| Title: | LDLR and APOB pathogenic variants predict discordant TSH effect on LDL-C |
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| Authors: | ID Kafol, Jan (Author)
ID Šikonja, Jaka (Author)
ID Mlinarič, Matej (Author)
ID Čugalj Kern, Barbara (Author)
ID Pricop-Jeckstadt, Mihaela (Author)
ID Drole Torkar, Ana (Author)
ID Gorjanc, Tevž (Author)
ID Petek, Andraž (Author)
ID Lakner, Andreja (Author)
ID Kovač, Jernej (Author)
ID Battelino, Tadej (Author)
ID Grošelj, Urh (Author) |
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| Files: |  PDF - Presentation file, download (2,39 MB)
MD5: 7FED8CBA40B74CA236A67E60AA9EF8CD
 URL - Source URL, visit https://www.atherosclerosis-journal.com/article/S0021-9150(26)00038-9/fulltext
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| Language: | English |
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| Typology: | 1.01 - Original Scientific Article |
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| Organization: |  UKC LJ - Ljubljana University Medical Centre
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| Abstract: | Background and aims Thyroid hormones regulate lipoprotein metabolism—primarily by up-regulating the LDL receptor. Whether TSH relates to LDL-C in hypercholesterolemic children, and whether this depends on familial hypercholesterolemia (FH) status or the underlying defective gene, is uncertain. We evaluated TSH–lipid associations in prepubertal children and tested effect modification by FH status and, within FH, by gene with a pathogenic variant (LDLR vs APOB). Methods We performed a cross-sectional study of prepubertal children referred to the Slovenian national tertiary center through the universal FH screening program or cascade screening. Eligibility required concurrent TSH and fasting lipid measurement and completed genetic testing (pathogenic/likely pathogenic variants in LDLR/APOB/PCSK9 vs polygenic hypercholesterolemia). Results Among 738 children, 182 (24.7%) were FH-positive (LDLR 132; APOB 50). In the pooled cohort, TSH did not correlate with age or lipids (all p≥0.050). After sex stratification, TSH correlated with triglycerides only in males (ρ=0.156; p=0.012). In FH-positive children, TSH correlated with total cholesterol, LDL-cholesterol, and ApoB (ρ≈0.184–0.207; all p<0.050), with no associations in FH-negative children. Interaction testing confirmed effect modification by FH (TSH×FH β=0.141 mmol/L per mIU/L, p=0.023). Within FH-positive children, a positive TSH–LDL-C slope was seen in LDLR carriers (β=0.237, p=0.004) but not in APOB carriers (β=−0.065, p=0.655). Conclusions TSH was positively associated with LDL-C only in FH due to LDLR variants, not in APOB carriers. These findings suggest that genetic background may shape hormonal sensitivity, and that attention to thyroid status could be particularly relevant in LDLR-FH. |
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| Keywords: | TSH, low-density lipoprotein cholesterol, familial hypercholesterolemia, LDLR, APOB, subclinical hypothyroidism |
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| Publication status: | Published |
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| Publication version: | Version of Record |
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| Year of publishing: | 2026 |
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| Number of pages: | str. 1-7 |
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| Numbering: | Vol. 415, [article no.] 120672 |
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| PID: | 20.500.12556/DiRROS-28368  |
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| UDC: | 616.1:616-053.2 |
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| ISSN on article: | 1879-1484 |
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| DOI: | 10.1016/j.atherosclerosis.2026.120672 |
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| COBISS.SI-ID: | 268549379 |
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| Note: | Nasl. z nasl. zaslona;
Opis vira z dne 16. 2. 2026; |
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| Publication date in DiRROS: | 16.03.2026 |
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| Views: | 102 |
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| Downloads: | 53 |
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