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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Kong, L. C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Wuillemin, P. H.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bastard, J. P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sokolovska, N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Gougis, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Fellahi, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Darakhshan, F.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bonnefont-Rousselot, D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bittar, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Dore, J.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Zucker, Jean-Daniel</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Clement, K.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Rizkalla, S.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Insulin resistance and inflammation predict kinetic body weight changes in response to dietary weight loss and maintenance in overweight and obese subjects by using a Bayesian network approach</title>
        <secondary-title>American Journal of Clinical Nutrition</secondary-title>
      </titles>
      <pages>1385-1394</pages>
      <dates>
        <year>2013</year>
      </dates>
      <call-num>fdi:010061354</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>American Journal of Clinical Nutrition</full-title>
      </periodical>
      <isbn>0002-9165</isbn>
      <accession-num>ISI:000328002000004</accession-num>
      <number>6</number>
      <electronic-resource-num>10.3945/ajcn.113.058099</electronic-resource-num>
      <urls>
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          <url>https://www.documentation.ird.fr/hor/fdi:010061354</url>
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          <url>https://www.documentation.ird.fr/intranet/publi/2014/01/010061354.pdf</url>
        </pdf-urls>
      </urls>
      <volume>98</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background: The ability to identify obese subjects who will lose weight in response to energy restriction is an important strategy in obesity treatment. Objective: We aimed to identify obese subjects who would lose weight and maintain weight loss through 6 wk of energy restriction and 6 wk of weight maintenance. Design: Fifty obese or overweight subjects underwent a 6-wk energy-restricted, high-protein diet followed by another 6 wk of weight maintenance. Network modeling by using combined biological, gut microbiota, and environmental factors was performed to identify predictors of weight trajectories. Results: On the basis of body weight trajectories, 3 subject clusters were identified. Clusters A and B lost more weight during energy restriction. During the stabilization phase, cluster A continued to lose weight, whereas cluster B remained stable. Cluster C lost less and rapidly regained weight during the stabilization period. At baseline, cluster C had the highest plasma insulin, interleukin (IL)-6, adipose tissue inflammation (HAM56+ cells), and Lactobacillus/Leuconostoc/Pediococcus numbers in fecal samples. Weight regain after energy restriction correlated positively with insulin resistance (homeostasis model assessment of insulin resistance: r = 0.5, P = 0.0002) and inflammatory markers (IL-6; r = 0.43, P = 0.002) at baseline. The Bayesian network identified plasma insulin, IL-6, leukocyte number, and adipose tissue (HAM56) at baseline as predictors that were sufficient to characterize the 3 clusters. The prediction accuracy reached 75.5%. Conclusion: The resistance to weight loss and proneness to weight regain could be predicted by the combination of high plasma insulin and inflammatory markers before dietary intervention.</abstract>
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