ESR1 Gene Variants Are Predictive of Osteoporosis in Female Patients with Crohn's Disease.
Iwona Krela-KaźmierczakMarzena Skrzypczak-ZielinskaIwona Krela-KaźmierczakMichał MichalakAleksandra Szymczak-TomczakSzymon T HryhorowiczMarlena SzalataLiliana Łykowska-SzuberPiotr EderKamila Stawczyk-EderMaciej TomczakRyszard SlomskiAgnieszka DobrowolskaPublished in: Journal of clinical medicine (2019)
Decreased bone mass in patients with inflammatory bowel diseases (IBD) is a clinical problem with extremely severe consequences of osteoporotic fractures. Despite its increasing prevalence and the need for mandatory intervention and monitoring, it is often ignored in IBD patients' care. Determining the biomarkers of susceptibility to bone mineral density disorder in IBD patients appears to be indispensable. We aim to investigate the impact of estrogen receptor gene (ESR1) gene polymorphisms on bone mineral density (BMD) in patients with ulcerative colitis (UC) and Crohn's disease (CD), as they may contribute both, to osteoporosis and inflammatory processes. We characterised 197 patients with IBD (97 with UC, 100 with CD), and 41 controls carrying out vitamin D, calcium and phosphorus serum levels, and bone mineral density assessment at the lumbar spine and the femoral neck by dual-energy X-ray absorptiometry (DXA), ESR1 genotyping and haplotype analysis. We observed that women with CD showed the lowest bone density parameters, which corresponded to the ESR1 c.454-397T and c.454-351A allele dose. The ESR1 gene PvuII and XbaI TA (px) haplotype correlated with decreased femoral neck T-score (OR = 2.75, CI = [1.21-6.27], P-value = 0.016) and may be predictive of osteoporosis in female patients with CD.
Keyphrases
- bone mineral density
- postmenopausal women
- estrogen receptor
- body composition
- ulcerative colitis
- end stage renal disease
- dual energy
- ejection fraction
- copy number
- newly diagnosed
- chronic kidney disease
- genome wide
- randomized controlled trial
- computed tomography
- healthcare
- peritoneal dialysis
- prognostic factors
- nk cells
- dna methylation
- magnetic resonance imaging
- risk factors
- risk assessment
- mass spectrometry
- quality improvement
- patient reported outcomes
- single cell
- pain management
- chronic pain
- contrast enhanced
- drug induced
- genome wide analysis