Universidade Federal do Paraná, Curitiba, Brazil.
Clinical Laboratory Unit, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.
Osteoporos Int. 2018 Feb;29(2):433-440. doi: 10.1007/s00198-017-4299-2. Epub 2017 Nov 15.
This study evaluated the number of comorbidities between two normal values of 25OHD in outpatients during 1 year of 25OHD measurements. Five hundred twenty-nine outpatients were included, patients with 25OHD ≥ 20 and < 30 ng/mL had the higher number of comorbidities, suggesting that for this specific population, 25OHD ≥ 30 ng/mL would be more appropriate. INTRODUCTION : This study evaluated the comorbidities between two values of 25OHD in outpatients of a tertiary hospital.
This is a cross-sectional study with measures of 25OHD in 1-year period, excluding 25OHD < 20 and > 50 ng/mL, clinical research participants, and liver disease and chronic renal failure patients. Patients were divided into two groups: group 1 (G1), 25OHD ≥ 20 and < 30 ng/mL; and group 2 (G2), 250HD ≥ 30 and ≤ 50 ng/mL. Medical records were reviewed for demographic, laboratory, and comorbidity data.
From 529 outpatients included, 319 were in G1 (53.3 ± 15.8 years, 85% women), mean 25OHD 24.8 ± 2.8 ng/mL; and 210 outpatients in G2 (56.7 ± 16.0 years, 83% women), mean 25OHD was 36.8 ± 4.8 ng/mL. G1 had the higher number of comorbidities, including altered glycemia, dyslipidemia, hypothyroidism, urinary tract diseases, arthropathy, secondary hyperparathyroidism, anemia, and neurological and psychiatric disorders. Osteoporosis and hypothyroidism were more prevalent in G2. After binary logistic regression, the variables age (OR 0.988, CI 0.97-1.00, p = 0.048), osteoporosis (OR 0.54, CI 0.36-0.80, p = 0.003), dyslipidemia (OR 1.61, CI 1.10-2.39, p = 0.015), arthropathy (OR 2.60, CI 1.40-5.10, p = 0.003), anemia (OR 15.41, CI 3.09-280.08, p = 0.008), and neurological and psychiatric diseases (OR 3.78, CI 1.98-7.88, p = 0.001) maintained significance.
Patients with serum 25OHD ≥ 20 and < 30 ng/mL had higher prevalence of comorbidities compared to ≥ 30 ng/mL.
本研究评估了在进行 25OHD 测量的 1 年内,25OHD 两个正常范围值(20 和 <30ng/mL)之间的门诊患者共病数量。
这是一项在 1 年内进行 25OHD 测量的横断面研究,排除了 25OHD <20 和 >50ng/mL、临床研究参与者以及患有肝病和慢性肾衰竭的患者。将患者分为两组:组 1(G1),25OHD ≥20 和 <30ng/mL;组 2(G2),250HD ≥30 和 ≤50ng/mL。回顾了患者的人口统计学、实验室和共病数据的病历。
从 529 名门诊患者中,319 名患者在 G1(53.3±15.8 岁,85%女性),平均 25OHD 为 24.8±2.8ng/mL;210 名患者在 G2(56.7±16.0 岁,83%女性),平均 25OHD 为 36.8±4.8ng/mL。G1 的共病数量更高,包括血糖异常、血脂异常、甲状腺功能减退症、尿路感染、关节病、继发性甲状旁腺功能亢进症、贫血、神经和精神疾病。G2 中骨质疏松症和甲状腺功能减退症更为常见。二元逻辑回归后,变量年龄(OR 0.988,CI 0.97-1.00,p=0.048)、骨质疏松症(OR 0.54,CI 0.36-0.80,p=0.003)、血脂异常(OR 1.61,CI 1.10-2.39,p=0.015)、关节病(OR 2.60,CI 1.40-5.10,p=0.003)、贫血(OR 15.41,CI 3.09-280.08,p=0.008)和神经和精神疾病(OR 3.78,CI 1.98-7.88,p=0.001)仍然具有统计学意义。
与 25OHD ≥30ng/mL 相比,血清 25OHD 为 20 和 <30ng/mL 的患者共病患病率更高。