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Medical History, Lifestyle, Family History, and Occupational Risk Factors for Marginal Zone Lymphoma: The InterLymph Non-Hodgkin Lymphoma Subtypes Project

Identifieur interne : 003729 ( Main/Exploration ); précédent : 003728; suivant : 003730

Medical History, Lifestyle, Family History, and Occupational Risk Factors for Marginal Zone Lymphoma: The InterLymph Non-Hodgkin Lymphoma Subtypes Project

Auteurs : Paige M. Bracci ; Yolanda Benavente ; Jennifer J. Turner ; Ora Paltiel ; Susan L. Slager ; Claire M. Vajdic ; Aaron D. Norman ; James R. Cerhan ; Brian C. H. Chiu ; Nikolaus Becker ; Pierluigi Cocco ; Ahmet Dogan ; Alexandra Nieters ; Elizabeth A. Holly ; Eleanor V. Kane ; Karin E. Smedby ; Marc Maynadié ; John J. Spinelli ; Eve Roman ; Bengt Glimelius ; Sophia S. Wang ; Joshua N. Sampson ; Lindsay M. Morton ; Silvia De Sanjosé

Source :

RBID : PMC:4207869

Descripteurs français

English descriptors

Abstract

Background

Marginal zone lymphoma (MZL), comprised of nodal, extranodal, and splenic subtypes, accounts for 5%–10% of non-Hodgkin lymphoma cases. A detailed evaluation of the independent effects of risk factors for MZL and its subtypes has not been conducted.

Methods

Data were pooled from 1052 MZL cases (extranodal [EMZL] = 633, nodal [NMZL] = 157, splenic [SMZL] = 140) and 13766 controls from 12 case–control studies. Adjusted unconditional logistic regression was used to compute odds ratios (ORs) and 95% confidence intervals (CIs).

Results

Novel findings for MZL subtypes include increased risk for B-cell activating autoimmune conditions (EMZL OR = 6.40, 95% CI = 4.24 to 9.68; NMZL OR = 7.80, 95% CI = 3.32 to 18.33; SMZL OR = 4.25, 95% CI = 1.49 to 12.14), hepatitis C virus seropositivity (EMZL OR = 5.29, 95% CI = 2.48 to 11.28), self-reported peptic ulcers (EMZL OR = 1.83, 95% CI = 1.35 to 2.49), asthma without other atopy (SMZL OR = 2.28, 95% CI = 1.23 to 4.23), family history of hematologic cancer (EMZL OR = 1.90, 95% CI = 1.37 to 2.62) and of non-Hodgkin lymphoma (NMZL OR = 2.82, 95% CI = 1.33 to 5.98), permanent hairdye use (SMZL OR = 6.59, 95% CI = 1.54 to 28.17), and occupation as a metalworker (NMZL OR = 3.56, 95% CI = 1.67 to 7.58). Reduced risks were observed with consumption of any alcohol (EMZL fourth quartile OR = 0.48, 95% CI = 0.28 to 0.82) and lower consumption of wine (NMZL first to third quartile ORs < 0.45) compared with nondrinkers, and occupation as a teacher (EMZL OR = 0.58, 95% CI = 0.37 to 0.88).

Conclusion

Our results provide new data suggesting etiologic heterogeneity across MZL subtypes although a common risk of MZL associated with B-cell activating autoimmune conditions was found.


Url:
DOI: 10.1093/jncimonographs/lgu011
PubMed: 25174026
PubMed Central: 4207869


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title level="j">Journal of the National Cancer Institute. Monographs</title>
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<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Australia (epidemiology)</term>
<term>Australia (ethnology)</term>
<term>Case-Control Studies</term>
<term>Comorbidity</term>
<term>Europe (epidemiology)</term>
<term>Europe (ethnology)</term>
<term>Female</term>
<term>Humans</term>
<term>Life Style</term>
<term>Lymphoma, B-Cell, Marginal Zone (diagnosis)</term>
<term>Lymphoma, B-Cell, Marginal Zone (epidemiology)</term>
<term>Lymphoma, B-Cell, Marginal Zone (etiology)</term>
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<term>Middle Aged</term>
<term>North America (epidemiology)</term>
<term>North America (ethnology)</term>
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<term>Odds Ratio</term>
<term>Risk Factors</term>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
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<term>Australie (épidémiologie)</term>
<term>Comorbidité</term>
<term>Europe (ethnologie)</term>
<term>Europe (épidémiologie)</term>
<term>Exposition professionnelle</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Lymphome B de la zone marginale (diagnostic)</term>
<term>Lymphome B de la zone marginale (épidémiologie)</term>
<term>Lymphome B de la zone marginale (étiologie)</term>
<term>Mode de vie</term>
<term>Mâle</term>
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<term>Sujet âgé de 80 ans ou plus</term>
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<term>Europe</term>
<term>North America</term>
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<term>Australie</term>
<term>Europe</term>
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<term>Lymphoma, B-Cell, Marginal Zone</term>
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<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Amérique du Nord</term>
<term>Australie</term>
<term>Europe</term>
<term>Lymphome B de la zone marginale</term>
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<term>Lymphome B de la zone marginale</term>
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<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Case-Control Studies</term>
<term>Comorbidity</term>
<term>Female</term>
<term>Humans</term>
<term>Life Style</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Occupational Exposure</term>
<term>Odds Ratio</term>
<term>Risk Factors</term>
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<term>Adulte d'âge moyen</term>
<term>Comorbidité</term>
<term>Exposition professionnelle</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Mode de vie</term>
<term>Mâle</term>
<term>Odds ratio</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Études cas-témoins</term>
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<div type="abstract" xml:lang="en">
<sec>
<title>Background</title>
<p>Marginal zone lymphoma (MZL), comprised of nodal, extranodal, and splenic subtypes, accounts for 5%–10% of non-Hodgkin lymphoma cases. A detailed evaluation of the independent effects of risk factors for MZL and its subtypes has not been conducted.</p>
</sec>
<sec>
<title>Methods</title>
<p>Data were pooled from 1052 MZL cases (extranodal [EMZL] = 633, nodal [NMZL] = 157, splenic [SMZL] = 140) and 13766 controls from 12 case–control studies. Adjusted unconditional logistic regression was used to compute odds ratios (ORs) and 95% confidence intervals (CIs).</p>
</sec>
<sec>
<title>Results</title>
<p>Novel findings for MZL subtypes include increased risk for B-cell activating autoimmune conditions (EMZL OR = 6.40, 95% CI = 4.24 to 9.68; NMZL OR = 7.80, 95% CI = 3.32 to 18.33; SMZL OR = 4.25, 95% CI = 1.49 to 12.14), hepatitis C virus seropositivity (EMZL OR = 5.29, 95% CI = 2.48 to 11.28), self-reported peptic ulcers (EMZL OR = 1.83, 95% CI = 1.35 to 2.49), asthma without other atopy (SMZL OR = 2.28, 95% CI = 1.23 to 4.23), family history of hematologic cancer (EMZL OR = 1.90, 95% CI = 1.37 to 2.62) and of non-Hodgkin lymphoma (NMZL OR = 2.82, 95% CI = 1.33 to 5.98), permanent hairdye use (SMZL OR = 6.59, 95% CI = 1.54 to 28.17), and occupation as a metalworker (NMZL OR = 3.56, 95% CI = 1.67 to 7.58). Reduced risks were observed with consumption of any alcohol (EMZL fourth quartile OR = 0.48, 95% CI = 0.28 to 0.82) and lower consumption of wine (NMZL first to third quartile ORs < 0.45) compared with nondrinkers, and occupation as a teacher (EMZL OR = 0.58, 95% CI = 0.37 to 0.88).</p>
</sec>
<sec>
<title>Conclusion</title>
<p>Our results provide new data suggesting etiologic heterogeneity across MZL subtypes although a common risk of MZL associated with B-cell activating autoimmune conditions was found.</p>
</sec>
</div>
</front>
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<name sortKey="Sampson, Joshua N" sort="Sampson, Joshua N" uniqKey="Sampson J" first="Joshua N." last="Sampson">Joshua N. Sampson</name>
<name sortKey="Slager, Susan L" sort="Slager, Susan L" uniqKey="Slager S" first="Susan L." last="Slager">Susan L. Slager</name>
<name sortKey="Smedby, Karin E" sort="Smedby, Karin E" uniqKey="Smedby K" first="Karin E." last="Smedby">Karin E. Smedby</name>
<name sortKey="Spinelli, John J" sort="Spinelli, John J" uniqKey="Spinelli J" first="John J." last="Spinelli">John J. Spinelli</name>
<name sortKey="Turner, Jennifer J" sort="Turner, Jennifer J" uniqKey="Turner J" first="Jennifer J." last="Turner">Jennifer J. Turner</name>
<name sortKey="Vajdic, Claire M" sort="Vajdic, Claire M" uniqKey="Vajdic C" first="Claire M." last="Vajdic">Claire M. Vajdic</name>
<name sortKey="Wang, Sophia S" sort="Wang, Sophia S" uniqKey="Wang S" first="Sophia S." last="Wang">Sophia S. Wang</name>
</noCountry>
</tree>
</affiliations>
</record>

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