Division of Social Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Chemosphere. 2013 Aug;92(7):772-7. doi: 10.1016/j.chemosphere.2013.04.005. Epub 2013 May 4.
In 1968, many people developed dioxin poisoning (Yusho) in Japan. Ingestion of 2,3,4,7,8-pentachlorodibenzofuran (2,3,4,7,8-PeCDF) was considered to be the cause of this poisoning. Although some patients had high concentrations of 2,3,4,7,8-PeCDF in their blood, individuals' half-lives of 2,3,4,7,8-PeCDF were long.
To evaluate the relationship between clinical and laboratory parameters and the individual half-life of 2,3,4,7,8-PeCDF in blood.
Clinical and laboratory data were collected during annual check-ups from 2001 to 2008. We enrolled 71 patients, who were measured more than 3 times, and who had 2,3,4,7,8-PeCDF concentrations in blood >50pgg(-1) lipid. The half-life of 2,3,4,7,8-PeCDF for each patient was estimated using linear regression. Moreover, relationships between clinical and laboratory parameters and individual half-life were investigated by linear regression.
A shortened individual half-life for 2,3,4,7,8-PeCDF was significantly correlated with an increased red blood cell count, increased viscous secretions from the meibomian glands, existing black comedones, and severe cedar pollen allergy.
Symptoms that accelerate excretion of lipids from the body, such as viscous secretions from the meibomian glands, may lead to a shorter half-life of 2,3,4,7,8-PeCDF. Red blood cells are related to the half-life of 2,3,4,7,8-PeCDF. However, further studies are required to investigate the excretory mechanism of 2,3,4,7,8-PeCDF.
1968 年,许多日本人发生了二噁英中毒(油症)。摄入 2,3,4,7,8-五氯二苯并呋喃(2,3,4,7,8-PeCDF)被认为是导致这种中毒的原因。尽管一些患者血液中的 2,3,4,7,8-PeCDF 浓度很高,但个体的 2,3,4,7,8-PeCDF 半衰期较长。
评估临床和实验室参数与血液中 2,3,4,7,8-PeCDF 个体半衰期之间的关系。
在 2001 年至 2008 年的年度检查中收集了临床和实验室数据。我们招募了 71 名患者,这些患者的测量次数超过 3 次,并且血液中的 2,3,4,7,8-PeCDF 浓度>50pg/g 脂质。使用线性回归估计每位患者的 2,3,4,7,8-PeCDF 半衰期。此外,通过线性回归研究了临床和实验室参数与个体半衰期之间的关系。
2,3,4,7,8-PeCDF 的个体半衰期缩短与红细胞计数增加、睑板腺粘性分泌物增加、存在黑头粉刺和严重雪松花粉过敏显著相关。
从身体中加速脂质排泄的症状,如睑板腺粘性分泌物,可能导致 2,3,4,7,8-PeCDF 的半衰期缩短。红细胞与 2,3,4,7,8-PeCDF 的半衰期有关。然而,需要进一步研究来探讨 2,3,4,7,8-PeCDF 的排泄机制。