• Journal of Oral Medicine and Pain
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• 제32권4호
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• pp.347-355
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• 2007

본 연구는, 양극 벗김 전압전류법 (Anodic stripping voltammetry: ASV)을 이용하여, 전처리 과정 (pre-treatment procedure)에 따른 인체 타액내 납 (Pb)과 카드뮴 (Cd)의 검출농도의 차이를 비교하기 위하여 시행되었다. 납과 카드뮴에 노출되지 않을 것으로 추정되는 남녀 10명을 대상으로, 비자극성 전타액을 채취한 후, 각 시료를 6개의 시편으로 나누어서 원심분리를 시행한 후 3가지 전처리를 하는 경우와 원심분리를 시행하지 않고 3가지 전처리를 하는 경우로 구분하였다. 타액의 전처리법은 simple dilution by electrolyte, simple dilution by HCl, acid digestion by nitric acid 등 3가지를 각각 시행했으며, ASV법으로 타액 내 납과 카드뮴의 농도를 분석하였다. 실험결과는 다음과 같다. 1. '타액 시료의 전처리 방법에 따른 타액내 납의 평균 농도'를 살펴보면, 원심분리 시행군이 원심분리 미시행군에 비하여 평균농도가 유의성 있게 높았다. 2. 타액내 납의 검출에 있어서, 단순히 전해질로 희석만 한 경우보다 염산이나 질산으로 전처리를 시행한 경우에 유의성 있게 더 높은 농도를 나타내었다. 3. '타액 시료의 전처리 방법에 따른 타액내 카드뮴의 평균 농도'를 살펴보면, 원심분리 시행군이 원심분리 미시행군에 비하여 평균농도가 유의성 있게 높았다. 4. 타액내 카드뮴의 검출에 있어서, 단순히 전해질로 희석만 한 경우보다 염산이나 질산으로 전처리를 시행한 경우가 더 높은 농도를 나타내었으나, 유의한 차이는 아니었다.

• Journal of Oral Medicine and Pain
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• 제26권4호
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• pp.331-343
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• 2001

Advances in medical procedures and utilization of medication have resulted in expanding aged population, which leads to increased aged patients with salivary hypofunction and its associated symptoms in dental clinic. The purpose of this study was to investigate clinical characteristics of patients with dry mouth and its correlation with their salivary flow rate. Forty dry mouth patients (7 males, 33 females, mean age 42.0 years) whose flow rate of unstimulated whole saliva was less than 0.15 ml/min were included and their gender- and age-matched controls (7 males, 33 females, mean age 42.9 years) who did not report any complaints, suggestive of salivary gland dysfunction and had the flow rate of greater than 0.20 ml/min were included for comparison. The salivary flow rate was measured in both unstimulated and stimulated conditions. Dry mouth-related clinical information including history, dry mouth associated symptoms, exacerbating and relieving factors, drugs, systemic diseases, and family history was investigated using questionnaires. The differences in distribution of patients and control subjects to each question and their relation to the salivary flow rate were analyzed and we came to following conclusions. 1. There were statistically significant differences in the distribution of patients and controls to the following questions: the period and frequency of suffering from dry mouth; severity of dry feeling during a meal; severity of discomfort during swallowing; necessity of sipping liquids during swallowing dry foods, severity of discomfort in usual life due to dry feeling; self-assessment of residual salivary volume; taking medications. 2. The patients had more stress-related medical histories including indigestion, insomnia, and gastritis compared with controls. The patients took many kinds of medications to control their systemic diseases. 3. There were statistically significant differences in the salivary flow rate between different groups of patients to following questions: severity of dry feeling during a meal; severity of discomfort during swallowing; necessity of sipping liquids during swallowing dry foods. The difference was more significant in the case of stimulated salivary flow rate rather than unstimulated one. 4. The salivary flow rate of patients taking medications was significantly less than that of patients who did not take medications. The difference was more significant in the case of stimulated salivary flow rate rather than unstimulated one.

• 대한소아치과학회지
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• 제26권2호
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• pp.262-274
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• 1999

구강내의 불소농도를 증가시키는 여러 방법에는 불화된 상수도를 섭취하거나 불소보조제를 복용하는 전신적 투여방법과 불소치약, 불소양치액, 불소젤의 도포와 같은 국소적 투여방법이 있다. 그동안 다양한 delivery system을 통한 국소도포용 불소제제가 임상적으로 우식증을 예방하는데 도움이 된다는 사실이 확인되었다. 최근의 연구에서 불소의 항우식효과는 치아주위의 oral fluid environment속에서 불소의 중요성을 지적하고 있다. 비자극성 전타액내 불소농도는 주어진 시간동안 치면과 상호작용이 가능한 aqueous phase의 불소를 나타낸다고 한다. 따라서 타액내의 불소 농도를 조사함으로써 간접적으로 우식예방효과에 대한 정보를 얻을 수 있다. 우식증예방을 위해 환자에게 여러 가지 국소도포방법 중 한 가지를 추천하기에 앞서 이들 각 방법이 타액내 불소농도를 증가시키는데 얼마나 효과적인지 알 필요가 있다. 이에 저자는 국소적 불소도포후 구강내 불소의 잔류량과 시간별 농도를 비교하고자 현재 국내에서 많이 쓰이고 있는 서로다른 네가지 불소제제를 사용하고 난 뒤 시간변화에 따른 타액내 불소농도를 HMDS를 이용한 확산법과 불소이온전극을 사용하여 측정하고 다음과 같은 결과를 얻었다. 1. 비자극성 혼합타액내 평균 불소농도는 $0.0152ppm{\pm}0.0091ppm$이었으며, 비자극성 타액분비율은 0.34-0.36ml/min으로 각군간에 통계적 유의차는 없었다. 2. 불소제제 사용직후를 제외하고는 모든 구간에서 타액내 불소 농도는 APF gel군>neutral gel군>불소양치액군>불소치약군의 순이었고, 불소처치 120분 경과후 불소치약군의 타액내 불소농도가, 180분 경과후 불소양치액군의 불소농도가 대조군과 통계적 유의차를 보이지 않은 반면, 6시간 경과후까지 APF gel군과 neutral gel군의 타액내 불소농도가 대조군에 비해 유의성있게 높게 유지되었다(p<0.05). 3. 불소제제 사용직후부터 120분 경과후까지 타액내 잔류불소량($AUC_{0-120min}$)은 neutral gel군>APF gel군>불소양치액군>불소치약군의 순이었고, neutral gel군과 APF gel군이 대조군과 나머지 두 군에 비해 유의하게 높은 값을 보였다(p<0.05).

• Journal of Oral Medicine and Pain
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• 제23권2호
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• pp.109-117
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• 1998

Fixed orthodontic appliances for the treatment of malocclusion has iatrogenic side effect such as demineralization of enamel, gingivitix and gingival hyperplasia. The purpose of this study is to longitudinally investigate the salivary microorganisms and immunoglobulin A after delivery of fixed orthodontic appliances for 10 months. Eight orthodontic patients were included in this study and the author has investigated the numbers of general bacteria, Streptococcus mutans Staphylococcus aureus and concentration of immunoglobulin A from unstimulated whole saliva. The author examined these parameters at prebracketing, 1 month after, 4 months after, 7 months after and 10 months after delivery of fixed orthodontic appliances. The obtained results were as follows : There were significant increases in the number of salivary general bacteria, Streptococcus mutans and Staphylococcus aureus after delivery of fixed orthodontic appliances The numbers of general bacteria were significantly increased at 1 month after (p<005), 4 months after (p<0.05), 7 months after (p<0.01), compared with prebracketing. However it showed no difference at 10 month after compared with 7 months after bracketing. The Numbers of Staphylococcus aureus were significantly increased at 1 month after (p<0.05), 4 months after(p<0.01), 7 month(p<0.01), compared with prebracketing. However it showed decreasing pattern at 10 months after compared with 7 months after bracketing. There was no significant difference in the concentration of immunoglobulin A after delivery of fixed orthodontic appliances.

• Journal of Oral Medicine and Pain
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• 제42권3호
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• pp.72-80
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• 2017

Purpose: Pilocarpine as a salivation stimulant in pill form has mostly been used to relieve oral dryness for xerostomic patients but its use may often be limited due to variable side effects from systemic absorption. Therefore, the purpose of this study was to investigate the effects of pilocarpine mouthwash on salivation according to the variable concentration and duration for healthy volunteers. Related adverse effects and subjective assessment on its effects on salivation were also examined. Methods: This study was performed as placebo-controlled, double-blind, randomized clinical trial. Thirty healthy volunteers (male=23, mean age=22.2 years) were randomly allocated to 6 groups with the different concentration of pilocarpine mouthwash (placebo, 0.1%, 0.5%, 1.0%, 1.5%, and 2.0%). The whole experiment consisted of 3 sessions according to the duration of mouthwash, i.e., 1, 3, and 5 minutes with the mean wash-out period ${\geq}2$ days between the sessions. Unstimulated whole saliva was collected before and after gargling with a mouthwash. Results: Salivation of the higher concentration groups ${\geq}1%$ significantly increased than those of lower concentration group. The application period of mouthwash did not cause any changes of salivary flow rate at the higher concentrations ${\geq}1.0%$. The lower concentrations of 0.5% and 0.1% had no effects on salivation even after 5-minute mouthwash. There was no significant difference between blood pressure and pulse rate before and after use of mouthwash. Conclusions: From the results of the current study, pilocarpine mouthwash with at least 1.0% concentration more than a minute might be clinically effective in salivation without any serious side effects. Dose of mouthwash rather than duration seems to be a critical factor to salivation.

• Journal of Oral Medicine and Pain
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• 제40권1호
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• pp.10-16
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• 2015

Purpose: Pilocarpine has the effects on improvement of salivary flow and subjective symptoms for xerostomic patients. Because of unwanted side effects following its systemic administration, topical pilocarpine has been paid attention as an alternative. This study aimed to investigate effects of pilocarpine solution as mouthwash on salivary flow and adverse effects compared to systemic administration of 5 mg pilocarpine tablet in healthy subjects. Methods: The study was a double blind, placebo-controlled, crossover clinical trial. Five milligrams pilocarpine tablets, 4 mL of 2% pilocarpine solution and placebo solution were given to 12 healthy volunteers (6 males and 6 females) in a predetermined order with wash-out period of at least two days and unstimulated whole saliva was collected before and after administration of each drug. Blood pressure and pulse rate was also measured and subjective effect and potential side effects were evaluated by a self-administrated questionnaire. Results: Systemic (5 mg tablet) and topical (2% solution) use of pilocarpine significantly increased salivary flow rate in healthy subjects compared to placebo (p<0.001). In both the pilocarpine solution and tablet groups, salivary flow rates at 120 minutes after administration remained increased. Subjective effect on salivation was the largest in the pilocarpine tablet group, followed by the pilocarpine solution group (p<0.05). There was no significant difference in blood pressure and pulse rate after administration of all three drugs. Fewer side effects reported in the pilocarpine solution group than in the tablet group. Conclusions: Two percents pilocarpine solution as mouthwash increases salivary flow rate, definitely superior to placebo solution and comparable to pilocarpine tablet, with fewer side effects in healthy subjects. It indicates a possibility of pilocarpine solution as a useful alternative of pilocarpine tablets for the xerostomic patients with systemic diseases.

• Journal of Oral Medicine and Pain
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• 제44권1호
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• pp.25-30
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• 2019

Purpose: The exact causes of burning mouth syndrome (BMS) is unclear so far. There are many studies to elucidate the relation between oral disease and genetic predisposition. In this study, we first tried to investigate salivary exosomal genetic components that could play an important role for diagnosing and elucidating the progression of BMS. Methods: We compared salivary exosomal micro RNAs (miRNAs) of BMS Patients to those of control using next generation sequencing (NGS). Unstimulated whole saliva from 15 patients with BMS and 10 control subjects were divided into two sets. Isolated exosomes and their total RNAs were subject to NGS for the screening of miRNAs. Results: There were up-regulated 10 exosomal miRNAs (hsa-miR-1273h-5p, hsa-miR-1273a, hsa-miR-1304-3p, hsa-miR-4449, hsa-miR-1285-3p, hsa-miR-6802-5p, hsa-miR-1268a, hsa-miR-1273d, hsa-miR-1273f, and hsa-miR-423-5p) and down-regulated 18 exosomal miRNAs (hsa-miR-27b-3p, hsa-miR-16-5p, hsa-miR-186-5p, hsa-miR-142-3p, hsa-miR-141-3p, hsa-miR-150-5p, hsa-miR-374a-5p, hsa-miR-93-5p, hsa-miR-29c-3p, hsa-miR-29a-3p, hsa-miR-148a-3p, hsa-miR-22-3p, hsa-miR-27a-3p, hsa-miR-424-5p, hsa-miR-19b-3p, hsa-miR-99a-5p, hsa-miR-548d-3p, and hsa-miR-19a-3p) in BMS patients comparing with those of control subjects. Conclusions: We show that there are 28 differential expression of miRNAs between the patients with BMS and those of control subjects. The specific function of indicated miRNAs should be further elucidated.

• Asian Pacific Journal of Cancer Prevention
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• 제16권14호
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• pp.5773-5777
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• 2015

Background: Oral squamous cell carcinoma (OSCC) is thought to develop from precancerous dysplastic lesions through multistep processes of carcinogenesis involving activation of oncogenes and loss of tumor suppressor genes. The human epidermal growth factor receptor 2 (Her-2/neu [erbB-2]), a cell membrane glycoprotein, is a growth factor receptor that has receptor tyrosine kinase activity. Her2/neu activation plays a central role in cell proliferation and survival. It has been shown that overexpression of Her2/neu increases the rate of cell division and growth, leading to precancerous changes. The aim of the present study was to compare the serum and salivary Her2/neu levels between cases with premalignant and malignant oral lesions. Materials and Methods: Fasting blood samples and unstimulated saliva by passive drooling were collected from three groups of healthy control (n=20), premalignant disorder (PMD) (n=20) and OSCC (n=25) subjects. The HER2 extracellular domain (HER2 ECD) levels were measured using ELISA. Results: The levels of serum Her2/neu showed no significant differences between any of the groups but on the other hand salivary Her2/neu levels were found to be significantly (p<0.05) higher when compared between control (median 68.7 pg/ml, range: 21.5 - 75.8) and OSCC (median 145.6 pg/ml, range: 45.1-191.1). A similar trend was observed when comparing between PMD (median 43.3, range: 22.1 -94.7) and OSCC with a statistical significance of p<0.05. Conclusions: Our study provided evidence of increased salivary Her2/neu in OSCC when compared to PMD and control which was not the case for serum levels. This suggests that probably Her2/neu is not highly amplified as in breast cancer so as to be reflected in serum. Since saliva is in local vicinity of the OSCC, even a mild increase might be mirrored. On the whole, this study proposes Her2/neu as marker for distinguishing premalignant and malignant conditions.

• 대한소아치과학회지
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• 제40권2호
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• pp.89-97
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• 2013

연구의 목적은 인체 안정성이 입증된 고분자제제인 폴리비닐알코올(PVA, polyvinyl alcohol)로 얇은 박막을 제조하고 불화나트륨(NaF)을 첨가하여 불소를 함유한 고분자 접착 테이프(NaF-PVA)를 개발하여 피실험자의 구강 내에 도포 후 잔류하는 불소농도를 측정하였다. 이를 통해 제제 도포 전후의 타액 내 불소농도를 분석하여 불소를 함유한 고분자 접착 테이프의 치아우식증 예방효과를 간접적으로 평가하였다. 불소겔(60seconds taste$^{(R)}$, Group 1), 불소바니쉬(FluoroDose$^{(R)}$ varnish, Group 2)와 불소를 함유한 고분자 접착 테이프(NaF-PVA, Tiral product, Group 3)를 각각 15명씩 상악 치아 12개의 순면에 도포 후, 1시간, 3시간, 6시간, 12시간, 24시간, 48시간 후 비자극성 타액 내 불소농도를 불소이온전극을 이용하여 측정하였다. 도포 후 3시간까지 세 군 모두 불소제제 도포 전 농도보다 유의하게 높은 불소농도를 보였으며 3군의 경우 도포 후 6시간에서도 불소제제 도포 전 농도보다 유의하게 높은 불소농도를 보였다(p < 0.05). 도포 후 6시간에서 3군은 1군과 2군보다 유의하게 높은 불소농도를 보였고 (p < 0.05), 1군과 2군 사이의 유의한 차이는 없었다(p > 0.05).

• Journal of Oral Medicine and Pain
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• 제34권4호
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• pp.341-351
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• 2009

사람들은 미각을 통해 음식물의 영양분과 안전성 여부를 파악하고, 이를 통해 식욕이 자극되고 만족되므로 미각은 음식물을 섭취하는데 필수적인 역할을 한다고 할 수 있다. 미각이 상실되거나 왜곡된 환자들의 경우 섭식 양상에 변화를 일으켜 건강에 나쁜 영향을 미치게 될 수 있다. 미각 기능에 영향을 줄 수 있는 요소는 매우 다양하며 미각의 장애 양상 또한 매우 다양하게 나타날 수 있다. 하지만 미각은 주관적인 감각으로 다른 감각들과는 달리 객관적으로 평가하기가 까다로우며, 맛을 느끼는데 있어서 미각뿐 아니라 후각, 촉각, 온도감각, 심리 상태 등 여러 다른 요소들의 영향을 받으므로 미각 이상을 나타내는 환자들을 진단하고 치료하는 것은 매우 어려운 일이다. 그러므로 실제 임상적 상황에서 미각장애의 평가를 위해서는 무엇 보다도 신중하고 철저한 병력청취와 임상적 증상의 분석을 통하여 환자의 상태를 정확히 평가하는 것이 가장 중요하다. 미각은 시각이나 청각과 같은 다른 감각에 비해 그 동안 주목을 받아오지 못한 분야였으나, 사회가 발달함에 따라 삶의 질을 중시하게 됨으로써 최근 미각 장애로 내원하는 환자가 증가하는 추세이다. 본 연구의 목적은 미각 장애를 주소로 내원한 환자들의 임상적 특성을 분석하는 것이다. 미각 장애를 주소로 2005년 11월부터 2008년 8월까지 서울대학교 치과병원 구강내과에 내원한 환자 50명(남 12명, 여 38명, 평균 연령 $53.6\;{\pm}\;14.7$ 세)을 대상으로 하였다. 상담을 통하여 현재 미각 장애의 증상과 관련된 사항들과 그 밖의 의과적 치과적 병력, 투약, 미각 장애 외의 구강 증상들에 대하여 조사하였으며, 구강 검진, 설문지 작성, 방사선 사진 촬영, 혈액검사, 타액분비율 측정 검사 등의 임상적 검사를 시행하여 다음과 같은 결과를 얻었다. 1. 미각 장애 환자들 중 구강 점막의 통증 혹은 작열감을 호소한 환자가 36명(72%)이었다. 이들 중 구강점막에 특별한 병소를 보이지 않는 구강작열감증후군으로 진단된 환자는 18명(36%)이었다. 2. 전체 환자들 중 19명(38%)의 환자가 주관적 구강건조감을 호소하였으며, 타액분비율 측정 결과 비자극시 타액분비율이 0.1 mL/min 이하인 환자는 14명(28%)이었고, 자극시 타액분비율이 0.5 mL/min 이하인 환자는 17명(34%)이었다. 3. 미각 장애의 종류로는 미각감소(hypogeusia)가 25명(50%)으로 가장 많았으며, 미각왜곡(dysgeusia)이 18명(36%), 환상미 각 (phantogeusia)이 15명(30%), 미각과민(hypergeusia)이 10명(20%), 미각상실(ageusia)이 5명(10%) 이었다. 전체 50명 중 19명(38%)의 환자가 두 가지 이상의 미각 장애의 종류를 나타내었으며, 가장 많은 조합은 미각왜곡과 미각감소를 같이 보이는 경우였다. 4. 미각 장애의 원인이나 관련요인은 병력조사와 임상검사를 토대로 평가하였으며, 구강점막질환이나 원인불명인 경우가 각각 9명(18%)으로 가장 많았다. 그 밖에 심인성이 8명(16%), 약물이 7명(14%), 구강건조증이 6명(12%)으로 나타났으며, 이 5가지의 항목이 전체의 78%를 차지하였다.