Background There are no available lifetime risk estimates of lower-extremity peripheral artery disease (PAD). Methods and Results Using data from 6 US community-based cohorts and the vital statistics, we estimated the prevalence and incidence of PAD, defined as an ankle-brachial index < 0.90, at each year of age from birth to 80 years for white, black, and Hispanic men and women. Then, we used Markov Monte Carlo simulations in a simulated cohort of 100 000 individuals to estimate lifetime risk of PAD. On the basis of odds ratios of PAD for traditional atherosclerotic risk factors (eg, diabetes mellitus and smoking), we developed a calculator providing residual lifetime risk of PAD. In an 80-year horizon, lifetime risks of PAD were 30.0% in black men and 27.6% in black women, but ≈19% in white men and women and ≈22% in Hispanic men and women. From another perspective, 9% of blacks were estimated to develop PAD by 60 years of age, while the same proportion was seen at ≈70 years for whites and Hispanics. The residual lifetime risk within the same race/ethnicity varied by 3.5- to 5-fold according to risk factors (eg, residual lifetime risk in 45-year-old black men was 19.9% when current smoking, diabetes mellitus, and history of cardiovascular disease were absent versus 70.4% when all were present). Conclusions In the United States, ≈30% of blacks are estimated to develop PAD during their lifetime, whereas the corresponding estimate is ≈20% for whites and Hispanics. The residual lifetime risk within the same race/ethnicity substantially varies according to traditional risk factors.
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http://dx.doi.org/10.1161/JAHA.119.012177 | DOI Listing |
Isotopes Environ Health Stud
March 2025
Department of Materials and Material processing, Vocational School of Technical Sciences, Kahramanmaras Sutcu Imam University, K. Maras, Turkey.
This research aimed to measure radon activity concentrations in bottled drinking water (BDW) samples consumed in Kahramanmaraş town, Turkiye. Also, to evaluate the health risk that may occur as a result of internal irradiation resulting from ingestion and inhalation of radon in BDW samples, the total annual effective dose equivalent (AEDE) for infants, children, and adults (1-2 y, 2-12 y, and > 17 y) and excess lifetime cancer risk (ELCR) for adults (> 17 y) had to be calculated. For these purposes, 32 water samples of different volumes belonging to 8 different commercial brands, representing a large part of the BDW consumed as drinking water and sold commercially in Kahramanmaraş were collected by purchasing from markets.
View Article and Find Full Text PDFOrthop J Sports Med
March 2025
Department of Orthopedic Surgery, Orthopedic and Arthritis Center for Outcomes Research, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Background: Understanding the factors contributing to willingness to participate in randomized clinical trials (RCTs) after anterior cruciate ligament reconstruction (ACLR) is crucial to optimizing recruitment and understanding whether interested participants represent the patient population that may benefit from the studied treatment.
Purpose: To understand patients' willingness to participate in a future RCT of an oral medication to prevent posttraumatic osteoarthritis (PTOA) after ACLR.
Study Design: Cross-sectional study; Level of evidence, 3.
J Environ Health Sci Eng
June 2025
Department of Nutrition and Food Hygiene, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Trihalomethanes (THMs) are a class of compounds formed when organic substances in water interact with halogen disinfectants such as chlorine. The specific THMs include CHBr, CHClBr, CHClBr, and CHCl. THMs are toxic disinfection by-products (DBPs) that pose potential risks to human health and can be present in ready-to-eat vegetables.
View Article and Find Full Text PDFInt J Mol Sci
February 2025
Thrombosis Research Group (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, 9019 Tromsø, Norway.
MicroRNA-145-5p (miR-145) has been reported to regulate multiple oncogenes and is considered a tumor suppressor. However, it remains unknown whether the level of plasma miR-145 can serve as a risk biomarker for future cancer. Using a population-based cohort ( = 1740) derived from the Trøndelag Health Study (HUNT), we investigated whether plasma miR-145 levels were associated with (1) first life-time cancer, (2) cancer stage at diagnosis, and (3) 2-year all-cause mortality after cancer diagnosis.
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