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    <title>JAMA Pediatrics: Lipids and Lipid Disorders Topic Collection</title>
    <link>http://archpedi.jamanetwork.com/</link>
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    <pubDate>Mon, 03 Jun 2013 00:00:00 GMT</pubDate>
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      <title>Flaxseed in Pediatric Hyperlipidemia A Placebo-Controlled, Blinded, Randomized Clinical Trial of Dietary Flaxseed Supplementation for Children and Adolescents With Hypercholesterolemia  Flaxseed in Pediatric Hyperlipidemia </title>
      <link>http://archpedi.jamanetwork.com/article.aspx?articleID=1692333</link>
      <pubDate>Mon, 03 Jun 2013 00:00:00 GMT</pubDate>
      <author>Wong H, Chahal N, Manlhiot C, et al. </author>
      <description>&lt;span class="paragraphSection"&gt;&lt;div class="boxTitle"&gt;Importance&lt;/div&gt;Nonpharmacological management of hypercholesterolemia in children is challenging with few available options.&lt;div class="boxTitle"&gt;Objectives&lt;/div&gt;To determine the safety and efficacy of dietary flaxseed supplementation in the management of hypercholesterolemia in children.&lt;div class="boxTitle"&gt;Design&lt;/div&gt;Four-week placebo-controlled, blinded, randomized clinical trial.&lt;div class="boxTitle"&gt;Setting&lt;/div&gt;Specialized dyslipidemia clinic at a tertiary pediatric care center.&lt;div class="boxTitle"&gt;Participants&lt;/div&gt;Thirty-two participants aged 8 to 18 years with low-density lipoprotein cholesterol from 135 mg/dL (3.5 mmol/L) to less than 193 mg/dL (5.0 mmol/L).&lt;div class="boxTitle"&gt;Intervention&lt;/div&gt;The intervention group ate 2 muffins and 1 slice of bread daily containing ground flaxseed (30 g flaxseed total). The control group ate muffins and bread substituted with whole-wheat flour.&lt;div class="boxTitle"&gt;Main Outcome and Measure&lt;/div&gt;Attributable change in fasting lipid profile.&lt;div class="boxTitle"&gt;Results&lt;/div&gt;Dietary flaxseed supplementation resulted in an attributable decrease of −7.35 mg/dL (–0.19 mmol/L) in high-density lipoprotein cholesterol (95% CI, −3.09 to −11.60 mg/dL[−0.08 to −0.30 mmol/L]; relative: −15%, 95% CI, −24% to −6%; P = .001), an increase of 29.23 mg/dL (+0.33 mmol/L) in triglycerides (95% CI, 4.43 to 53.14 mg/dL [+0.05 to +0.60 mmol/L]; relative: +26%, 95% CI, +4% to +48%; P = .02), and an increase of +4.88 g/d in dietary polyunsaturated fat intake (95% CI, +0.22 to +9.53; relative: +76%, 95% CI, +3% to +148%; P = .04). Flaxseed had no attributable effects on total cholesterol (−8.51 mg/dL [−0.22 mmol/L]; 95% CI, −21.66 to 4.25 mg/dL [−0.56 to +0.11 mmol/L]; relative: −4%, 95% CI, −10% to +2%; P = .20), low-density lipoprotein cholesterol (−6.96 mg/dL [−0.18 mmol/L]; 95% CI, −16.63 to 2.71 mg/dL [−0.43 to +0.07 mmol/L]; relative: −5%, 95% CI, −12% to +2%; P = .15), body mass index z score (+0.002; 95% CI, −0.147 to +0.150; relative: +0%, 95% CI, −12% to +12%; P = .30), or total caloric intake (+117 kcal; 95% CI, −243 to +479; relative: +8%, 95% CI, −17% to +33%; P = .52). An attributable change in total and low-density lipoprotein cholesterol failed to exclude a potential benefit of flaxseed supplementation based on a prespecified minimum clinically important reduction of 10%. No concerns were noted regarding safety.&lt;div class="boxTitle"&gt;Conclusions and Relevance&lt;/div&gt;The use of dietary flaxseed supplementation, while safe, was associated with adverse changes in the lipid profile of children with hypercholesterolemia, although a potential benefit of low-density lipoprotein cholesterol lowering could not be excluded. The use of flaxseed supplementation in children with hypercholesterolemia might not be a viable option for lipid management in this population.&lt;div class="boxTitle"&gt;Trial Registration&lt;/div&gt;clinicaltrials.gov Identifier: NCT01007344&lt;/span&gt;</description>
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      <prism:doi xmlns:prism="prism">10.1001/jamapediatrics.2013.1442</prism:doi>
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