The effects of zinc supplementation on clinical response and metabolic profiles in pregnant women at risk for intrauterine growth restriction: a randomized, double-blind, placebo-controlled trial
سال انتشار: 1398
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 386
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شناسه ملی سند علمی:
DTOGIMED03_181
تاریخ نمایه سازی: 26 بهمن 1398
چکیده مقاله:
Background and Aim : Background: Data on the effects of zinc supplementation on clinical response andmetabolic profiles in women at risk for intrauterine growth restriction (IUGR) are limited. Thisinvestigation was conducted to assess the effects of zinc supplementation on clinical response and metabolicstatus among pregnant women at risk for IUGR.Methods : Methods: This randomized, double-blind, placebo-controlled, clinical trial was conductedamong 52 women at risk for IUGR according to abnormal uterine artery Doppler waveform. Participantswere randomly assigned to take either 233 mg zinc gluconate (containing 30 mg zinc) supplements (n=26)or placebo (n=26) for 10 weeks from 17-27 weeks of gestation. Fasting blood samples were taken atbaseline and after the 10-week treatment to quantify related variables.Results : Results: After the 10-week intervention, taking zinc led to a significant reduction in serum highsensitivity C-reactive protein (hs-CRP) (β -1.17 mg/L; 95% CI, -1.77, -0.57; P<0.001) and plasmamalondialdehyde (MDA) levels (β -0.23 μmol/L; 95% CI, -0.45, -0.02; P=0.03); also a significant rise intotal antioxidant capacity (TAC) (β 59.22 mmol/L; 95% CI, 25.07, 93.36; P=0.001) was observed incomparison to placebo. In addition, zinc supplementation significantly reduced serum insulin (β -1.33μIU/mL; 95% CI, -2.00, -0.67; P<0.001) and insulin resistance (β -0.30; 95% CI, -0.44, -0.15; P<0.001),and significantly increased insulin sensitivity (β 0.008; 95% CI, 0.003, 0.01; P<0.001) compared with theplacebo.Conclusion : Conclusions: Zinc supplementation did not influence pulsatility index (PI) and othermetabolic parameters. Overall, zinc supplementation in pregnant women at risk for IUGR had beneficialeffects on TAC, MDA, hs-CRP and insulin metabolism, but did not affect PI and other metabolic profiles.
کلیدواژه ها:
نویسندگان
Elaheh Mesdaghinia
Department of Gynecology and Obstetrics, School of Medicine, Kashan University of Medical Sciences, Kashan, I.R. Iran
Fatemeh Naderi
Department of Gynecology and Obstetrics, School of Medicine, Kashan University of Medical Sciences, Kashan, I.R. Iran
Zatollah Asemi
Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences,Kashan, I.R. Iran