Association of a polygenic risk score with low trauma fractures in people with HIV - The swiss HIV cohort study.
Publisher DOI
PubMed ID
41671232
Abstract
Background
Polygenic risk scores (PRS) are likely to enter routine clinical care for individual disease risk prediction in the next 10 years. We recently showed that the bone mineral density-associated gSOS-PRS is independently associated with a > 4-fold increased risk of osteoporosis in the Swiss HIV Cohort Study (SHCS). Here we investigate whether this PRS is also associated with low trauma fractures (LTF) in people with HIV in the SHCS.Methods
Applying a case-control design, cases had a first LTF (1994-2022) and LTF-free controls were matched on age, sex and observation time. We obtained univariable odds ratios (OR) for LTF in SHCS participants of European descent, based on a genome-wide PRS built from 9413 LTF-associated single nucleotide polymorphisms (SNPs). In multivariable analysis, LTF odds ratios of the PRS were adjusted for non-genetic (traditional and HIV-related) LTF risk factor profile including potentially adverse antiretroviral exposures.Results
We included 277 SHCS participants with a first LTF (cases) and 796 LTF-free controls (median age 55 years; 68% male; 91% with suppressed HIV RNA). Participants with the most unfavorable genetic background (top quintile of the gSOS-PRS) had univariable and multivariable LTF-OR of 2.30 (95% confidence interval, 1.49-3.56) and 2.30 (1.43-3.72), respectively, compared to participants with the most favorable genetic background (bottom gSOS-PRS quintile). Participants with the most unfavorable non-genetic risk factor profile (top quintile) had an adjusted gSOS-OR of 7.42 (95% confidence interval [CI], 4.3-12.82), compared with participants in the bottom quintile.Conclusions
In people with HIV in Switzerland, an unfavorable PRS was independently associated with LTF risk after adjustment for traditional and HIV-related LTF risk factors.
Polygenic risk scores (PRS) are likely to enter routine clinical care for individual disease risk prediction in the next 10 years. We recently showed that the bone mineral density-associated gSOS-PRS is independently associated with a > 4-fold increased risk of osteoporosis in the Swiss HIV Cohort Study (SHCS). Here we investigate whether this PRS is also associated with low trauma fractures (LTF) in people with HIV in the SHCS.Methods
Applying a case-control design, cases had a first LTF (1994-2022) and LTF-free controls were matched on age, sex and observation time. We obtained univariable odds ratios (OR) for LTF in SHCS participants of European descent, based on a genome-wide PRS built from 9413 LTF-associated single nucleotide polymorphisms (SNPs). In multivariable analysis, LTF odds ratios of the PRS were adjusted for non-genetic (traditional and HIV-related) LTF risk factor profile including potentially adverse antiretroviral exposures.Results
We included 277 SHCS participants with a first LTF (cases) and 796 LTF-free controls (median age 55 years; 68% male; 91% with suppressed HIV RNA). Participants with the most unfavorable genetic background (top quintile of the gSOS-PRS) had univariable and multivariable LTF-OR of 2.30 (95% confidence interval, 1.49-3.56) and 2.30 (1.43-3.72), respectively, compared to participants with the most favorable genetic background (bottom gSOS-PRS quintile). Participants with the most unfavorable non-genetic risk factor profile (top quintile) had an adjusted gSOS-OR of 7.42 (95% confidence interval [CI], 4.3-12.82), compared with participants in the bottom quintile.Conclusions
In people with HIV in Switzerland, an unfavorable PRS was independently associated with LTF risk after adjustment for traditional and HIV-related LTF risk factors.
Date Issued
2026
Publication Type
Article
Subject(s)
Language(s)
en
Author(s)
Strickler, Claudio | |
Thorball, Christian W | |
Schwenke, Johannes | |
Hasse, Barbara | |
Ryom, Lene | |
Kahlert, Christian R | |
Bernasconi, Enos | |
Calmy, Alexandra | |
Lamy, Olivier | |
Günthard, Huldrych F | |
Ledergerber, Bruno | |
Tarr, Philip E |
Journal
PLoS ONE
Publisher
Public Library of Science
ISSN
1932-6203
Access(Rights)
open.access