{"title":"19至20世纪瑞士里吉斯堡济贫院墓地的地方性先天性缺碘综合症","authors":"Christine Cooper , Florian Keller , Amelie Alterauge , Sandra Lösch","doi":"10.1016/j.ijpp.2025.06.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To identify and describe skeletal remains showing features consistent with congenital iodine deficiency syndrome (CIDS), also known as \"cretinism\" and to explore whether this condition may have been underdiagnosed or if it is underrepresented in archaeological skeletal assemblages.</div></div><div><h3>Materials</h3><div>121 adult skeletons from the 19th/20th century former Riggisberg poorhouse cemetery.</div></div><div><h3>Methods</h3><div>The remains were studied macroscopically using standard osteological methods for the estimation of age, sex and stature.</div></div><div><h3>Results</h3><div>Features typical of CIDS were detected in four individuals, and for another six, we consider it a highly consistent diagnosis. The review of palaeopathological data from a comparative sample of 2314 archaeological skeletons revealed an underrepresentation of individuals with CIDS but also clues that previously undiagnosed cases may exist.</div></div><div><h3>Conclusions</h3><div>We suggest that an underrepresentation in the archaeological record of endemic regions may be due to increased childhood mortality of affected individuals, difficulties in diagnosing this condition in immature skeletal remains, and – at least in the modern period – frequent institutionalization and burial in specific cemeteries belonging the institutions.</div></div><div><h3>Significance</h3><div>Several new cases of CIDS increase the small body of known affected remains and add to the knowledge about its skeletal manifestations. This study contributes to the differential diagnosis of a nearly eradicated disease and to its assessment in past populations.</div></div><div><h3>Limitations</h3><div>Incompletely preserved skeletons limited the assessment and diagnosis.</div></div><div><h3>Suggestions for further research</h3><div>Further intensive review and precise assessment of skeletons is advised to explain archaeological underrepresentation of diseases.</div></div>","PeriodicalId":48817,"journal":{"name":"International Journal of Paleopathology","volume":"50 ","pages":"Pages 44-56"},"PeriodicalIF":1.3000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Endemic congenital iodine deficiency syndrome from a 19th to 20th century poorhouse cemetery in Riggisberg, Switzerland\",\"authors\":\"Christine Cooper , Florian Keller , Amelie Alterauge , Sandra Lösch\",\"doi\":\"10.1016/j.ijpp.2025.06.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>To identify and describe skeletal remains showing features consistent with congenital iodine deficiency syndrome (CIDS), also known as \\\"cretinism\\\" and to explore whether this condition may have been underdiagnosed or if it is underrepresented in archaeological skeletal assemblages.</div></div><div><h3>Materials</h3><div>121 adult skeletons from the 19th/20th century former Riggisberg poorhouse cemetery.</div></div><div><h3>Methods</h3><div>The remains were studied macroscopically using standard osteological methods for the estimation of age, sex and stature.</div></div><div><h3>Results</h3><div>Features typical of CIDS were detected in four individuals, and for another six, we consider it a highly consistent diagnosis. The review of palaeopathological data from a comparative sample of 2314 archaeological skeletons revealed an underrepresentation of individuals with CIDS but also clues that previously undiagnosed cases may exist.</div></div><div><h3>Conclusions</h3><div>We suggest that an underrepresentation in the archaeological record of endemic regions may be due to increased childhood mortality of affected individuals, difficulties in diagnosing this condition in immature skeletal remains, and – at least in the modern period – frequent institutionalization and burial in specific cemeteries belonging the institutions.</div></div><div><h3>Significance</h3><div>Several new cases of CIDS increase the small body of known affected remains and add to the knowledge about its skeletal manifestations. This study contributes to the differential diagnosis of a nearly eradicated disease and to its assessment in past populations.</div></div><div><h3>Limitations</h3><div>Incompletely preserved skeletons limited the assessment and diagnosis.</div></div><div><h3>Suggestions for further research</h3><div>Further intensive review and precise assessment of skeletons is advised to explain archaeological underrepresentation of diseases.</div></div>\",\"PeriodicalId\":48817,\"journal\":{\"name\":\"International Journal of Paleopathology\",\"volume\":\"50 \",\"pages\":\"Pages 44-56\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Paleopathology\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1879981725000361\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"PALEONTOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Paleopathology","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1879981725000361","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PALEONTOLOGY","Score":null,"Total":0}
Endemic congenital iodine deficiency syndrome from a 19th to 20th century poorhouse cemetery in Riggisberg, Switzerland
Objective
To identify and describe skeletal remains showing features consistent with congenital iodine deficiency syndrome (CIDS), also known as "cretinism" and to explore whether this condition may have been underdiagnosed or if it is underrepresented in archaeological skeletal assemblages.
Materials
121 adult skeletons from the 19th/20th century former Riggisberg poorhouse cemetery.
Methods
The remains were studied macroscopically using standard osteological methods for the estimation of age, sex and stature.
Results
Features typical of CIDS were detected in four individuals, and for another six, we consider it a highly consistent diagnosis. The review of palaeopathological data from a comparative sample of 2314 archaeological skeletons revealed an underrepresentation of individuals with CIDS but also clues that previously undiagnosed cases may exist.
Conclusions
We suggest that an underrepresentation in the archaeological record of endemic regions may be due to increased childhood mortality of affected individuals, difficulties in diagnosing this condition in immature skeletal remains, and – at least in the modern period – frequent institutionalization and burial in specific cemeteries belonging the institutions.
Significance
Several new cases of CIDS increase the small body of known affected remains and add to the knowledge about its skeletal manifestations. This study contributes to the differential diagnosis of a nearly eradicated disease and to its assessment in past populations.
Limitations
Incompletely preserved skeletons limited the assessment and diagnosis.
Suggestions for further research
Further intensive review and precise assessment of skeletons is advised to explain archaeological underrepresentation of diseases.
期刊介绍:
Paleopathology is the study and application of methods and techniques for investigating diseases and related conditions from skeletal and soft tissue remains. The International Journal of Paleopathology (IJPP) will publish original and significant articles on human and animal (including hominids) disease, based upon the study of physical remains, including osseous, dental, and preserved soft tissues at a range of methodological levels, from direct observation to molecular, chemical, histological and radiographic analysis. Discussion of ways in which these methods can be applied to the reconstruction of health, disease and life histories in the past is central to the discipline, so the journal would also encourage papers covering interpretive and theoretical issues, and those that place the study of disease at the centre of a bioarchaeological or biocultural approach. Papers dealing with historical evidence relating to disease in the past (rather than history of medicine) will also be published. The journal will also accept significant studies that applied previously developed techniques to new materials, setting the research in the context of current debates on past human and animal health.