Erin Pennock, Emma L Slack, Jess A Grebby, Lara N Forster, Mark S Pearce
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Multivariable linear regression was used to examine relationships between infections and cognition. The total number of infections in the first 5 years of life was not significantly associated with IQ, EQ or AQ, nor were there significant relationships between cognitive outcomes and most infections. Tonsillitis did display a positive, significant association with IQ after adjustment for confounders (<i>b</i> = 6.43, 95% CI 0.92, 11.94, <i>p</i> = 0.022). Lower respiratory tract infections (LRTIs) showed significant negative relationships with all cognitive outcomes. <i>H. pylori</i> seropositivity at age 50 exhibited negative, significant relationships with EQ (<i>p</i> = 0.014) and AQ (<i>p</i> = 0.024) after adjustment for confounders. Although no significant relationship between overall infections and cognition were found, there were indications that LRTIs and gastrointestinal system infections may limit cognitive development. Given these infections remain prevalent, further research regarding severity and recurrence of infections and how they affect childhood cognition is needed.</p>","PeriodicalId":49167,"journal":{"name":"Journal of Developmental Origins of Health and Disease","volume":" ","pages":"648-657"},"PeriodicalIF":1.5000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Associations between early infections and childhood cognition in the Newcastle Thousand Families Study birth cohort.\",\"authors\":\"Erin Pennock, Emma L Slack, Jess A Grebby, Lara N Forster, Mark S Pearce\",\"doi\":\"10.1017/S2040174423000338\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Childhood infections have been shown to stunt growth, contribute to malnutrition and reduce cognition in early adulthood. This study aimed to assess relationships between early life infections and childhood cognition at age 11 years in the Newcastle Thousand Families Study (NTFS). The analysis included 741 members from the NTFS who had complete data for infections between birth and 5 years, and the 11-plus examinations. School records from the 11-plus examinations showed cognitive (IQ), English (EQ) and arithmetic (AQ) abilities. Housing conditions, overcrowding, birth order and social class were recorded at birth. <i>Helicobacter pylori</i> seropositivity was measured at age 49-51 years. Multivariable linear regression was used to examine relationships between infections and cognition. The total number of infections in the first 5 years of life was not significantly associated with IQ, EQ or AQ, nor were there significant relationships between cognitive outcomes and most infections. Tonsillitis did display a positive, significant association with IQ after adjustment for confounders (<i>b</i> = 6.43, 95% CI 0.92, 11.94, <i>p</i> = 0.022). Lower respiratory tract infections (LRTIs) showed significant negative relationships with all cognitive outcomes. <i>H. pylori</i> seropositivity at age 50 exhibited negative, significant relationships with EQ (<i>p</i> = 0.014) and AQ (<i>p</i> = 0.024) after adjustment for confounders. Although no significant relationship between overall infections and cognition were found, there were indications that LRTIs and gastrointestinal system infections may limit cognitive development. 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引用次数: 0
摘要
儿童感染已被证明会阻碍生长,导致营养不良,并降低成年早期的认知能力。本研究旨在评估纽卡斯尔千家庭研究(NTFS)中早期生活感染与11岁儿童认知之间的关系。该分析包括来自NTFS的741名成员,他们拥有从出生到5岁的完整感染数据,以及11次以上的检查。11 +考试的学校记录显示了认知(IQ)、英语(EQ)和算术(AQ)能力。出生时记录了住房条件、拥挤程度、出生顺序和社会阶层。49-51岁时检测幽门螺杆菌血清阳性。多变量线性回归用于检验感染与认知之间的关系。前5年感染的总数与智商、情商或智商没有显著相关性,认知结果与大多数感染之间也没有显著相关性。调整混杂因素后,扁桃体炎确实与智商呈显著正相关(b = 6.43, 95% CI 0.92, 11.94, p = 0.022)。下呼吸道感染(LRTIs)与所有认知结果呈显著负相关。校正混杂因素后,50岁时幽门螺杆菌血清阳性与EQ (p = 0.014)和AQ (p = 0.024)呈显著负相关。虽然总体感染与认知之间没有明显的关系,但有迹象表明,下呼吸道感染和胃肠道系统感染可能限制认知发展。鉴于这些感染仍然普遍存在,需要进一步研究感染的严重程度和复发以及它们如何影响儿童认知。
Associations between early infections and childhood cognition in the Newcastle Thousand Families Study birth cohort.
Childhood infections have been shown to stunt growth, contribute to malnutrition and reduce cognition in early adulthood. This study aimed to assess relationships between early life infections and childhood cognition at age 11 years in the Newcastle Thousand Families Study (NTFS). The analysis included 741 members from the NTFS who had complete data for infections between birth and 5 years, and the 11-plus examinations. School records from the 11-plus examinations showed cognitive (IQ), English (EQ) and arithmetic (AQ) abilities. Housing conditions, overcrowding, birth order and social class were recorded at birth. Helicobacter pylori seropositivity was measured at age 49-51 years. Multivariable linear regression was used to examine relationships between infections and cognition. The total number of infections in the first 5 years of life was not significantly associated with IQ, EQ or AQ, nor were there significant relationships between cognitive outcomes and most infections. Tonsillitis did display a positive, significant association with IQ after adjustment for confounders (b = 6.43, 95% CI 0.92, 11.94, p = 0.022). Lower respiratory tract infections (LRTIs) showed significant negative relationships with all cognitive outcomes. H. pylori seropositivity at age 50 exhibited negative, significant relationships with EQ (p = 0.014) and AQ (p = 0.024) after adjustment for confounders. Although no significant relationship between overall infections and cognition were found, there were indications that LRTIs and gastrointestinal system infections may limit cognitive development. Given these infections remain prevalent, further research regarding severity and recurrence of infections and how they affect childhood cognition is needed.
期刊介绍:
JDOHaD publishes leading research in the field of Developmental Origins of Health and Disease (DOHaD). The Journal focuses on the environment during early pre-natal and post-natal animal and human development, interactions between environmental and genetic factors, including environmental toxicants, and their influence on health and disease risk throughout the lifespan. JDOHaD publishes work on developmental programming, fetal and neonatal biology and physiology, early life nutrition, especially during the first 1,000 days of life, human ecology and evolution and Gene-Environment Interactions.
JDOHaD also accepts manuscripts that address the social determinants or education of health and disease risk as they relate to the early life period, as well as the economic and health care costs of a poor start to life. Accordingly, JDOHaD is multi-disciplinary, with contributions from basic scientists working in the fields of physiology, biochemistry and nutrition, endocrinology and metabolism, developmental biology, molecular biology/ epigenetics, human biology/ anthropology, and evolutionary developmental biology. Moreover clinicians, nutritionists, epidemiologists, social scientists, economists, public health specialists and policy makers are very welcome to submit manuscripts.
The journal includes original research articles, short communications and reviews, and has regular themed issues, with guest editors; it is also a platform for conference/workshop reports, and for opinion, comment and interaction.