NSAID Use and the Risk of Parkinson's Disease: Systematic Review and Meta-Analysis of Observational Studies
Identifieur interne : 000511 ( PascalFrancis/Corpus ); précédent : 000510; suivant : 000512NSAID Use and the Risk of Parkinson's Disease: Systematic Review and Meta-Analysis of Observational Studies
Auteurs : Ali Samii ; Mahyar Etminan ; Matthew O. Wiens ; Siavash JafariSource :
- Drugs & aging [ 1170-229X ] ; 2009.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Background: Several studies have suggested that NSAID use may modify the risk of developing Parkinson's disease (PD). Objective: Our aim was to conduct a meta-analysis of observational studies evaluating NSAID use and the risk of PD. Methods: We systematically searched MEDLINE (1966-November 2008), EMBASE (1980-November 2008) and other databases. Data from 11 studies were included in the meta-analysis. We used the random effects model to calculate risk ratios (relative risks) and their corresponding 95% confidence intervals (CIs). Results: The pooled risk ratio of PD with NSAID use was 0.95 (95% CI 0.80, 1.12). The pooled risk ratio of PD with high-dose or long-duration NSAID use was 0.91 (95% CI 0.78, 1.05). The pooled risk ratio of PD for aspirin (acetylsalicylic acid) users was 1.08 (95% CI 0.93, 1.26). The pooled risk ratio of PD among ibuprofen users was 0.76 (95% CI 0.65, 0.89). The pooled risk ratio of PD in men using NSAIDs was 0.79 (95% CI 0.69, 0.92), and in women using NSAIDs, it was 0.72 (95% CI 0.45, 1.15). Conclusions: NSAIDs as a class do not seem to modify the risk of PD. However, ibuprofen may have a slight protective effect in lowering the risk of PD. Although the risk ratios of PD in male and female NSAID users were similar, the 95% CI for men was suggestive of a slight risk reduction.
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Pour connaître la documentation sur le format Inist Standard.
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Format Inist (serveur)
NO : | PASCAL 09-0427296 INIST |
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ET : | NSAID Use and the Risk of Parkinson's Disease: Systematic Review and Meta-Analysis of Observational Studies |
AU : | SAMII (Ali); ETMINAN (Mahyar); WIENS (Matthew O.); JAFARI (Siavash) |
AF : | Department of Neurology, University of Washington, and the Seattle VA Parkinson Disease Research Education and Clinical Center/Seattle, Washington/Etats-Unis (1 aut.); Centre for Clinical Epidemiology and Evaluation, Department of Medicine, Faculty of Medicine, University of British Columbia/Vancouver, British Columbia/Canada (2 aut.); Faculty of Pharmaceutical Sciences, University of British Columbia/Vancouver, British Columbia/Canada (3 aut.); Chilliwack General Hospital/Chilliwack, British Columbia/Canada (3 aut.); School of Population and Public Health, University of British Columbia/Vancouver, British Columbia/Canada (4 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Drugs & aging; ISSN 1170-229X; Nouvelle-Zélande; Da. 2009; Vol. 26; No. 9; Pp. 769-779; Bibl. 28 ref. |
LA : | Anglais |
EA : | Background: Several studies have suggested that NSAID use may modify the risk of developing Parkinson's disease (PD). Objective: Our aim was to conduct a meta-analysis of observational studies evaluating NSAID use and the risk of PD. Methods: We systematically searched MEDLINE (1966-November 2008), EMBASE (1980-November 2008) and other databases. Data from 11 studies were included in the meta-analysis. We used the random effects model to calculate risk ratios (relative risks) and their corresponding 95% confidence intervals (CIs). Results: The pooled risk ratio of PD with NSAID use was 0.95 (95% CI 0.80, 1.12). The pooled risk ratio of PD with high-dose or long-duration NSAID use was 0.91 (95% CI 0.78, 1.05). The pooled risk ratio of PD for aspirin (acetylsalicylic acid) users was 1.08 (95% CI 0.93, 1.26). The pooled risk ratio of PD among ibuprofen users was 0.76 (95% CI 0.65, 0.89). The pooled risk ratio of PD in men using NSAIDs was 0.79 (95% CI 0.69, 0.92), and in women using NSAIDs, it was 0.72 (95% CI 0.45, 1.15). Conclusions: NSAIDs as a class do not seem to modify the risk of PD. However, ibuprofen may have a slight protective effect in lowering the risk of PD. Although the risk ratios of PD in male and female NSAID users were similar, the 95% CI for men was suggestive of a slight risk reduction. |
CC : | 002B02B05; 002B17G; 002B17A01 |
FD : | Antiinflammatoire non stéroïde; Facteur risque; Maladie de Parkinson; Revue systématique; Article synthèse; Métaanalyse; Personne âgée; Ibuprofène; Acide acétylsalicylique; Analgésique; Antipyrétique; Inhibiteur thromboagrégation; Risque relatif |
FG : | Homme; Maladie dégénérative; Pathologie du système nerveux; Pathologie de l'encéphale; Syndrome extrapyramidal; Pathologie du système nerveux central; Dérivé de l'acide arylpropionique; Inhibiteur enzyme; Prostaglandin-endoperoxide synthase; Oxidoreductases; Enzyme; Salicylés |
ED : | Non steroidal antiinflammatory agent; Risk factor; Parkinson disease; Systematic review; Review; Metaanalysis; Elderly; Ibuprofen; Acetylsalicylic acid; Analgesic; Antipyretic; Antiplatelet agent; Relative risk |
EG : | Human; Degenerative disease; Nervous system diseases; Cerebral disorder; Extrapyramidal syndrome; Central nervous system disease; Arylpropionic acid derivatives; Enzyme inhibitor; Prostaglandin-endoperoxide synthase; Oxidoreductases; Enzyme; Salicylates |
SD : | Antiinflamatorio no esteroide; Factor riesgo; Parkinson enfermedad; Revisión sistemática; Artículo síntesis; Meta-análisis; Anciano; Ibuprofeno; Acetilsalicilico ácido; Analgésico; Antipirético; Inhibidor tromboagregación |
LO : | INIST-26115.354000170024200040 |
ID : | 09-0427296 |
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Pascal:09-0427296Le document en format XML
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<front><div type="abstract" xml:lang="en">Background: Several studies have suggested that NSAID use may modify the risk of developing Parkinson's disease (PD). Objective: Our aim was to conduct a meta-analysis of observational studies evaluating NSAID use and the risk of PD. Methods: We systematically searched MEDLINE (1966-November 2008), EMBASE (1980-November 2008) and other databases. Data from 11 studies were included in the meta-analysis. We used the random effects model to calculate risk ratios (relative risks) and their corresponding 95% confidence intervals (CIs). Results: The pooled risk ratio of PD with NSAID use was 0.95 (95% CI 0.80, 1.12). The pooled risk ratio of PD with high-dose or long-duration NSAID use was 0.91 (95% CI 0.78, 1.05). The pooled risk ratio of PD for aspirin (acetylsalicylic acid) users was 1.08 (95% CI 0.93, 1.26). The pooled risk ratio of PD among ibuprofen users was 0.76 (95% CI 0.65, 0.89). The pooled risk ratio of PD in men using NSAIDs was 0.79 (95% CI 0.69, 0.92), and in women using NSAIDs, it was 0.72 (95% CI 0.45, 1.15). Conclusions: NSAIDs as a class do not seem to modify the risk of PD. However, ibuprofen may have a slight protective effect in lowering the risk of PD. Although the risk ratios of PD in male and female NSAID users were similar, the 95% CI for men was suggestive of a slight risk reduction.</div>
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<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Pathologie du système nerveux</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Pathologie de l'encéphale</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Syndrome extrapyramidal</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Pathologie du système nerveux central</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Dérivé de l'acide arylpropionique</s0>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Arylpropionic acid derivatives</s0>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Arilpropionico ácido derivado</s0>
<s5>42</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Inhibiteur enzyme</s0>
<s5>43</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Enzyme inhibitor</s0>
<s5>43</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Inhibidor enzima</s0>
<s5>43</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Prostaglandin-endoperoxide synthase</s0>
<s2>FE</s2>
<s5>44</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Prostaglandin-endoperoxide synthase</s0>
<s2>FE</s2>
<s5>44</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Prostaglandin-endoperoxide synthase</s0>
<s2>FE</s2>
<s5>44</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="11" i2="X" l="SPA"><s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="12" i2="X" l="FRE"><s0>Salicylés</s0>
<s5>45</s5>
</fC07>
<fC07 i1="12" i2="X" l="ENG"><s0>Salicylates</s0>
<s5>45</s5>
</fC07>
<fC07 i1="12" i2="X" l="SPA"><s0>Salicilatos</s0>
<s5>45</s5>
</fC07>
<fN21><s1>306</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 09-0427296 INIST</NO>
<ET>NSAID Use and the Risk of Parkinson's Disease: Systematic Review and Meta-Analysis of Observational Studies</ET>
<AU>SAMII (Ali); ETMINAN (Mahyar); WIENS (Matthew O.); JAFARI (Siavash)</AU>
<AF>Department of Neurology, University of Washington, and the Seattle VA Parkinson Disease Research Education and Clinical Center/Seattle, Washington/Etats-Unis (1 aut.); Centre for Clinical Epidemiology and Evaluation, Department of Medicine, Faculty of Medicine, University of British Columbia/Vancouver, British Columbia/Canada (2 aut.); Faculty of Pharmaceutical Sciences, University of British Columbia/Vancouver, British Columbia/Canada (3 aut.); Chilliwack General Hospital/Chilliwack, British Columbia/Canada (3 aut.); School of Population and Public Health, University of British Columbia/Vancouver, British Columbia/Canada (4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Drugs & aging; ISSN 1170-229X; Nouvelle-Zélande; Da. 2009; Vol. 26; No. 9; Pp. 769-779; Bibl. 28 ref.</SO>
<LA>Anglais</LA>
<EA>Background: Several studies have suggested that NSAID use may modify the risk of developing Parkinson's disease (PD). Objective: Our aim was to conduct a meta-analysis of observational studies evaluating NSAID use and the risk of PD. Methods: We systematically searched MEDLINE (1966-November 2008), EMBASE (1980-November 2008) and other databases. Data from 11 studies were included in the meta-analysis. We used the random effects model to calculate risk ratios (relative risks) and their corresponding 95% confidence intervals (CIs). Results: The pooled risk ratio of PD with NSAID use was 0.95 (95% CI 0.80, 1.12). The pooled risk ratio of PD with high-dose or long-duration NSAID use was 0.91 (95% CI 0.78, 1.05). The pooled risk ratio of PD for aspirin (acetylsalicylic acid) users was 1.08 (95% CI 0.93, 1.26). The pooled risk ratio of PD among ibuprofen users was 0.76 (95% CI 0.65, 0.89). The pooled risk ratio of PD in men using NSAIDs was 0.79 (95% CI 0.69, 0.92), and in women using NSAIDs, it was 0.72 (95% CI 0.45, 1.15). Conclusions: NSAIDs as a class do not seem to modify the risk of PD. However, ibuprofen may have a slight protective effect in lowering the risk of PD. Although the risk ratios of PD in male and female NSAID users were similar, the 95% CI for men was suggestive of a slight risk reduction.</EA>
<CC>002B02B05; 002B17G; 002B17A01</CC>
<FD>Antiinflammatoire non stéroïde; Facteur risque; Maladie de Parkinson; Revue systématique; Article synthèse; Métaanalyse; Personne âgée; Ibuprofène; Acide acétylsalicylique; Analgésique; Antipyrétique; Inhibiteur thromboagrégation; Risque relatif</FD>
<FG>Homme; Maladie dégénérative; Pathologie du système nerveux; Pathologie de l'encéphale; Syndrome extrapyramidal; Pathologie du système nerveux central; Dérivé de l'acide arylpropionique; Inhibiteur enzyme; Prostaglandin-endoperoxide synthase; Oxidoreductases; Enzyme; Salicylés</FG>
<ED>Non steroidal antiinflammatory agent; Risk factor; Parkinson disease; Systematic review; Review; Metaanalysis; Elderly; Ibuprofen; Acetylsalicylic acid; Analgesic; Antipyretic; Antiplatelet agent; Relative risk</ED>
<EG>Human; Degenerative disease; Nervous system diseases; Cerebral disorder; Extrapyramidal syndrome; Central nervous system disease; Arylpropionic acid derivatives; Enzyme inhibitor; Prostaglandin-endoperoxide synthase; Oxidoreductases; Enzyme; Salicylates</EG>
<SD>Antiinflamatorio no esteroide; Factor riesgo; Parkinson enfermedad; Revisión sistemática; Artículo síntesis; Meta-análisis; Anciano; Ibuprofeno; Acetilsalicilico ácido; Analgésico; Antipirético; Inhibidor tromboagregación</SD>
<LO>INIST-26115.354000170024200040</LO>
<ID>09-0427296</ID>
</server>
</inist>
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