中华流行病学杂志
中華流行病學雜誌
중화류행병학잡지
CHINESE JOURNAL OF EPIDEMIOLOGY
2011年
6期
559-564
,共6页
翁小满%李康%温艳%邢燕%刘健%洪炳和%李桓英%Varalakshmi Vissa
翁小滿%李康%溫豔%邢燕%劉健%洪炳和%李桓英%Varalakshmi Vissa
옹소만%리강%온염%형연%류건%홍병화%리환영%Varalakshmi Vissa
麻风%传播%病例发现
痳風%傳播%病例髮現
마풍%전파%병례발현
Leprosy%Transmission%Case-finding
目的 探讨云南省丘北县多种药物联合化疗实施25年后麻风仍持续传播的影响因素.方法 分别采用ELISA、PCR检测高流行区患者与家庭内接触者、普通人群血清中麻风菌特异性PGL-1抗体以及鼻分泌物中的麻风菌,采用PCR方法检测疫村环境水中的麻风菌.采用数目可变的串联重复序列基因分型方法探讨麻风菌传播途径及传播链等.结果 在2001年以前从麻风患者家庭成员中检测到的比例低,而延迟期>2年患者的检出比例高.2001年后防治工作加强使这两个指标改进,但麻风发现率仍一直维持在4/10万至5/10万.疫村人群PGL-1抗体阳性率为20%~30%,主要感染人群为青少年;不仅从患者、家内接触者的鼻分泌物与环境水中检出麻风菌,且与未经治疗患者的皮肤组织和鼻分泌物中麻风菌基因型一致.菌株分型证实该县北部地区不仅有多个高发家庭聚集,而且家庭内患者的菌株基因型一致.在北部地区基因型匹配菌株的比例高于南部地区.结论 丘北县麻风在家庭内和疫村中的传播严重,疫村环境水中存在麻风菌等是影响该病持续传播的重要因素.
目的 探討雲南省丘北縣多種藥物聯閤化療實施25年後痳風仍持續傳播的影響因素.方法 分彆採用ELISA、PCR檢測高流行區患者與傢庭內接觸者、普通人群血清中痳風菌特異性PGL-1抗體以及鼻分泌物中的痳風菌,採用PCR方法檢測疫村環境水中的痳風菌.採用數目可變的串聯重複序列基因分型方法探討痳風菌傳播途徑及傳播鏈等.結果 在2001年以前從痳風患者傢庭成員中檢測到的比例低,而延遲期>2年患者的檢齣比例高.2001年後防治工作加彊使這兩箇指標改進,但痳風髮現率仍一直維持在4/10萬至5/10萬.疫村人群PGL-1抗體暘性率為20%~30%,主要感染人群為青少年;不僅從患者、傢內接觸者的鼻分泌物與環境水中檢齣痳風菌,且與未經治療患者的皮膚組織和鼻分泌物中痳風菌基因型一緻.菌株分型證實該縣北部地區不僅有多箇高髮傢庭聚集,而且傢庭內患者的菌株基因型一緻.在北部地區基因型匹配菌株的比例高于南部地區.結論 丘北縣痳風在傢庭內和疫村中的傳播嚴重,疫村環境水中存在痳風菌等是影響該病持續傳播的重要因素.
목적 탐토운남성구북현다충약물연합화료실시25년후마풍잉지속전파적영향인소.방법 분별채용ELISA、PCR검측고류행구환자여가정내접촉자、보통인군혈청중마풍균특이성PGL-1항체이급비분비물중적마풍균,채용PCR방법검측역촌배경수중적마풍균.채용수목가변적천련중복서렬기인분형방법탐토마풍균전파도경급전파련등.결과 재2001년이전종마풍환자가정성원중검측도적비례저,이연지기>2년환자적검출비례고.2001년후방치공작가강사저량개지표개진,단마풍발현솔잉일직유지재4/10만지5/10만.역촌인군PGL-1항체양성솔위20%~30%,주요감염인군위청소년;불부종환자、가내접촉자적비분비물여배경수중검출마풍균,차여미경치료환자적피부조직화비분비물중마풍균기인형일치.균주분형증실해현북부지구불부유다개고발가정취집,이차가정내환자적균주기인형일치.재북부지구기인형필배균주적비례고우남부지구.결론 구북현마풍재가정내화역촌중적전파엄중,역촌배경수중존재마풍균등시영향해병지속전파적중요인소.
Objective To explore the factors influencing the steady transmission of leprosy as indicated by new case detection rate in Qiubei county, Yunnan province, China despite the implementation of MDT for the last 25 years. Methods Information related to case-finding was collected. ELISA and PCR were applied to detect anti-PGL-1 antibody in sera and Mycobacterium leprae in nasal secretions respectively, in leprosy patients, their household contacts and the general population. M. leprae by PCR was also detected from water in the highly endemic villages. VNTR typing was performed to explore the mode and chain of transmission of M. leprae. Results Prior to 2001, the proportion of new cases detected from the examination of household contacts of leprosy patients was low (number, compared to), while the proportion of patients whose identification was delayed by more than 2 years, was high (number, compared to). Qualities of these two indicators has been improved, along with the improvement of leprosy control program since 2001, but the detection rates has been steady at 4-5/ 100 000 during 1986-2010. The PGL-1 seropositivity rate was 20%-30% in general population, with the peak rate (30%) detected in the teenage population in the endemic villages. In addition to the fact that M. leprae was detected in nasal secretion from patients, their contacts and from water, the M. leprae VNTR genotypes were found to be highly similar between skin biopsy and nasal secretion in untreated cases. Families with multi-cases were clustered and located in the Northern part of the County, and the genotypes of M. leprae were identical within those families. The percentage of clusters was considerably higher in Northern rather than Southern parts of the County. Conclusion Results from this molecular study demonstrated evidence that transmission of leprosy within the families and in the endemic-villages was severe. M. leprae were detected in waters from the endemic villages and others areas which might have a relation to the continued transmission of leprosy.