{"title":"两项研究的故事:外周嗜酸性粒细胞增多与在成人粪便样本中检测到脆弱片阿米巴是否有关?","authors":"Priya Garg , John Chetwood , Thuy Phan , Timothy Gray , Genevieve McKew","doi":"10.1016/j.pathol.2024.01.011","DOIUrl":null,"url":null,"abstract":"<div><p>The protozoan parasite <em>Dientamoeba fragilis</em> is a frequently isolated stool organism and postulated cause of gastrointestinal symptoms. Peripheral blood eosinophilia has been described. This is the first study amongst the Australasian adult population to assess the relationship between organism detection and eosinophilia.</p><p>A case-control study took place over 7 years at a single Sydney laboratory site, evaluating patients with <em>D. fragilis</em> identified on stool using real-time PCR with a recent full blood count, to control groups with <em>Giardia</em> spp. and sequential negatives with neither organism. A nested study compared those with microscopic evidence of <em>D. fragilis</em> as a marker of disease burden, to molecular diagnosis alone.</p><p>Sixty-four <em>D. fragilis</em>, 30 <em>Giardia</em> spp., and 94 sequential controls were enrolled. Only 60.1% of samples were preserved in sodium acetate-acetic acid formalin (SAF) fixative, indication mostly not documented. The major co-organism detected amongst all participants was <em>Blastocystis</em> sp., particularly in the <em>D. fragilis</em> cohort (37.2%). The most common pathogen amongst sequential controls was <em>Campylobacter</em> spp. (7.4%). Patients with <em>D. fragilis</em> were more likely (12.5%) to have a clinically significant eosinophilia (>0.5×10<sup>9</sup>/L) compared to those with <em>Giardia</em> spp. (3.3%) or sequential controls (4.3%) (<em>p</em>=0.03). A significant difference was also noted in the overall median eosinophil count of those with <em>D. fragilis</em> versus all controls (0.2 vs 0.1×10<sup>9</sup>/L, <em>p</em>=0.01); however, this was within the reference interval (where up to >0.5×10<sup>9</sup>/L is accepted in healthy individuals within a typical population). No eosinophil difference was found between those with molecular versus additional microscopic detection of <em>D. fragilis</em> (0.1 vs 0.1×10<sup>9</sup>/L).</p><p>These results support an association between the identification of clinically significant peripheral blood eosinophilia and <em>D. fragilis</em> presence, which may impact the diagnostic approach to the patient with unexplained eosinophilia. Further prospective trials may help assess any significance further and the implication of co-carriage with other enteric organisms. The importance of clinical indication and need for appropriate fixative media in diagnostic parasitology are also highlighted.</p></div>","PeriodicalId":19915,"journal":{"name":"Pathology","volume":"56 5","pages":"Pages 688-695"},"PeriodicalIF":3.6000,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0031302524000977/pdfft?md5=fade9799ae330adfbbe74b798282dad0&pid=1-s2.0-S0031302524000977-main.pdf","citationCount":"0","resultStr":"{\"title\":\"A tale of two studies: is peripheral eosinophilia associated with Dientamoeba fragilis detection in adult stool samples?\",\"authors\":\"Priya Garg , John Chetwood , Thuy Phan , Timothy Gray , Genevieve McKew\",\"doi\":\"10.1016/j.pathol.2024.01.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The protozoan parasite <em>Dientamoeba fragilis</em> is a frequently isolated stool organism and postulated cause of gastrointestinal symptoms. Peripheral blood eosinophilia has been described. This is the first study amongst the Australasian adult population to assess the relationship between organism detection and eosinophilia.</p><p>A case-control study took place over 7 years at a single Sydney laboratory site, evaluating patients with <em>D. fragilis</em> identified on stool using real-time PCR with a recent full blood count, to control groups with <em>Giardia</em> spp. and sequential negatives with neither organism. A nested study compared those with microscopic evidence of <em>D. fragilis</em> as a marker of disease burden, to molecular diagnosis alone.</p><p>Sixty-four <em>D. fragilis</em>, 30 <em>Giardia</em> spp., and 94 sequential controls were enrolled. Only 60.1% of samples were preserved in sodium acetate-acetic acid formalin (SAF) fixative, indication mostly not documented. The major co-organism detected amongst all participants was <em>Blastocystis</em> sp., particularly in the <em>D. fragilis</em> cohort (37.2%). The most common pathogen amongst sequential controls was <em>Campylobacter</em> spp. (7.4%). Patients with <em>D. fragilis</em> were more likely (12.5%) to have a clinically significant eosinophilia (>0.5×10<sup>9</sup>/L) compared to those with <em>Giardia</em> spp. (3.3%) or sequential controls (4.3%) (<em>p</em>=0.03). A significant difference was also noted in the overall median eosinophil count of those with <em>D. fragilis</em> versus all controls (0.2 vs 0.1×10<sup>9</sup>/L, <em>p</em>=0.01); however, this was within the reference interval (where up to >0.5×10<sup>9</sup>/L is accepted in healthy individuals within a typical population). No eosinophil difference was found between those with molecular versus additional microscopic detection of <em>D. fragilis</em> (0.1 vs 0.1×10<sup>9</sup>/L).</p><p>These results support an association between the identification of clinically significant peripheral blood eosinophilia and <em>D. fragilis</em> presence, which may impact the diagnostic approach to the patient with unexplained eosinophilia. Further prospective trials may help assess any significance further and the implication of co-carriage with other enteric organisms. The importance of clinical indication and need for appropriate fixative media in diagnostic parasitology are also highlighted.</p></div>\",\"PeriodicalId\":19915,\"journal\":{\"name\":\"Pathology\",\"volume\":\"56 5\",\"pages\":\"Pages 688-695\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0031302524000977/pdfft?md5=fade9799ae330adfbbe74b798282dad0&pid=1-s2.0-S0031302524000977-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0031302524000977\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031302524000977","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PATHOLOGY","Score":null,"Total":0}
A tale of two studies: is peripheral eosinophilia associated with Dientamoeba fragilis detection in adult stool samples?
The protozoan parasite Dientamoeba fragilis is a frequently isolated stool organism and postulated cause of gastrointestinal symptoms. Peripheral blood eosinophilia has been described. This is the first study amongst the Australasian adult population to assess the relationship between organism detection and eosinophilia.
A case-control study took place over 7 years at a single Sydney laboratory site, evaluating patients with D. fragilis identified on stool using real-time PCR with a recent full blood count, to control groups with Giardia spp. and sequential negatives with neither organism. A nested study compared those with microscopic evidence of D. fragilis as a marker of disease burden, to molecular diagnosis alone.
Sixty-four D. fragilis, 30 Giardia spp., and 94 sequential controls were enrolled. Only 60.1% of samples were preserved in sodium acetate-acetic acid formalin (SAF) fixative, indication mostly not documented. The major co-organism detected amongst all participants was Blastocystis sp., particularly in the D. fragilis cohort (37.2%). The most common pathogen amongst sequential controls was Campylobacter spp. (7.4%). Patients with D. fragilis were more likely (12.5%) to have a clinically significant eosinophilia (>0.5×109/L) compared to those with Giardia spp. (3.3%) or sequential controls (4.3%) (p=0.03). A significant difference was also noted in the overall median eosinophil count of those with D. fragilis versus all controls (0.2 vs 0.1×109/L, p=0.01); however, this was within the reference interval (where up to >0.5×109/L is accepted in healthy individuals within a typical population). No eosinophil difference was found between those with molecular versus additional microscopic detection of D. fragilis (0.1 vs 0.1×109/L).
These results support an association between the identification of clinically significant peripheral blood eosinophilia and D. fragilis presence, which may impact the diagnostic approach to the patient with unexplained eosinophilia. Further prospective trials may help assess any significance further and the implication of co-carriage with other enteric organisms. The importance of clinical indication and need for appropriate fixative media in diagnostic parasitology are also highlighted.
期刊介绍:
Published by Elsevier from 2016
Pathology is the official journal of the Royal College of Pathologists of Australasia (RCPA). It is committed to publishing peer-reviewed, original articles related to the science of pathology in its broadest sense, including anatomical pathology, chemical pathology and biochemistry, cytopathology, experimental pathology, forensic pathology and morbid anatomy, genetics, haematology, immunology and immunopathology, microbiology and molecular pathology.