TY - JOUR
T1 - Clinical and Genetic Factors Associated with Thiazide-Induced Hyponatremia
AU - Huang, Chin Chou
AU - Chung, Chia Min
AU - Hung, Shuen Iu
AU - Pan, Wen Harn
AU - Leu, Hsin Bang
AU - Huang, Po Hsun
AU - Chiu, Chun Chih
AU - Lin, Liang Yu
AU - Lin, Chih Ching
AU - Yang, Chih Yu
AU - Li, Szu Yuan
AU - Chen, Yen Chia
AU - Wu, Tao Cheng
AU - Lin, Shing Jong
AU - Chen, Jaw Wen
N1 - Publisher Copyright:
© 2015 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Thiazide diuretics are associated with an increased risk of hyponatremia. The aim of this study was to investigate possible predictors of thiazide-induced hyponatremia. A total of 48 patients admitted to the ward or to the emergency department due to severe thiazide-induced hyponatremia (Na<125mmol/L) were enrolled in our study as the case group. Another 211 hypertensive patients with normal sodium levels after treatment with thiazide diuretics were selected as the control group. Twelve tag single nucleotide polymorphism markers were selected from the Potassium Channel, Inwardly Rectifying Subfamily J, Member 1 (KCNJ1) gene: rs1231254, rs2238009, rs1148058, rs675482, rs673614, rs12795437, rs2855800, rs2509585, rs3016774, rs881333, rs4529890, and rs7116606. Clinical and genetic parameters between patients with thiazide-induced hyponatremia and the control group were compared. Logistic regression was used to analyze data. The patients with thiazide-induced hyponatremia were older (P<0.001), predominantly female (P=0.008), had a lower mean body mass index (BMI) (P<0.001), and more commonly used angiotensin II receptor antagonist (P<0.001) and spironolactone (P=0.007) compared with the control groups. Analysis with multivariate logistic regression revealed that age (odds ratio [OR], 1.13; 95% confidence interval [CI], 1.08-1.19, P<0.001), female gender (OR, 4.49; 95% CI, 1.54-13.11, P=0.006), BMI (OR, 0.80; 95% CI, 0.69-0.93, P=0.003), and KCNJ1 rs2509585C/T or T/T polymorphisms (OR, 5.75; 95% CI, 1.25-26.45, P=0.03) were independent predictors for thiazide-induced hyponatremia. Older female patients with lower BMIs and KCNJ1 rs2509585C/T or T/T polymorphisms were more likely to develop thiazide-induced hyponatremia.
AB - Thiazide diuretics are associated with an increased risk of hyponatremia. The aim of this study was to investigate possible predictors of thiazide-induced hyponatremia. A total of 48 patients admitted to the ward or to the emergency department due to severe thiazide-induced hyponatremia (Na<125mmol/L) were enrolled in our study as the case group. Another 211 hypertensive patients with normal sodium levels after treatment with thiazide diuretics were selected as the control group. Twelve tag single nucleotide polymorphism markers were selected from the Potassium Channel, Inwardly Rectifying Subfamily J, Member 1 (KCNJ1) gene: rs1231254, rs2238009, rs1148058, rs675482, rs673614, rs12795437, rs2855800, rs2509585, rs3016774, rs881333, rs4529890, and rs7116606. Clinical and genetic parameters between patients with thiazide-induced hyponatremia and the control group were compared. Logistic regression was used to analyze data. The patients with thiazide-induced hyponatremia were older (P<0.001), predominantly female (P=0.008), had a lower mean body mass index (BMI) (P<0.001), and more commonly used angiotensin II receptor antagonist (P<0.001) and spironolactone (P=0.007) compared with the control groups. Analysis with multivariate logistic regression revealed that age (odds ratio [OR], 1.13; 95% confidence interval [CI], 1.08-1.19, P<0.001), female gender (OR, 4.49; 95% CI, 1.54-13.11, P=0.006), BMI (OR, 0.80; 95% CI, 0.69-0.93, P=0.003), and KCNJ1 rs2509585C/T or T/T polymorphisms (OR, 5.75; 95% CI, 1.25-26.45, P=0.03) were independent predictors for thiazide-induced hyponatremia. Older female patients with lower BMIs and KCNJ1 rs2509585C/T or T/T polymorphisms were more likely to develop thiazide-induced hyponatremia.
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U2 - 10.1097/MD.0000000000001422
DO - 10.1097/MD.0000000000001422
M3 - Article
C2 - 26313793
AN - SCOPUS:84944871289
SN - 0025-7974
VL - 94
SP - e1422
JO - Medicine (United States)
JF - Medicine (United States)
IS - 34
ER -