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Familial risk of carpal tunnel syndrome among first-degree relatives and interaction with obesity and hyperglycemia: a population-based study in Korea

Title
Familial risk of carpal tunnel syndrome among first-degree relatives and interaction with obesity and hyperglycemia: a population-based study in Korea
Authors
Kim, Jung Eun; Kim, Bom; Kim, Hyun Jung; Hwang, Jungyun; Swan, Heather; Kim, Young Shin; Cha, Jaewoo; Kang, Taeuk; Kim, Kyoung-Hoon; Kim, Minjung; Hann, Hoo Jae; Kim, Kyeong Uoon; Ahn, Hyeong Sik
Ewha Authors
한후재
SCOPUS Author ID
한후재scopus
Issue Date
2026
Journal Title
PAIN
ISSN
0304-3959JCR Link

1872-6623JCR Link
Citation
PAIN vol. 167, no. 1, pp. 133 - 141
Keywords
Carpal tunnel syndrome; Familial risk; Interaction; Hyperglycemia; Obesity
Publisher
LIPPINCOTT WILLIAMS &

WILKINS
Indexed
SCIE; SCOPUS WOS
Document Type
Article
Abstract
Although genetic and lifestyle factors are known to be involved in carpal tunnel syndrome development, population-level familial risk and interactions between gene and environmental factors have been scarcely studied. We investigated population-based familial risk and assessed the interactions between family history and obesity or hyperglycemia. By using the National Health Insurance database, which covers the total population in Korea, we constructed a cohort of 5,524,403 individuals with information on familial relationships and lifestyle factors from 2002 to 2019. Familial risk was calculated using hazard ratios (HRs) that compare the risk of individuals with and without affected first-degree relatives (FDRs). Interactions between familial risk and obesity/hyperglycemia were assessed on an additive scale using the relative excess risk due to interaction (RERI). Individuals with affected FDRs showed a 1.99-fold increased risk of disease, with twin, brother, sister, paternal, and maternal risks (95% confidence interval) of 17.53 (9.43-32.58), 2.57 (2.20-3.00), 2.38 (2.04-2.77), 1.72 (1.60-1.86), and 1.95 (1.88-2.03), respectively. In the interaction analysis, the combined risk of positive family history and high body mass index or hyperglycemia exceeded the sum of their individual risks (HR 3.33 vs 2.55, 2.51 vs 2.28, respectively), showing statistically significant interactions (RERI 0.78, 0.23, respectively). Obese individuals with a family history (RERI 1.12) showed a more prominent interaction than overweight individuals (RERI 0.26), and similarly, excess risk was higher in severe hyperglycemic (RERI 0.82) compared with moderate hyperglycemic individuals (RERI 0.28), suggesting a dose-response interaction pattern. Our interaction findings indicate that individuals with a family history and obesity/hyperglycemia should be considered a high-risk population.
DOI
10.1097/j.pain.0000000000003757
Appears in Collections:
의과대학 > 의학과 > Journal papers
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