Osteoporosis & bone health

The role of the CYP1A1 gene in long-term glucocorticoid-related adverse effects

Osteoporos IntPublished Genotyping study of CYP1A1 variants in patients on chronic glucocorticoid (GC) treatment

Authors' conclusion

The CYP1A1 rs1799814 polymorphism is associated with more severe GC-related AE, suggesting reduced GC metabolism.

Study context

Population
Patients receiving chronic GC treatment (≥5 mg/day for >3 months) (56 ± 16.6 years; 71.4% female; 47.1% postmenopausal)patients receiving chronic GC treatment included
Participants
70 patients
Comparison
Patients with vs without the CYP1A1 rs1799814 polymorphism
  • rs1799814 polymorphismn = nine
Outcome
CYP1A1 polymorphisms identified
Methodological details5 years of follow-up, CYP1A1 gene sequencing by NGS using Amplicon Deep Sequencing on an Ion Torrent platform
  • 5 years of follow-up
  • CYP1A1 gene sequencing by NGS using Amplicon Deep Sequencing on an Ion Torrent platform

Main finding

As reported in the abstract

rs1048943
Nine patients
rs1799814
nine
rs4646422
one
rs41279188
one

Further findings

NTx · lower with rs1799814

P = 0.003

CTx

P = 0.068

OC

P = 0.059

Outcomers1799814 polymorphismWithout rs1799814P value
BMIHigher BMI with rs179981429.325.5P = 0.019
BMI change (ΔBMI) · 5 yearsGreater BMI change with rs1799814 · adjusted for cumulative GC dose1.7−0.32P = 0.02

Osteoporosis and/or fractures, bone mineral density (BMD) or trabecular bone score (TBS) values

No associations were found between CYP1A1 polymorphisms and the presence of osteoporosis and/or fractures, BMD or TBS values

Original publication

The role of the CYP1A1 gene in long-term glucocorticoid-related adverse effects. Osteoporos Int. Published 27 October 2026. doi:10.1007/s00198-026-08253-6

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