Probiotic administration in early life, atopy, and asthma: a meta-analysis of clinical trials
Probiotics may reduce the risk of atopy and asthma in children. However, results from clinical trials have been conflicting, and several of them may have been underpowered. We performed a meta-analysis of randomized, placebo-controlled trials to assess the effects of probiotic supplementation on ato...
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Veröffentlicht in: | Pediatrics (Evanston) 2013-09, Vol.132 (3), p.e666-e676 |
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description | Probiotics may reduce the risk of atopy and asthma in children. However, results from clinical trials have been conflicting, and several of them may have been underpowered. We performed a meta-analysis of randomized, placebo-controlled trials to assess the effects of probiotic supplementation on atopic sensitization and asthma/wheeze prevention in children.
Random-effects models were used to calculate pooled risk estimates. Meta-regression was conducted to examine the effect of potential factors on probiotics efficacy.
Probiotics were effective in reducing total immunoglobulin E (IgE) (mean reduction: -7.59 U/mL [95% confidence interval (CI): -14.96 to -0.22]; P = .044). Meta-regression showed that the reduction in IgE was more pronounced with longer follow-up. Probiotics significantly reduced the risk of atopic sensitization when administered prenatally (relative risk: 0.88 [95% CI: 0.78 to 0.99]; P = .035 for positive result on the skin prick test and/or elevated specific IgE to common allergens) and postnatally (relative risk: 0.86 [95% CI: 0.75 to 0.98]; P = .027 for positive result on skin prick test). Administration of Lactobacillus acidophilus, compared with other strains, was associated with an increased risk of atopic sensitization (P = .002). Probiotics did not significantly reduce asthma/wheeze (relative risk: 0.96 [95% CI: 0.85 to 1.07]).
Prenatal and/or early-life probiotic administration reduces the risk of atopic sensitization and decreases the total IgE level in children but may not reduce the risk of asthma/wheeze. Follow-up duration and strain significantly modified these effects. Future trials for asthma prevention should carefully select probiotic strain and consider longer follow-up. |
doi_str_mv | 10.1542/peds.2013-0246 |
format | Article |
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Random-effects models were used to calculate pooled risk estimates. Meta-regression was conducted to examine the effect of potential factors on probiotics efficacy.
Probiotics were effective in reducing total immunoglobulin E (IgE) (mean reduction: -7.59 U/mL [95% confidence interval (CI): -14.96 to -0.22]; P = .044). Meta-regression showed that the reduction in IgE was more pronounced with longer follow-up. Probiotics significantly reduced the risk of atopic sensitization when administered prenatally (relative risk: 0.88 [95% CI: 0.78 to 0.99]; P = .035 for positive result on the skin prick test and/or elevated specific IgE to common allergens) and postnatally (relative risk: 0.86 [95% CI: 0.75 to 0.98]; P = .027 for positive result on skin prick test). Administration of Lactobacillus acidophilus, compared with other strains, was associated with an increased risk of atopic sensitization (P = .002). Probiotics did not significantly reduce asthma/wheeze (relative risk: 0.96 [95% CI: 0.85 to 1.07]).
Prenatal and/or early-life probiotic administration reduces the risk of atopic sensitization and decreases the total IgE level in children but may not reduce the risk of asthma/wheeze. Follow-up duration and strain significantly modified these effects. Future trials for asthma prevention should carefully select probiotic strain and consider longer follow-up.</description><identifier>ISSN: 0031-4005</identifier><identifier>EISSN: 1098-4275</identifier><identifier>DOI: 10.1542/peds.2013-0246</identifier><identifier>PMID: 23958764</identifier><identifier>CODEN: PEDIAU</identifier><language>eng</language><publisher>United States: American Academy of Pediatrics</publisher><subject>Adolescent ; Asthma ; Asthma - immunology ; Asthma - prevention & control ; Asthma in children ; Care and treatment ; Child ; Child, Preschool ; Childhood asthma ; Children & youth ; Clinical trials ; Dermatitis, Atopic - immunology ; Dermatitis, Atopic - prevention & control ; Dosage and administration ; Double-Blind Method ; Female ; Follow-Up Studies ; Humans ; Immunoglobulin E - blood ; Immunoglobulins ; Infant ; Infant, Newborn ; Lactobacillus acidophilus ; Male ; Pediatrics ; Pregnancy ; Prevention ; Probiotics ; Probiotics - administration & dosage ; Randomized Controlled Trials as Topic ; Regression analysis ; Respiratory Hypersensitivity - immunology ; Respiratory Hypersensitivity - prevention & control ; Risk ; Risk assessment ; Safety and security measures ; Treatment Outcome</subject><ispartof>Pediatrics (Evanston), 2013-09, Vol.132 (3), p.e666-e676</ispartof><rights>Copyright American Academy of Pediatrics Sep 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-dd5bd9424114bedca079898dabc3d6683b8c591a93da3cf181f7cad24f0b9403</citedby><cites>FETCH-LOGICAL-c460t-dd5bd9424114bedca079898dabc3d6683b8c591a93da3cf181f7cad24f0b9403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23958764$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Elazab, Nancy</creatorcontrib><creatorcontrib>Mendy, Angelico</creatorcontrib><creatorcontrib>Gasana, Janvier</creatorcontrib><creatorcontrib>Vieira, Edgar R</creatorcontrib><creatorcontrib>Quizon, Annabelle</creatorcontrib><creatorcontrib>Forno, Erick</creatorcontrib><title>Probiotic administration in early life, atopy, and asthma: a meta-analysis of clinical trials</title><title>Pediatrics (Evanston)</title><addtitle>Pediatrics</addtitle><description>Probiotics may reduce the risk of atopy and asthma in children. However, results from clinical trials have been conflicting, and several of them may have been underpowered. We performed a meta-analysis of randomized, placebo-controlled trials to assess the effects of probiotic supplementation on atopic sensitization and asthma/wheeze prevention in children.
Random-effects models were used to calculate pooled risk estimates. Meta-regression was conducted to examine the effect of potential factors on probiotics efficacy.
Probiotics were effective in reducing total immunoglobulin E (IgE) (mean reduction: -7.59 U/mL [95% confidence interval (CI): -14.96 to -0.22]; P = .044). Meta-regression showed that the reduction in IgE was more pronounced with longer follow-up. Probiotics significantly reduced the risk of atopic sensitization when administered prenatally (relative risk: 0.88 [95% CI: 0.78 to 0.99]; P = .035 for positive result on the skin prick test and/or elevated specific IgE to common allergens) and postnatally (relative risk: 0.86 [95% CI: 0.75 to 0.98]; P = .027 for positive result on skin prick test). Administration of Lactobacillus acidophilus, compared with other strains, was associated with an increased risk of atopic sensitization (P = .002). Probiotics did not significantly reduce asthma/wheeze (relative risk: 0.96 [95% CI: 0.85 to 1.07]).
Prenatal and/or early-life probiotic administration reduces the risk of atopic sensitization and decreases the total IgE level in children but may not reduce the risk of asthma/wheeze. Follow-up duration and strain significantly modified these effects. Future trials for asthma prevention should carefully select probiotic strain and consider longer follow-up.</description><subject>Adolescent</subject><subject>Asthma</subject><subject>Asthma - immunology</subject><subject>Asthma - prevention & control</subject><subject>Asthma in children</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Childhood asthma</subject><subject>Children & youth</subject><subject>Clinical trials</subject><subject>Dermatitis, Atopic - immunology</subject><subject>Dermatitis, Atopic - prevention & control</subject><subject>Dosage and administration</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunoglobulin E - blood</subject><subject>Immunoglobulins</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Lactobacillus acidophilus</subject><subject>Male</subject><subject>Pediatrics</subject><subject>Pregnancy</subject><subject>Prevention</subject><subject>Probiotics</subject><subject>Probiotics - administration & dosage</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Regression analysis</subject><subject>Respiratory Hypersensitivity - immunology</subject><subject>Respiratory Hypersensitivity - prevention & control</subject><subject>Risk</subject><subject>Risk assessment</subject><subject>Safety and security measures</subject><subject>Treatment Outcome</subject><issn>0031-4005</issn><issn>1098-4275</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0T1vFDEQBmALgcgRaCmRJRoK9hh_7K5NF534kiKFIi2yZm1vcORdH7ZPyv17fLpAQUX1Ns-MZvQS8prBlvWSf9h7V7YcmOiAy-EJ2TDQqpN87J-SDYBgnQToL8iLUu4BQPYjf04uuNC9Gge5IT--5zSFVIOl6JawhlIz1pBWGlbqMccjjWH27ynWtD-2WB3FUn8u-JEiXXzFDleMxxIKTTO1sa2wGGnNAWN5SZ7NLfyrx7wkt58_3e6-dtc3X77trq47KweonXP95LTkkjE5eWcRRq20cjhZ4YZBiUnZXjPUwqGwM1NsHi06LmeYtARxSd6d1-5z-nXwpZolFOtjxNWnQzFMSsWZZiP7D8q1anrUjb79h96nQ27PnpSAHkAx3lR3VncYvQmrTWv1D9WmGP2dN-3N3Y25ElII1cthaH579janUrKfzT6HBfPRMDCnSs2pUnOq1JwqbQNvHs84TIt3f_mfDsVvxuabGg</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Elazab, Nancy</creator><creator>Mendy, Angelico</creator><creator>Gasana, Janvier</creator><creator>Vieira, Edgar R</creator><creator>Quizon, Annabelle</creator><creator>Forno, Erick</creator><general>American Academy of Pediatrics</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20130901</creationdate><title>Probiotic administration in early life, atopy, and asthma: a meta-analysis of clinical trials</title><author>Elazab, Nancy ; 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However, results from clinical trials have been conflicting, and several of them may have been underpowered. We performed a meta-analysis of randomized, placebo-controlled trials to assess the effects of probiotic supplementation on atopic sensitization and asthma/wheeze prevention in children.
Random-effects models were used to calculate pooled risk estimates. Meta-regression was conducted to examine the effect of potential factors on probiotics efficacy.
Probiotics were effective in reducing total immunoglobulin E (IgE) (mean reduction: -7.59 U/mL [95% confidence interval (CI): -14.96 to -0.22]; P = .044). Meta-regression showed that the reduction in IgE was more pronounced with longer follow-up. Probiotics significantly reduced the risk of atopic sensitization when administered prenatally (relative risk: 0.88 [95% CI: 0.78 to 0.99]; P = .035 for positive result on the skin prick test and/or elevated specific IgE to common allergens) and postnatally (relative risk: 0.86 [95% CI: 0.75 to 0.98]; P = .027 for positive result on skin prick test). Administration of Lactobacillus acidophilus, compared with other strains, was associated with an increased risk of atopic sensitization (P = .002). Probiotics did not significantly reduce asthma/wheeze (relative risk: 0.96 [95% CI: 0.85 to 1.07]).
Prenatal and/or early-life probiotic administration reduces the risk of atopic sensitization and decreases the total IgE level in children but may not reduce the risk of asthma/wheeze. Follow-up duration and strain significantly modified these effects. Future trials for asthma prevention should carefully select probiotic strain and consider longer follow-up.</abstract><cop>United States</cop><pub>American Academy of Pediatrics</pub><pmid>23958764</pmid><doi>10.1542/peds.2013-0246</doi></addata></record> |
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subjects | Adolescent Asthma Asthma - immunology Asthma - prevention & control Asthma in children Care and treatment Child Child, Preschool Childhood asthma Children & youth Clinical trials Dermatitis, Atopic - immunology Dermatitis, Atopic - prevention & control Dosage and administration Double-Blind Method Female Follow-Up Studies Humans Immunoglobulin E - blood Immunoglobulins Infant Infant, Newborn Lactobacillus acidophilus Male Pediatrics Pregnancy Prevention Probiotics Probiotics - administration & dosage Randomized Controlled Trials as Topic Regression analysis Respiratory Hypersensitivity - immunology Respiratory Hypersensitivity - prevention & control Risk Risk assessment Safety and security measures Treatment Outcome |
title | Probiotic administration in early life, atopy, and asthma: a meta-analysis of clinical trials |
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