*immunology/prevention&control
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Immunization
		                        			;
		                        		
		                        			Immunoglobulin Isotypes/blood
		                        			;
		                        		
		                        			Japanese Encephalitis Vaccines/*immunology/standards
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Mice, Inbred ICR
		                        			;
		                        		
		                        			Microscopy, Fluorescence
		                        			;
		                        		
		                        			Plasmids
		                        			;
		                        		
		                        			Recombinant Proteins/genetics/immunology
		                        			;
		                        		
		                        			Viral Envelope Proteins/genetics/*immunology
		                        			;
		                        		
		                        			Viral Matrix Proteins/genetics/*immunology
		                        			;
		                        		
		                        			Viral Nonstructural Proteins/genetics/*immunology
		                        			
		                        		
		                        	
7.Molecular characterization of full-length genome of Japanese encephalitis virus (KV1899) isolated from pigs in Korea.
Dong Kun YANG ; Byoung Han KIM ; Chang Hee KWEON ; Jun Hun KWON ; Seong In LIM ; Hong Ryul HAN
Journal of Veterinary Science 2004;5(3):197-205
		                        		
		                        			
		                        			We have determined the complete nucleotide and deduced amino acid sequences of the Japanese encephalitis virus (JEV) strain KV1899, isolated from a fattening pig in Korea. In comparison with 22 fully sequenced JEV genomes currently available, we found that the 10,963-nucleotide RNA genome of KV1899 has a 13-nucelotide deletion in the 3' non-translated variable region and 53 unique nucleotide sequences including 3' non-translated region (NTR). Its single open reading frame has a total of 28 amino acid substitutions. Comparison of the KV1899 genomic sequence with those of the 21 fully sequenced JEV strains in published databases showed nucleotide homology ranging from 97.4% (Ishikawa strain) to 87.0% (CH2195 strain). Amino acid homology with KV1899 strain ranged from 96.4% (K94P05) to 91.0% (GP78). The KV1899 showed the highest nucleotide homology with Ishikawa strain and the highest amino acid homology with K94P05. We performed an extensive E gene based phylogenetic analysis on a selection of 41 JEV isolates available from the GenBank. Compared with Anyang strain, isolated from a pig in 1969, that is current live vaccine strain for swine in Korea, the homology of nucleotide sequence in envelope gene was only 87.1%. The prM gene of the isolate was closely related with those of Ishikawa and K94P05 strains, which were grouped into genotype I of JEV.
		                        		
		                        		
		                        		
		                        			3' Untranslated Regions/chemistry/genetics
		                        			;
		                        		
		                        			Amino Acid Sequence
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Base Sequence
		                        			;
		                        		
		                        			Culicidae/virology
		                        			;
		                        		
		                        			Encephalitis Virus, Japanese/*genetics
		                        			;
		                        		
		                        			Encephalitis, Japanese/*veterinary/virology
		                        			;
		                        		
		                        			*Genome, Viral
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Membrane Glycoproteins/chemistry/genetics
		                        			;
		                        		
		                        			Molecular Sequence Data
		                        			;
		                        		
		                        			Phylogeny
		                        			;
		                        		
		                        			RNA, Viral/chemistry/genetics
		                        			;
		                        		
		                        			Reverse Transcriptase Polymerase Chain Reaction/veterinary
		                        			;
		                        		
		                        			Sequence Alignment
		                        			;
		                        		
		                        			Swine
		                        			;
		                        		
		                        			Swine Diseases/*virology
		                        			;
		                        		
		                        			Viral Envelope Proteins/chemistry/genetics
		                        			
		                        		
		                        	
8.TaqMan reverse transcription polymerase chain reaction for the detection of Japanese encephalitis virus.
Dong Kun YANG ; Chang Hee KWEON ; Byoung Han KIM ; Seong In LIM ; Seong Hee KIM ; Jun Hun KWON ; Hong Ryul HAN
Journal of Veterinary Science 2004;5(4):345-351
		                        		
		                        			
		                        			One step TaqMan reverse transcription polymerase chain reaction (RT-PCR) using TaqMan probe was developed for detection of Japanese encephalitis virus (JEV). Real-time RT-PCR was optimized to quantify JEV using the detection system (Rotor Gene 2000 detector) and dual-labeled fluorogenic probes. The gene specific labeled fluorogenic probe for the 3' non-translated region (3' NTR) was used to detect JEV. When the specificity of the assay using specific JEV primers was evaluated by testing three different JEV strains, other swine viruses and bovine viral diarrhea virus, no cross-reactions were detected with non-JE reference viruses. A single tube TaqMan assay was shown to be 10-fold more sensitive than the conventional two-step RT-PCR method. Detection limits of two step and real-time RT-PCR for JEV were 112 TCID50 /ml and 11.2 TCID50 /ml, respectively. Quantification of JEV was accomplished by a standard curve plotting cycle threshold values (Ct ) versus infectivity titer. Real-time RT-PCR assay using single tube method could be used as a sensitive diagnostic test, and supplied the results in real time for detection and quantification of JEV. We could detect JEV RNA genome in plasma samples of pigs inoculated with KV1899 strain at 2 days post inoculation, but couldn't in 41 fetus samples. This assay was sensitive, specific, rapid and quantitative for the detection of JEV from laboratory and field samples.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			DNA Primers/chemistry
		                        			;
		                        		
		                        			DNA Probes/chemistry
		                        			;
		                        		
		                        			Encephalitis Virus, Japanese/genetics/*isolation&purification
		                        			;
		                        		
		                        			Encephalitis, Japanese/diagnosis/*veterinary/virology
		                        			;
		                        		
		                        			RNA, Viral/analysis
		                        			;
		                        		
		                        			Reproducibility of Results
		                        			;
		                        		
		                        			Reverse Transcriptase Polymerase Chain Reaction/methods/*veterinary
		                        			;
		                        		
		                        			Sensitivity and Specificity
		                        			;
		                        		
		                        			Swine
		                        			;
		                        		
		                        			Swine Diseases/*diagnosis/virology
		                        			;
		                        		
		                        			*Taq Polymerase
		                        			
		                        		
		                        	
9.Biophysical characterization of Japanese encephalitis virus (KV1899) isolated from pigs in Korea.
Dong Kun YANG ; Byoung Han KIM ; Chang Hee KWEON ; Jun Hun KWON ; Seong In LIM ; Hong Ryul HAN
Journal of Veterinary Science 2004;5(2):125-130
		                        		
		                        			
		                        			A virus strain, showing cytopathic effect in Vero cell, was isolated from plasma of a fattening pig in Gyeonggi province, Korea in October 1999. The evaluation of physicochemical/biological properties of the isolate showed that the virus, KV1899, inoculated suckling mouse showed paralysis and died within 7 days post-inoculation, the mouse brain suspension had hemagglutinating activity with goose RBC. Pathogenicity of isolate was carried out by intracranial and intraperitoneal inoculation of 3-4 weeks mice. The mice inoculated with isolate showed 10 4.5 LD50/ 0.03 ml and 10 3.0 LD50/0.5 ml according to the inoculation route. The isolate was identified as RNA and enveloped virus using IUDR and chloroform sensitivity test. The virus particles within the infected Vero cell were measured to be 40-50 nm in size by electron microscopy. The isolate was further characterized by immuno-fluorescence assay using Japanese encephalitis virus (JEV) specific monoclonal antibodies. Reverse transcription polymerase chain reaction (RT-PCR) revealed the presence of JE specific conserved sequences in this isolate. The artificially inoculated pigs had HI titer of 320 to 2,560 against JEV at 14 to 42 days post inoculation. We confirmed this isolate as Japanese encephalitis virus. It was the second isolation of JEV in pigs in Korea.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antibodies, Viral/analysis
		                        			;
		                        		
		                        			Cercopithecus aethiops
		                        			;
		                        		
		                        			Cytopathogenic Effect, Viral
		                        			;
		                        		
		                        			Encephalitis Virus, Japanese/*classification/*isolation & purification/ultrastructure
		                        			;
		                        		
		                        			Encephalitis, Japanese/pathology/*veterinary/virology
		                        			;
		                        		
		                        			Fluorescent Antibody Technique, Indirect/veterinary
		                        			;
		                        		
		                        			Hemagglutination Inhibition Tests/veterinary
		                        			;
		                        		
		                        			Hemagglutination Tests/veterinary
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Microscopy, Electron/veterinary
		                        			;
		                        		
		                        			RNA, Viral/analysis
		                        			;
		                        		
		                        			Reverse Transcriptase Polymerase Chain Reaction/veterinary
		                        			;
		                        		
		                        			Swine
		                        			;
		                        		
		                        			Swine Diseases/pathology/*virology
		                        			;
		                        		
		                        			Vero Cells/virology
		                        			
		                        		
		                        	
10.An Acoustic and Radiologic Study on Voice Change after Laser Assisted Uvulopalatoplasty.
Chang Hun LEE ; Hwan Jung ROH ; Jun Ho YUN ; Chi Hoon CHOI ; Soo Kweon KOO ; Sang Hwa LEE
Korean Journal of Otolaryngology - Head and Neck Surgery 2002;45(8):811-816
		                        		
		                        			
		                        			BACKGROUND AND OBJECTIVES: Many people have been concerned about voice change after laser assisted uvulopalatoplasty (LAUP). A number of studies reported acoustic changes after uvulopalatopharyngoplasty (UPPP) and LAUP. However, there have not been any reports on the association between anatomic change and acoustic results after LAUP. The purpose of this study is to analyze changes in the voice and changes in the vocal tract after LAUP and to evaluate whether the anatomical changes of vocal tract have an effect on the voice change or not. SUBJECTS AND METHOD: By using CSL, we analyzed fourteen LAUP cases on the formant frequencies of six vowels (/a/, /i/, /u/, /=, /o/, /e/) and four nasal consonants (/hana/, /eomma/, /eoungga/, /chiken/). By using MR image, we analyzed changes in the vocal tract eight weeks after LAUP with preoperative findings in three cases. RESULTS: In acoustic analysis, the second formant frequencies of /u/ and /= phonation were significantly reduced postoperatively compared to those of preoperative status. In imaging study of /u/ and /=, the uvula and soft palate were contracted, so coupling was occurred between nasal cavity and oropharynx in /u/ and /= phonation and the tongue was shifted toward posterior pharyngeal wall to compensate coupling. CONCLUSION: LAUP reduced the second formant of /u/ and /=, which did not result in serious voice changes.
		                        		
		                        		
		                        		
		                        			Acoustics*
		                        			;
		                        		
		                        			Nasal Cavity
		                        			;
		                        		
		                        			Oropharynx
		                        			;
		                        		
		                        			Palate, Soft
		                        			;
		                        		
		                        			Phonation
		                        			;
		                        		
		                        			Tongue
		                        			;
		                        		
		                        			Uvula
		                        			;
		                        		
		                        			Voice*
		                        			
		                        		
		                        	
            
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