Objective: The French medico-historical literature reports the common use of mercury-based treatments until the mid-19th century. An exploratory paleopharmacological approach is presented for detecting mercury in a child's skeletal remains suffering from vitamin deficiencies. This aims to corroborate written sources and provide a way to better understand disease therapeutic management.
Materials: This study focuses on a 3-4-year-old child showing signs of rickets and possible scurvy from "rue Thubeuf" cemetery (Rouen, late 18-19th centuries). Analysis was carried out on a thoracic vertebral body and the right second deciduous mandibular molar.
Methods: Energy dispersive X-ray fluorescence (ED-XRF) and cold vapor atomic absorption spectroscopy (CV-AAS) provided mercury detection and quantification. Micro-CT analysis was implemented to detect the interglobular dentine potentially related to vitamin D deficiency.
Results: The ED-XRF spectrum showed a mercury peak for the vertebra, none for the molar. The vertebra CV-AAS analysis revealed a high mercury rate of 9.373 mg/kg.
Conclusions: The individual was likely exposed to high mercury levels originating from therapeutic treatment, potentially for vitamin deficiencies, in the last months of life.
Significance: Paleopharmacological analysis is an important tool in the analysis of medical treatment in the past.
Limitations: Soil analysis could contribute to improved knowledge of contamination sources.
Further Research: This approach should be expanded to more individuals to better assess the treatment frequency of vitamin deficiency diseases during industrialization.
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http://dx.doi.org/10.1016/j.ijpp.2025.02.006 | DOI Listing |
BMJ Open
March 2025
Department of Medicine, University of Ibadan, Ibadan, Oyo, Nigeria.
Objectives: To investigate homocysteine (Hcy) levels in individuals with chronic kidney disease (CKD), hypertension and a healthy Nigerian population, and to assess their association with cardiovascular disease (CVD) risk.
Setting: The study was conducted using data from the Ibadan CRECKID (Cardiovascular and Renal Event in People with Chronic Kidney Disease) study in Nigeria.
Participants: A total of 420 adults (aged 18+) categorised into three groups: individuals with stage 2 CKD or higher, hypertensive non-CKD individuals and normotensive individuals.
Forensic Sci Med Pathol
March 2025
Forensic Medicine Department, Dijon Teaching Hospital, Dijon, France.
Fictitious disorder by proxy (FDP) is characterized by an adult, often a parent, alleging or fabricating symptoms in a child to induce repeated diagnostic tests or treatments. This form of abuse is particularly serious and difficult to diagnose. Worldwide, it is estimated that 0.
View Article and Find Full Text PDFCurr Nutr Rep
March 2025
Departamento de Investigación y Desarrollo, Good Research and Science (GRS), Avenida Ramón Picarte 780, 5090000, Valdivia, Chile.
Purpose Of Review: Veganism, characterized by the exclusion of all animal-derived products, has grown in popularity due to ethical, environmental, and health considerations. However, vegan athletes often face unique nutritional challenges related to dietary deficiencies of critical nutrients such as proteins, vitamin B12, iron, calcium, and omega-3 fatty acids, among others. This narrative review aims to explore the efficacy and benefits of vegan-friendly supplements specifically tailored to athletic performance, focusing on essential micronutrients, ergogenic aids, and nutrient bioavailability.
View Article and Find Full Text PDFJ Cutan Med Surg
March 2025
Division of Dermatology, University of Alberta, Edmonton, AB, Canada.
Calcinosis cutis, characterized by the pathological deposition of insoluble calcium salts in the skin, is associated with several disease entities, particularly autoimmune conditions such as scleroderma and dermatomyositis. Lesions of calcinosis are often painful, prone to ulceration, and significantly impair quality of life. Despite the clinical impact, no effective treatments have been established to date, making prevention of this condition a critical priority.
View Article and Find Full Text PDFEndokrynol Pol
March 2025
Department of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi, China.
Introduction: Thiamine-responsive megaloblastic anaemia syndrome (TRMA) is a rare genetic disease caused by mutations in the SLC19A2 gene that encodes thiamine transporter 1 (THTR-1). The common manifestations are diabetes, anaemia, and deafness. The pathogenic mechanism has not yet been clarified.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!