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Polymorphic Variants in the Vitamin D Receptor and Clinical Parameters of Rheumatoid Arthritis Patients Undergoing Anti-TNF Treatment

Open Access
|Nov 2024

Figures & Tables

Fig 1.

Differences in CRP and VAS parameters in relation to VDR rs1544410 genotypes (Mann–Whitney test). Data are presented as median with IQR. CRP, C-reactive protein; IQRs, interquartile ranges; VAS, visual analog scale; VDR, vitamin D receptor.
Differences in CRP and VAS parameters in relation to VDR rs1544410 genotypes (Mann–Whitney test). Data are presented as median with IQR. CRP, C-reactive protein; IQRs, interquartile ranges; VAS, visual analog scale; VDR, vitamin D receptor.

Fig 2.

Differences in CRP and VAS parameters in relation to VDR rs731236 genotypes (Mann–Whitney test). Data are presented as median with IQR. CRP, C-reactive protein; IQRs, interquartile ranges; VAS, visual analog scale; VDR, vitamin D receptor.
Differences in CRP and VAS parameters in relation to VDR rs731236 genotypes (Mann–Whitney test). Data are presented as median with IQR. CRP, C-reactive protein; IQRs, interquartile ranges; VAS, visual analog scale; VDR, vitamin D receptor.

Fig 3.

Differences in the levels of 25(OH)D3 level (ng/mL) according to the presence of VDR genotypes: rs2228570 (ordinary one-way ANOVA, p = 0.014) and rs797532 (Kruskal–Wallis test, p = 0.008). 25(OH)D3, 25-hydroxyvitamin D3; VDR, vitamin D receptor.
Differences in the levels of 25(OH)D3 level (ng/mL) according to the presence of VDR genotypes: rs2228570 (ordinary one-way ANOVA, p = 0.014) and rs797532 (Kruskal–Wallis test, p = 0.008). 25(OH)D3, 25-hydroxyvitamin D3; VDR, vitamin D receptor.

Characteristics of patients’ subgroup

Calcium (mg/dL)Alkaline phosphatase (U/L)Vitamin D3 (ng/mL)TSH (ulU/mL)
N56645464
Minimum8.9364.640.271
Median9.774.523.671.201
Maximum10.7350664.331
IQR0.533.2523.140.744

Characteristics of the RA patients included in the study

Number of patients121
Age mean in years (±SD)52.2 (13.3)
Disease duration mean in years (±SD)13.6 (9.31)
Disease onset mean in years (±SD)38.6 (14.0)
Sex F/M (%)96/25 (79.3)
BMI mean (±SD)25.7 (4.69)
RF-positive patients (%)86.7
Anti-CCP positive patients (%)82.4
Anti-TNF drugs:N (%)
Adalimumab41 (33.9)
Etanercept48 (39.7)
Certolizumab pegol19 (15.7)
Golimumab9 (7.44)
Infliximab4 (3.31)
Concomitant treatment at the start of biologic treatment(%)
NSAIDs73.2
MTX83.6
Corticosteroids82.1
Disease activity:
DAS28 before treatment, mean (±SD)6.14 (0.713)
DAS28 after 6 months of treatment, mean (±SD)2.63 (0.939)

Relationships between VDR rs7975232 genetic variants and vitamin D levels in RA patients

VDR rs797523225(OH)D3 conc. (ng/mL)
Median (IQR)AA29.6 (25.34)
AC + CC21.54 (21.2)
AA + AC21.54 (17.02)
CC36.68 (19.87)
AA + CC33.33 (20.81)
AC19.32 (12.56)
Mann–Whitney test p-valuesAA vs. AC + CC0.1703
AA + AC vs. CC0.029
AA + CC vs. AC0.003
AA vs. AC0.021
AC vs. CC0.009
AA vs. CC0.324

VDR genotype and minor allele frequencies of RA patients and control group

GenotypesMAFχ2χ2 p-value

SNPRAControlsRAControlsRAControlsRAControls1000 genomes project–CEURAControlsRAControls

rs1544410AA AG GG 0.3680.4340.4700.4082.1460.5230.143
182753525043
rs2228570CC CT TT 0.4380.4220.4290.0060.4170.9370.518
383960632320
rs731236CC CT TT 0.3600.4090.4000.8692.9200.3510.087
181551655236
rs7975232AA AC CC 0.4830.4960.4040.0681.6920.7940.193
332659652925

Relationships between VDR rs2228570 genetic variants and vitamin D levels in RA patients

VDR rs222857025(OH)D3 conc. (ng/mL)
Mean (±SD)CC20.69 ± 11.12
CT32.22 ± 16.06
TT22.33 ± 9.077
Median (IQR)CC18.47 (16.98)
CT + TT25.08 (22.07)
CC + CT23.88 (24.48)
TT21.54 (14.92)
p-valuesCC vs. CT + TT0.028
CC + CT vs. TT0.508
CC + TT vs. CT0.004
CC vs. CT0.009
CT vs. TT0.093
CC vs. TT0.701
Language: English
Submitted on: Jun 28, 2024
Accepted on: Oct 18, 2024
Published on: Nov 10, 2024
Published by: Hirszfeld Institute of Immunology and Experimental Therapy
In partnership with: Paradigm Publishing Services
Publication frequency: 1 times per year

© 2024 Joanna Wielińska, Katarzyna Górna, Jerzy Świerkot, Bartosz Bugaj, Katarzyna Kolossa, Sławomir Jeka, Katarzyna Bogunia-Kubik, published by Hirszfeld Institute of Immunology and Experimental Therapy
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.