Pioglitazone increases serum magnesium levels in glucose-intolerant subjects.: A randomized, controlled trial

被引:16
作者
Guerrero-Romero, F
Rodríguez-Morán, M
机构
[1] Mexican Social Secur Inst, Med Res Unit Clin Epidemiol, Durango, Mexico
[2] Res Grp Diabet & Chron Illnesses, Durango, Mexico
关键词
pioglitazone; magnesium; thiazolidinediones; impaired glucose tolerance;
D O I
10.1055/s-2003-39236
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although thiazolidinediones and magnesium supplementation improves insulin action and increases HDL-cholesterol, the potential link between serum magnesium and thiazolidinediones has received little attention. Focusing on the increase of serum magnesium, 63 eligible subjects were enrolled and randomly allocated to receive either 30 mg Pioglitazone once daily (Group A) or lifestyle intervention (Group B) during 12 weeks. Subjects were eligible if they were glucose-intolerant, and excluded if they had high blood pressure, diabetes or abnormal liver function tests. The personnel assessing outcomes were blinded to group assignment. Of the 63 eligible subjects, 3 dropped out (one in group A, and two in Group B) because they moved out of the city. So, 30 subjects in each group, who satisfactorily completed the follow-up, were included in the analysis of data. There were no serious adverse events or side effects due to Pioglitazone or lifestyle intervention. At baseline, the groups did not differ significantly in serum magnesium levels 1.73 +/- 0.17 versus 1.72 +/- 0.14 mg/dl, p = 0.80. Subjects who received Pioglitazone significantly increased their serum magnesium to 1.93 +/- 0.16 mg/dl whereas in the lifestyle intervention group the increase was 1.74 +/- 0.25 mg/dl, p < 0.0001. What this study showed was a significant increase in the serum magnesium levels of glucose-intolerant subjects who received 30 mg Pioglitazone once daily.
引用
收藏
页码:91 / 96
页数:6
相关论文
共 44 条
[1]  
[Anonymous], 1997, ARCH INTERN MED, V157, P2413, DOI [10.1001/archinte.1997.00440420033005, DOI 10.1001/ARCHINTE.1997.00440420033005]
[2]  
Belcher G, 2000, EXP CLIN ENDOCR DIAB, V108, pS267
[3]  
Buse JB, 2000, EXP CLIN ENDOCR DIAB, V108, pS250
[4]  
Corica Francesco, 1994, Magnesium Research, V7, P43
[5]   Clinical pharmacokinetics of pioglitazone [J].
Eckland, DA ;
Danhof, M .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2000, 108 :S234-S242
[6]   HYPOMAGNESEMIA IN TYPE-II DIABETES - EFFECT OF A 3-MONTH REPLACEMENT THERAPY [J].
EIBL, NL ;
KOPP, HP ;
NOWAK, HR ;
SCHNACK, CJ ;
HOPMEIER, PG ;
SCHERNTHANER, G .
DIABETES CARE, 1995, 18 (02) :188-192
[7]   Placebo-controlled trials and active-control trials in the evaluation of new treatments - Part 2: Practical issues and specific cases [J].
Ellenberg, SS ;
Temple, R .
ANNALS OF INTERNAL MEDICINE, 2000, 133 (06) :464-470
[8]   Prevention of Type II diabetes in subjects with impaired glucose tolerance:: the Diabetes Prevention Study (DPS) in Finland -: Study design and 1-year interim report on the feasibility of the lifestyle intervention programme [J].
Eriksson, J ;
Lindström, J ;
Valle, T ;
Aunola, S ;
Hämäläinen, H ;
Ilanne-Parikka, P ;
Keinänen-Kiukaanniemi, S ;
Laakso, M ;
Lauhkonen, M ;
Lehto, P ;
Lehtonen, A ;
Louheranta, A ;
Mannelin, M ;
Martikkala, V ;
Rastas, M ;
Sundvall, J ;
Turpeinen, A ;
Viljanen, T ;
Uusitupa, M ;
Tuomilehto, J .
DIABETOLOGIA, 1999, 42 (07) :793-801
[9]   No excess 12-year mortality in men with impaired glucose tolerance who participated in the Malmo Preventive Trial with diet and exercise [J].
Eriksson, KF ;
Lindgärde, F .
DIABETOLOGIA, 1998, 41 (09) :1010-1016
[10]  
*EXP COMM DIAGN CL, 1999, DIABETES CARE S1, V22, P55