<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">FNS</journal-id><journal-title-group><journal-title>Food and Nutrition Sciences</journal-title></journal-title-group><issn pub-type="epub">2157-944X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fns.2015.617163</article-id><article-id pub-id-type="publisher-id">FNS-62121</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Effect of Daily Consumption of &lt;i&gt; Lactobacillus reuteri &lt;/i&gt; CRL 1098 on Cholesterol Reduction in Hypercholesterolemic Subjects
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>gustina</surname><given-names>Malpeli</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mar&amp;iacute;a</surname><given-names>P&amp;iacute;a Taranto</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ricardo</surname><given-names>C. Cravero</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Marina</surname><given-names>Tavella</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Victoria</surname><given-names>Fasano</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dimas</surname><given-names>Vicentin</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Guillermina</surname><given-names>Ferrari</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Graciano</surname><given-names>Magrini</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Elvira</surname><given-names>H&amp;eacute;bert</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Graciela</surname><given-names>Font de Valdez</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ana</surname><given-names>M. Varea</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Julio</surname><given-names>M. Tavella</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Horacio</surname><given-names>F. Gonz&amp;aacute;lez</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>CERELA—Centro de Referencia para Lactobacilos (CONICET), Tucum&amp;amp;aacute;n, Argentina</addr-line></aff><aff id="aff1"><addr-line>IDIP—Instituto de Desarrollo e Investigaciones Pedi&amp;amp;aacute;tricas “Prof. Dr. Fernando E. Viteri” (Hospital de Ni&amp;amp;ntilde;os de La Plata, Ministerio de Salud/Comisi&amp;amp;oacute;n de Investigaciones Cient&amp;amp;iacute;ficas de la Pro-vincia de Buenos Aires), La Plata, Argentina</addr-line></aff><aff id="aff3"><addr-line>Sancor CUL, Departamento de Investigaci&amp;amp;oacute;n, Innovaci&amp;amp;oacute;n y Desarrollo, Sunchales, Argentina</addr-line></aff><pub-date pub-type="epub"><day>23</day><month>12</month><year>2015</year></pub-date><volume>06</volume><issue>17</issue><fpage>1583</fpage><lpage>1590</lpage><history><date date-type="received"><day>22</day>	<month>October</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>20</month>	<year>December</year>	</date><date date-type="accepted"><day>23</day>	<month>December</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The effect of daily consumption of a yogurt containing 
  <em>Lactobacillus reuteri </em>CRL 1098 on the lipid profile of hypercholesterolemic subjects was evaluated by performing a prospective, randomized, double-blind, cross-over placebo controlled clinical study. Participants consumed daily a yogurt containing
  <em> L. reuteri</em> CRL 1098 or a placebo for four weeks, separated by a wash-out period. Total cholesterol, triacylglycerol, high-density (HDL) and low-density (LDL) lipoprotein levels were assessed at the beginning and at the end of each period. We found a statistically significant reduction of total (
  –7.86 g/dl) and LDL (
  –7.02 g/dl) cholesterol in absolute changes (before-after) as well as a decreasing trend in the group receiving the yogurt containing
  <em> L. reuteri</em> with respect to the placebo group, without detecting changes in HDL-cholesterol and triacylglycerol levels. Our results suggest that low amounts of yogurt (125 g/day) and low doses of the CRL 1098 strain (10
  <sup>6</sup> CFU) are sufficient to reduce total and LDL-cholesterol levels in hypercholesterolemic subjects.
 
</p></abstract><kwd-group><kwd>&lt;i&gt; Lactobacillus reuteri &lt;/i&gt;</kwd><kwd> Hypercholesterolemia</kwd><kwd> Cardiovascular Risk</kwd><kwd> Probiotics</kwd><kwd> Functional Foods</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>High serum cholesterol levels are a risk factor for atherosclerosis and cardiovascular disease. In Western countries, cardiovascular disease is one of the leading causes of death, and is extending to Eastern countries to become the main mortality cause worldwide. In Argentina, 46% of deaths are due to cardiovascular disease, and approximately 30% - 40% of the population suffers some kind of hypercholesterolemia [<xref ref-type="bibr" rid="scirp.62121-ref1">1</xref>] -[<xref ref-type="bibr" rid="scirp.62121-ref4">4</xref>] .</p><p>In the last years, different nutraceutical and functional foods with hypocholesterolemic properties have been developed. In these cases, the effect would be related to the presence of several alternatives such as soy proteins, omega 3, plant sterols, polyphenols in green tea, wine and olive oil, and probiotic microorganisms as selected strains of lactic acid bacteria (LAB) [<xref ref-type="bibr" rid="scirp.62121-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.62121-ref6">6</xref>] .</p><p>The use of probiotic LAB strains capable of regulating hyperlipidemia in individuals with hypercholesterolemia is a natural alternative to help maintain healthy lipid levels without undesirable side effects. Research studies show that reduced cholesterol levels due to the use of certain LAB strains could be related to bile salt hydrolase (BSH) activity, present only in microorganisms. BSH<sup>+</sup> LAB strains are able to survive and colonize the small intestine, where the enterohepatic circulation takes place. Once in the intestine, these strains would act on the conjugated bile salts excreted during intake, releasing bile salts or free bile acids which cannot be reabsorbed from the gut and are excreted via the faeces. Under these circumstances, the concentration of bile acids, which should remain constant in the intestine, decreases. To maintain biliary homeostasis, the liver should synthesize more bile acids de novo from endogenous cholesterol. The altered metabolism of bile salts by increased BSH activity would also affect cholesterol metabolism, directly influencing its solubility and subsequent absorption at intestinal level [<xref ref-type="bibr" rid="scirp.62121-ref6">6</xref>] - [<xref ref-type="bibr" rid="scirp.62121-ref8">8</xref>] .</p><p>Different bifidobacteria and lactobacilli strains (Bifidobacterium lactis, B. longun, Lactobacillus plantarum, L. acidophilus, L. reuteri, L. fermentun) would be potentially effective for cholesterol reduction as evidenced through in vitro assays [<xref ref-type="bibr" rid="scirp.62121-ref7">7</xref>] . However, animal and human trials designed to demonstrate serum cholesterol reduction by LAB administration have reported controversial results [<xref ref-type="bibr" rid="scirp.62121-ref7">7</xref>] - [<xref ref-type="bibr" rid="scirp.62121-ref9">9</xref>] . In humans, some trials about the effect of LAB administration have shown decreased serum cholesterol levels [<xref ref-type="bibr" rid="scirp.62121-ref10">10</xref>] - [<xref ref-type="bibr" rid="scirp.62121-ref12">12</xref>] , whereas other studies have found no effect [<xref ref-type="bibr" rid="scirp.62121-ref13">13</xref>] - [<xref ref-type="bibr" rid="scirp.62121-ref15">15</xref>] .</p><p>The assessment of the effect of Lactobacillus (L.) reuteri CRL 1098 on lipid profile has had promising results. Taranto et al. [<xref ref-type="bibr" rid="scirp.62121-ref16">16</xref>] administered a fat-rich diet to mice for 7 days and then the animals were treated with a solution containing L. reuteri CRL 1098 (10<sup>4</sup> cells/day). In the intervention group, total cholesterol and triacylglycerol levels decreased by 38 and 40%, respectively, whereas the HDL/LDL-cholesterol ratio increased by 20%, without producing side effects.</p><p>Another report in mice [<xref ref-type="bibr" rid="scirp.62121-ref17">17</xref>] showed that L. reuteri CRL 1098 administration was effective in preventing hypercholesterolemia and further confirmed its permanence in the gut. However, there are no studies reporting the probiotic effect on hypercholesterolemic subjects thus far.</p><p>This study was undertaken to evaluate the effect of the daily consumption of L. reuteri CRL 1098-containing yogurt during four weeks on total, HDL-, LDL-cholesterol and triacylglycerol levels in hypercholesterolemic subjects.</p></sec><sec id="s2"><title>2. Material and Methods</title><sec id="s2_1"><title>2.1. Study Sample and Sample Size Estimation Electing a Template</title><p>Participants were recruited through announcements placed in public institutions from the city of La Plata, Buenos Aires, Argentina. Eligible participants were healthy men and women over the age of 18 years, with hypercholesterolemia (total cholesterol &gt; 200 mg/dl) confirmed with laboratory test at the beginning of the study, and not taking any hypocholesterolemic drug.</p><p>Inclusion and exclusion criteria of the study sample are summarized in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>Sample size was estimated to have 90% power and 95% confidence interval to detect differences of 20 mg/dl in cholesterol levels between the intervention and the placebo group at the end of the 4-week study period. Thus, the required sample size was 60 participants in each group (20% loss adjustment; 30 mg/dl standard deviation).</p></sec><sec id="s2_2"><title>2.2. Study Design</title><p>We performed a prospective, randomized, double-blind, cross-over placebo controlled clinical study. Random</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Inclusion and exclusion criteria of the study sample</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Inclusion criteria</th><th align="center" valign="middle" >Exclusion criteria</th></tr></thead><tr><td align="center" valign="middle" >Older than 18 years of age Total cholesterol levels higher than 200 mg/dl</td><td align="center" valign="middle" >Use of statins or other cholesterol-lowering drugs within the previous 6 months. Use of cholesterol lowering supplements within the previous 3 months. Use of systemic antibodies, corticosteroids, androgens or phenitoin. Lactose intolerance or milk allergy. History of inflammatory bowel disease or pancreatitis. Gastrointestinal, renal, hepatic, lung or bile disease. Hypo/hyperthyroidism. Menopause. Family history of hypercholesterolemia. Chronic use of probiotics (&gt;2 doses/week), fiber-based laxatives (&gt;2 doses/week) or stimulant laxatives. Diabetes mellitus or cancer. Alcohol abuse (&gt;40 g/day). Pregnancy or breastfeeding.</td></tr></tbody></table></table-wrap><p>allocation of study participants to the intervention or placebo group was performed with EPIDAT 3.1 (1:1 allocation ratio).</p><p>The study was organized in four visits formed by three consecutive stages that lasted four weeks each. Initially, participants were assigned to consume one yogurt daily (125 g) with (intervention group) and without (placebo group) L. reuteri CRL 1098 during four weeks.</p><p>The lipid profile was determined on the first visit; participants were given information and advice on healthy diet and were asked to maintain their habitual lifestyle and to eat the yogurt any time of the day. On the second visit, the lipid profile was determined again and participants began the wash-out period during which no product was consumed. On the third visit, the lipid profile test was repeated and participants of both groups (placebo and intervention) were crossed over for four weeks, i.e., those who had consumed the 125-g placebo yogurt started to eat the intervention yogurt (with L. reuteri CRL 1098), and participants who had received the probiotic-con- taining yogurt now received the placebo yogurt.</p><p>At the end of this stage, on the fourth visit, participants performed the final laboratory test.</p><p>On visits 1 and 4, anthropometric parameters (weight, height, waist and abdominal circumference), dietary changes, physical activity practice as well as tobacco and alcohol consumption were recorded together with any side effect.</p></sec><sec id="s2_3"><title>2.3. Characteristics of the Intervention Yogurt</title><p>The strain used in this study (L. reuteri CRL 1098) was obtained from the CERELA culture collection (San Miguel de Tucum&#225;n, Argentina). The microorganism was cultured in MRS agar at 37˚C for 16 h. Cells were collected by centrifugation at 6000/g during 10 min, washed three times with sterile saline solution, suspended in 10% sterile skimmed milk powder and the biomass produced was finally freeze-dried at Biochemical S.A. (Libertad, Buenos Aires, Argentina). One gram of lyophilized product contained 10<sup>10</sup> CFU; the inoculum was used industrially to produce the intervention yogurt, which contained the same amount of product plus 10<sup>6</sup> CFU of L. reuteri CRL 1098 per gram of yogurt.</p></sec><sec id="s2_4"><title>2.4. Control, Follow-Up and Yogurt Preservation</title><p>Both yogurts were produced and prepared by SanCor C.U.L. (C&#243;rdoba, Argentina) and filled into 125 g plastic pots.</p><p>Addition of the probiotic strain CRL 1098 did not modify the fermentation curve, flavor, texture and consistency of the yogurt, which preserved the same organoleptic properties as the placebo yogurt.</p><p>Postacidification was not observed in either the control or the intervention yogurt.</p><p>L. reuteri CRL 1098 colony counts during the life span of the product were above the minimum amount established to perform clinical trials (&gt;10E+06 CFU).</p></sec><sec id="s2_5"><title>2.5. Data Collection</title><p>Weight, height and waist circumference were taken on visits 1 and 4. Body weight was measured barefoot and in light clothing with a Tanita scale (0.1 g precision, Tanita Corporation of America, Inc. Illinois, USA). Height was measured with a SECA stadiometer (0.5 cm precision, SECA, UK) and waist circumference with an inextensible measuring tape (1 mm precision).</p><p>Blood pressure was taken on visits 1 and 4 with an OMROM digital blood pressure monitor.</p><p>Physical activity was assessed during visit 1 using the IPAQ questionnaire [<xref ref-type="bibr" rid="scirp.62121-ref18">18</xref>] . The level of physical activity was categorised according to the IPAQ’s scoring protocol in multiples of the resting metabolic rate (METS) as low, moderate and intense. Dietary habits were determined with the 14-item Mediterranean Diet Assessment Tool [<xref ref-type="bibr" rid="scirp.62121-ref19">19</xref>] . Tobacco use was measured with the STEPwise approach to chronic disease risk factor surveillance recommended by the World Health Organization [<xref ref-type="bibr" rid="scirp.62121-ref20">20</xref>] .</p><p>Serum cholesterol (total, LDL and HDL) and triacylglycerol levels were determined by enzymatic reactive kits during each of the four visits (Sigma Chemical Co., St. Louis, MO).</p></sec><sec id="s2_6"><title>2.6. Data Analysis</title><p>Data were analysed using SPSS version 19 for Windows. Continuous variables are presented as means &#177; standard deviation or medians (interquartile range), and qualitative variables are presented as percentages. All variables were examined for normality using the Kolmog&#243;rov-Smirnov test. Excepting triacylglycerol, all variables were normal. Data comparison at the beginning of the study was made with Student’s t-test for quantitative variables and Chi-square test for categorical variables. Comparison of initial mean cholesterol levels between groups was performed with Student’s t-test and Mann-Whitney Wilcoxon test for normal and non- normal (triacylglycerol) variables, respectively. Before-after differences in cholesterol levels within groups were studied with paired Student’s t-test for normal distribution variables and Wilcoxon signed rank test for non- normal distribution variables.</p><p>Differences in cholesterol levels between groups were compared with two-factor repeated measures analysis of variance (ANOVA) for normal variables and Friedman Test for triaglylglycerol. In all cases, P values &lt; 0.05 were considered statistically significant.</p></sec><sec id="s2_7"><title>2.7. Ethical Considerations</title><p>Current legal provisions implemented by the Joint Health Research Committee, Ministry of Health of the Province of Buenos Aires, Argentina, were considered. The study protocol was reviewed and approved by said Committee and by the corresponding Institutional Ethics Committee. Participants signed informed consent forms, received oral and written information about the study prior to participation, and could voluntarily abandon the project at any moment. The study was conducted in accordance with the Helsinki Declaration and the current Good Clinical Practice principles.</p></sec></sec><sec id="s3"><title>3. Results</title><p>A total of 105 healthy adult subjects voluntarily agreed to participate in the study. After excluding those who did not meet the inclusion criteria (n = 35), 70 subjects were randomly assigned to the study groups. The general characteristics of the placebo and intervention groups at the beginning of the study are presented in <xref ref-type="table" rid="table2">Table 2</xref>. Age, BMI and blood pressure values were similar in both groups. Half of the patients had a sedentary lifestyle, as determined by IPAQ, and about a quarter of them were smokers. Only waist circumference values were higher in the intervention group (P = 0.043).</p><p><xref ref-type="table" rid="table3">Table 3</xref> shows that total and LDL-cholesterol levels decreased significantly (P = 0.017 and P = 0.019, respectively) in participants that consumed the yogurt containing L. reuteri CRL 1098, whereas HDL-cholesterol and triaclyglycerol levels did not change significantly. On the other hand, no changes could be observed in the placebo group in any of the lipid profile parameters studied.</p><p>Although changes in the lipid profile of participants before and after consuming the placebo and the intervention yogurts were not statistically significant, a trend towards lower total cholesterol (P = 0.076) and LDL-cho- lesterol (P = 0.08) levels was found in the intervention group (<xref ref-type="table" rid="table4">Table 4</xref>).</p><p>LDL-cholesterol decreased (3.96%) in the intervention as compared with the control group, in which case an increase could be detected (3.24%), showing a significant trend (P = 0.059).</p><p>Adherence to the Mediterranean diet was similar in both groups; 33.3% and 29.6% of participants in the</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Clinical characteristics of participants in the placebo and intervention groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Placebo (n = 37)</th><th align="center" valign="middle" >Intervention (n = 33)</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Age (years) (mean &#177; SD)</td><td align="center" valign="middle" >42.8 &#177; 11.6</td><td align="center" valign="middle" >47.6 &#177; 12.4</td><td align="center" valign="middle" >0.101</td></tr><tr><td align="center" valign="middle" >BMI (kg/m<sup>2</sup>) (mean &#177; SD)</td><td align="center" valign="middle" >26.16 &#177; 4.09</td><td align="center" valign="middle" >27.58 &#177; 5.48</td><td align="center" valign="middle" >0.245</td></tr><tr><td align="center" valign="middle" >Waist circumference (cm) (mean &#177; SD)</td><td align="center" valign="middle" >87 &#177; 13</td><td align="center" valign="middle" >94 &#177; 13</td><td align="center" valign="middle" >0.043</td></tr><tr><td align="center" valign="middle" >Systolic blood pressure (mmHg) (mean &#177; SD)</td><td align="center" valign="middle" >128 &#177; 16</td><td align="center" valign="middle" >127 &#177; 18</td><td align="center" valign="middle" >0.886</td></tr><tr><td align="center" valign="middle" >Diastolic blood pressure (mmHg) (mean &#177; SD)</td><td align="center" valign="middle" >74 &#177; 11</td><td align="center" valign="middle" >72 &#177; 11</td><td align="center" valign="middle" >0.429</td></tr><tr><td align="center" valign="middle" >Sedentary lifestyle (%)</td><td align="center" valign="middle" >49</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >0.91</td></tr><tr><td align="center" valign="middle" >Smoking (%)</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >0.94</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Changes in total, HDL-, LDL-cholesterol and triacylglycerol levels in the placebo and intervention groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Placebo Mean (SD) or Median (IQR)</th><th align="center" valign="middle" >P</th><th align="center" valign="middle" >Intervention Mean (SD) or Median (IQR)</th><th align="center" valign="middle" >P</th></tr></thead><tr><td align="center" valign="middle" >Cholesterol AbsΔ</td><td align="center" valign="middle" >−3.39 (24.55)</td><td align="center" valign="middle" >0.302<sup>a</sup></td><td align="center" valign="middle" >−7.86 (25.46)</td><td align="center" valign="middle" >0.017<sup>a</sup></td></tr><tr><td align="center" valign="middle" >HDL-cholesterol AbsΔ</td><td align="center" valign="middle" >−17.02 (7.62)</td><td align="center" valign="middle" >0.097<sup>a</sup></td><td align="center" valign="middle" >0.35 (9.83)</td><td align="center" valign="middle" >0.779<sup>a</sup></td></tr><tr><td align="center" valign="middle" >LDL-cholesterol AbsΔ</td><td align="center" valign="middle" >0.95 (24.68)</td><td align="center" valign="middle" >0.775<sup>a</sup></td><td align="center" valign="middle" >−7.02 (23.03)</td><td align="center" valign="middle" >0.019<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Triacylglycerol AbsΔ</td><td align="center" valign="middle" >−3.5 (−28.75. 17.75)</td><td align="center" valign="middle" >0.337<sup>b</sup></td><td align="center" valign="middle" >1 (−29. 18)</td><td align="center" valign="middle" >0.619<sup>b</sup></td></tr></tbody></table></table-wrap><p><sup>a</sup>Paired Student’s t-test. <sup>b</sup>Wilcoxon signed rank test.</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Basal data and absolute changes in total, HDL-, LDL-cholesterol and triacylglycerol levels in both study groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Placebo Mean (SD) or Median (IQR)</th><th align="center" valign="middle" >Intervention Mean (SD) or Median (IQR)</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Total cholesterol</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Baseline</td><td align="center" valign="middle" >224.34 (30.72)</td><td align="center" valign="middle" >230.45 (28.76)</td><td align="center" valign="middle" >0.251<sup>a </sup></td></tr><tr><td align="center" valign="middle" >AbsΔ<sup>*</sup></td><td align="center" valign="middle" >−3.39 (24.55)</td><td align="center" valign="middle" >−7.86 (25.46)</td><td align="center" valign="middle" >0.076<sup>b </sup></td></tr><tr><td align="center" valign="middle" >HDL-cholesterol</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Baseline</td><td align="center" valign="middle" >50.32 (12.51)</td><td align="center" valign="middle" >48.23 (11.96)</td><td align="center" valign="middle" >0.340<sup>a </sup></td></tr><tr><td align="center" valign="middle" >AbsΔ<sup>*</sup></td><td align="center" valign="middle" >−17.02 (7.62)</td><td align="center" valign="middle" >0.35 (9.83)</td><td align="center" valign="middle" >0.828<sup>b </sup></td></tr><tr><td align="center" valign="middle" >LDL-cholesterol</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Baseline</td><td align="center" valign="middle" >148.59 (31.60)</td><td align="center" valign="middle" >156.97 (28.68)</td><td align="center" valign="middle" >0.124<sup>a </sup></td></tr><tr><td align="center" valign="middle" >AbsΔ<sup>*</sup></td><td align="center" valign="middle" >0.95 (24.68)</td><td align="center" valign="middle" >−7.02 (23.03)</td><td align="center" valign="middle" >0.088<sup>b </sup></td></tr><tr><td align="center" valign="middle" >Triacylglycerol</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Baseline</td><td align="center" valign="middle" >106 (75.5. 158.5)</td><td align="center" valign="middle" >114.5 (72.5. 150)</td><td align="center" valign="middle" >0.957<sup>c </sup></td></tr><tr><td align="center" valign="middle" >AbsΔ<sup>*</sup></td><td align="center" valign="middle" >−3.5 (−28.75. 17.75)</td><td align="center" valign="middle" >1 (−29. 18)</td><td align="center" valign="middle" >0.680<sup>d </sup></td></tr></tbody></table></table-wrap><p><sup>*</sup>AbsΔ = after-before. <sup>a</sup>Student’s t-Test. <sup>b</sup>Two-factor repeated measures analysis of variance. <sup>c</sup>Mann-Whitney Wilcoxon Test. <sup>d</sup>Friedman Test.</p><p>placebo and intervention groups had scores ≥ 7 (P = 0.764). During follow-up, no significant changes could be assessed in either group. Smoking and the frequency and intensity of the practice of physical activity remained the same throughout the study period.</p></sec><sec id="s4"><title>4. Discussion</title><p>In this work, we demonstrate the effect of L. reuteri CRL 1098 on hypercholesterolemic subjects through clinical trials. Our results show a trend towards lower total and LDL cholesterol levels with the yogurt containing L. reuteri CRL 1098. Absolute changes (before-after) with the yogurt containing the probiotic were significant. The decrease in total and LDL-cholesterol was statistically significant (−7.86 and −7.02 g/dl, respectively), whereas HDL-cholesterol and triacylglycerol levels did not change. In the placebo group, the lipid profile did not change significantly.</p><p>Several clinical trials tended to demonstrate the effect of probiotic formulations on the lipid profile, obtaining different and controversial results. Most works included microbial BSH+ strains [<xref ref-type="bibr" rid="scirp.62121-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.62121-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.62121-ref15">15</xref>] . Administration of 200-ml fermented milk with one strain of Enterococcus faecium and two strains of Streptococcus thermophilus to middle-aged Danish men during 6 weeks reduced LDL-cholesterol by 10% compared with a placebo yogurt [<xref ref-type="bibr" rid="scirp.62121-ref21">21</xref>] . Two other reports on the administration of milk fermented with the same strains but for a longer period (8 weeks) also showed favourable changes in LDL-cholesterol (adjusted by body weight) [<xref ref-type="bibr" rid="scirp.62121-ref22">22</xref>] and total cholesterol [<xref ref-type="bibr" rid="scirp.62121-ref23">23</xref>] levels compared with the consumption of a placebo. However, when the same strains (E. faecium and S. thermophilus) were tested in an English population, lower serum cholesterol levels could not be detected [<xref ref-type="bibr" rid="scirp.62121-ref24">24</xref>] , probably due to different dietary habits and intestinal microbiota in the study samples. The effect of a milk product fermented with fructooligosaccharides (FOS) and L. acidophilus LA1 on the lipid profile was also tested [<xref ref-type="bibr" rid="scirp.62121-ref25">25</xref>] . Although the authors reported the reduction of total (4.4%; P &lt; 0.001) and LDL-cholesterol (5.4%; P &lt; 0.005), new tests would be necessary to verify whether the lactobacillus or FOS caused such reduction [<xref ref-type="bibr" rid="scirp.62121-ref25">25</xref>] . In another study using the same strain but without FOS, no changes in the lipid profile of participants with normal to borderline high serum cholesterol levels were observed [<xref ref-type="bibr" rid="scirp.62121-ref13">13</xref>] . On the other hand, Anderson &amp; Gilliland [<xref ref-type="bibr" rid="scirp.62121-ref12">12</xref>] found that administration of milk fermented with L. acidophilus LA1 caused a 3% reduction in cholesterol levels.</p><p>Administration of tablets with L. acidophilus ATCC 4962 and L. bulgaricus ATCC 33409 did not modify serum lipoprotein levels compared with the placebo [<xref ref-type="bibr" rid="scirp.62121-ref26">26</xref>] .</p><p>Milk fermented with Bifidobacterium longum BL1 decreased total cholesterol only in volunteering subjects with initial cholesterol values &gt;240 &#181;g/dl, showing the potential efficacy of this strain for the treatment of blood lipids [<xref ref-type="bibr" rid="scirp.62121-ref11">11</xref>] . Another report showed that the association of L. acidophilus and B. lactis strains reduced cholesterol levels in hypercholesterolemic subjects compared with a standard placebo yogurt [<xref ref-type="bibr" rid="scirp.62121-ref10">10</xref>] . However, no differences in the lipid profile of women were observed after administration of a yogurt with the same strains included in a conventional yogurt [<xref ref-type="bibr" rid="scirp.62121-ref27">27</xref>] .</p><p>Jones et al. demonstrated that microencapsulated L. reuteri NCIMB 30242 given in yogurt for six weeks [<xref ref-type="bibr" rid="scirp.62121-ref28">28</xref>] and given as capsules for nine weeks [<xref ref-type="bibr" rid="scirp.62121-ref29">29</xref>] significantly lowered total and LDL-cholesterol levels.</p><p>In agreement with the results reported herein, a recent meta-analysis [<xref ref-type="bibr" rid="scirp.62121-ref30">30</xref>] including randomised controlled trials that evaluated the effects of probiotic consumption on blood lipids in 485 participants concluded that probiotics were useful to lower total and LDL-cholesterol levels, but could not modify HDL-cholesterol and triacylglycerol levels.</p><p>Our results are positive, since changes in total and LDL-cholesterol could be observed with low amounts of the yogurt (one pot with 125 g/day) and low concentrations of the strain L. reuteri CRL 1098 (10<sup>6</sup> CFU). The effective dose of L. reuteri CRL 1098 is the lowest reported in the literature for LAB probiotics able to decrease serum lipid without undesirable side effects. Most published works show similar results using higher volumes of the product, in some cases several daily doses, and/or consumption of larger amounts of the probiotic microorganism. Further, L. reuteri CRL1098 can be used as adjunct culture for developing fresh functional foods without requiring strategies to ensure their viability, such as microencapsulation, because this strain is highly resistant to gastrointestinal conditions and adverse technological processes.</p></sec><sec id="s5"><title>5. Conclusion</title><p>The results obtained in the present study demonstrate that consumption of a 125-g yogurt containing 10<sup>6</sup> CFU L. reuteri CRL 1098 reduced total cholesterol levels by 7.8% and LDL-cholesterol levels by 7%, suggesting the clinical importance of such intake. These results are promising, since a review on the primary prevention of myocardial infarction showed that 1% cholesterol reduction could in turn produce a 6% to 10% reduction in the risk for heart disease [<xref ref-type="bibr" rid="scirp.62121-ref31">31</xref>] .</p></sec><sec id="s6"><title>Acknowledgements</title><p>This study was funded by FONARSEC (Fondo Argentino Sectorial), Ministerio de Ciencia, Tecnolog&#237;a e Innovaci&#243;n Productiva (id:SGP:02), Argentina. We thank Natalia Alvarez for blood extractions, Andrea Touza for product handling and administration, Ver&#243;nica Molina, Marta Medici, Mariano Obregozo, Mar&#237;a Jos&#233; Fornaguera and Lourdez Cruz Pintos for technical assistance with the probiotic strain, and Adriana Di Maggio for correcting the manuscript.</p></sec><sec id="s7"><title>Cite this paper</title><p>AgustinaMalpeli,Mar&#237;a P&#237;aTaranto,Ricardo C.Cravero,MarinaTavella,VictoriaFasano,DimasVicentin,GuillerminaFerrari,GracianoMagrini,ElviraH&#233;bert,Graciela Font deValdez,Ana M.Varea,Julio M.Tavella,Horacio F.Gonz&#225;lez, (2015) Effect of Daily Consumption of Lactobacillus reuteri CRL 1098 on Cholesterol Reduction in Hypercholesterolemic Subjects. 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