TY - JOUR
T1 - Real-world data on vitamin D supplementation and its impacts in systemic lupus erythematosus
T2 - Cross-sectional analysis of a lupus registry of nationwide institutions (LUNA)
AU - Hayashi, Keigo
AU - Sada, Kenei
AU - Asano, Yosuke
AU - Katayama, Yu
AU - Ohashi, Keiji
AU - Morishita, Michiko
AU - Miyawaki, Yoshia
AU - Watanabe, Haruki
AU - Katsuyama, Takayuki
AU - Narazaki, Mariko
AU - Matsumoto, Yoshinori
AU - Yajima, Nobuyuki
AU - Yoshimi, Ryusuke
AU - Shimojima, Yasuhiro
AU - Ohno, Shigeru
AU - Kajiyama, Hiroshi
AU - Ichinose, Kunihiro
AU - Sato, Shuzo
AU - Fujiwara, Michio
AU - Wada, Jun
N1 - Publisher Copyright:
© 2022 Hayashi et al
PY - 2022/6
Y1 - 2022/6
N2 - Background Although vitamin D concentration is reportedly associated with the pathogenesis and pathology of systemic lupus erythematosus (SLE), benefits of vitamin D supplementation in SLE patients have not been elucidated, to our knowledge. We investigated the clinical impacts of vitamin D supplementation in SLE. Methods A cross-sectional analysis was performed using data from a lupus registry of nationwide institutions. We evaluated vitamin D supplementation status associated with diseaserelated Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI) as a parameter of long-term disease activity control. Results Of the enrolled 870 patients (mean age: 45 years, mean disease duration: 153 months), 426 (49%) received vitamin D supplementation. Patients with vitamin D supplementation were younger (43.2 vs 47.5 years, P 0.0001), received higher doses of prednisolone (7.6 vs 6.8 mg/day, P = 0.002), and showed higher estimated glomerular filtration rates (79.3 vs 75.3 mL/min/1.73m2, P = 0.02) than those without supplementation. Disease-related SDI (0.73 ± 1.12 vs 0.73 ± 1.10, P = 0.75), total SDI, and SLE Disease Activity Index (SLEDAI) did not significantly differ between patients receiving and not receiving vitamin D supplementation. Even after excluding 136 patients who were highly recommended vitamin D supplementation (with age 75 years, history of bone fracture or avascular necrosis, denosumab use, and end-stage renal failure), disease-related SDI, total SDI, and SLEDAI did not significantly differ between the two groups. Conclusions Even with a possible Vitamin D deficiency and a high risk of bone fractures in SLE patients, only half of our cohort received its supplementation. The effect of vitamin D supplementation for disease activity control was not observed.
AB - Background Although vitamin D concentration is reportedly associated with the pathogenesis and pathology of systemic lupus erythematosus (SLE), benefits of vitamin D supplementation in SLE patients have not been elucidated, to our knowledge. We investigated the clinical impacts of vitamin D supplementation in SLE. Methods A cross-sectional analysis was performed using data from a lupus registry of nationwide institutions. We evaluated vitamin D supplementation status associated with diseaserelated Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI) as a parameter of long-term disease activity control. Results Of the enrolled 870 patients (mean age: 45 years, mean disease duration: 153 months), 426 (49%) received vitamin D supplementation. Patients with vitamin D supplementation were younger (43.2 vs 47.5 years, P 0.0001), received higher doses of prednisolone (7.6 vs 6.8 mg/day, P = 0.002), and showed higher estimated glomerular filtration rates (79.3 vs 75.3 mL/min/1.73m2, P = 0.02) than those without supplementation. Disease-related SDI (0.73 ± 1.12 vs 0.73 ± 1.10, P = 0.75), total SDI, and SLE Disease Activity Index (SLEDAI) did not significantly differ between patients receiving and not receiving vitamin D supplementation. Even after excluding 136 patients who were highly recommended vitamin D supplementation (with age 75 years, history of bone fracture or avascular necrosis, denosumab use, and end-stage renal failure), disease-related SDI, total SDI, and SLEDAI did not significantly differ between the two groups. Conclusions Even with a possible Vitamin D deficiency and a high risk of bone fractures in SLE patients, only half of our cohort received its supplementation. The effect of vitamin D supplementation for disease activity control was not observed.
UR - http://www.scopus.com/inward/record.url?scp=85133214896&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85133214896&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0270569
DO - 10.1371/journal.pone.0270569
M3 - Article
C2 - 35767524
AN - SCOPUS:85133214896
SN - 1932-6203
VL - 17
JO - PLoS One
JF - PLoS One
IS - 6 June
M1 - e0270569
ER -