2015
DOI: 10.1111/all.12783
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Heritability and confirmation of genetic association studies for childhood asthma in twins

Abstract: Asthma and allergic diseases of childhood are highly heritable, and these high-risk genetic variants associated specifically with childhood asthma, except for one SNP shared with hay fever.

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Cited by 86 publications
(73 citation statements)
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“…It is well known that a parental history of allergy is an important risk factor for asthma, allergic symptoms, and sensitization. 32,33 In this study, we found that parental asthma increased the risk of asthma in the children, while parental hay fever increased their risk of hay fever, cat allergy, and for paternal hay fever even dog allergy.…”
Section: Discussionsupporting
confidence: 47%
“…It is well known that a parental history of allergy is an important risk factor for asthma, allergic symptoms, and sensitization. 32,33 In this study, we found that parental asthma increased the risk of asthma in the children, while parental hay fever increased their risk of hay fever, cat allergy, and for paternal hay fever even dog allergy.…”
Section: Discussionsupporting
confidence: 47%
“…We have previously validated the register-based comparison variable "register-based ever asthma" against medical records with high positive predictive values (0.89 95% CI: 0.85-0.92) for clinical asthma diagnosis. 21 This definition of asthma has been applied in several studies as a proxy for ever/incident asthma [29][30][31][32][33] as well as for current/prevalent asthma. 30 Another study investigating "reported doctor's diagnosis" found a moderate PPV of 0.57 when the question of parental-reported doctor's diagnosis was validated against asthma medication reimbursement in a younger cohort.…”
Section: Discussionmentioning
confidence: 99%
“…A study in twins with childhood asthma showed that allergic diseases of childhood are highly heritable. 14 In this study, the authors found that the SNP rs3771180 in IL1RL1 is associated both with asthma and with AR. 14 Kurakula et al 15 found that the SNP rs4851765 in FHL2 shows an association with the severity of bronchial hyper-responsiveness, identifying FHL2 as a novel gene associated with asthma severity in humans.…”
mentioning
confidence: 67%