Switkowski Karen M, Oken Emily, Simonin Elisabeth M, Nadeau Kari C, Rifas-Shiman Sheryl L, Lightdale Jenifer R
Division of Chronic Disease Research Across the Lifecourse, Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, MA.
Division of Chronic Disease Research Across the Lifecourse, Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, MA; Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA.
J Pediatr. 2025 Apr 23;283:114623. doi: 10.1016/j.jpeds.2025.114623.
To assess the extent to which risks of atopic and respiratory conditions throughout childhood and adolescence differ by history of (1) infant colic, characterized by apparent abdominal discomfort and unsoothable crying, (2) excessive crying without colic, or (3) neither condition.
Among 1249 children participating in the prospective, unselected Project Viva cohort, we examined associations of history of infant colic or excessive crying without colic with risks of eczema, allergic rhinitis, asthma, and respiratory infections, measured in toddlerhood, early childhood, mid-childhood, early adolescence, and mid-adolescence using multinomial logistic regression models.
The study sample was 50% female and 71% non-Hispanic White; 26% had colic and 9% excessive crying. Children with colic (vs no colic or excessive crying) had higher risk of eczema (relative risk ratio [RRR], 2.1; 95% CI, 1.2-3.8), allergic rhinitis (RRR, 1.6; 95% CI, 1.1-2.4), and asthma (RRR, 1.6; 95% CI,1.1-2.4) in mid-childhood, and a higher risk of respiratory infections in toddlerhood (RRR, 1.6; 95% CI, 1.2-2.2) and mid-adolescence (RRR, 2.1; 95% CI, 1.2, 3.7). The risk of 2-3 concurrent atopic conditions (eczema, allergic rhinitis, and/or asthma) was nearly twice that among the colic group (vs unaffected) at all life stages. The group with excessive crying without colic did not have increased risk of atopic and respiratory outcomes.
Colic characterized by unsoothable crying and parent perceptions of abdominal distress may be an early marker of atopic susceptibility.
评估在整个儿童期和青少年期,(1)以明显腹部不适和难以安抚的哭闹为特征的婴儿腹绞痛病史、(2)无腹绞痛的过度哭闹病史或(3)无上述两种情况的病史,对特应性疾病和呼吸道疾病风险的影响程度。
在参与前瞻性、未经过筛选的活力项目队列研究的1249名儿童中,我们使用多项逻辑回归模型,研究婴儿腹绞痛病史或无腹绞痛的过度哭闹病史与湿疹、过敏性鼻炎、哮喘和呼吸道感染风险之间的关联,这些疾病风险在幼儿期、儿童早期、儿童中期、青少年早期和青少年中期进行测量。
研究样本中50%为女性,71%为非西班牙裔白人;26%有腹绞痛,9%有过度哭闹。有腹绞痛的儿童(与无腹绞痛或过度哭闹的儿童相比)在儿童中期患湿疹(相对风险比[RRR],2.1;95%置信区间[CI],1.2 - 3.8)、过敏性鼻炎(RRR,1.6;95% CI,1.1 - 2.4)和哮喘(RRR,1.6;95% CI,1.1 - 2.4)的风险更高,在幼儿期(RRR,1.6;95% CI,1.2 - 2.2)和青少年中期(RRR,2.1;95% CI,1.2,3.7)患呼吸道感染的风险更高。在所有生命阶段,同时患有2 - 3种特应性疾病(湿疹、过敏性鼻炎和/或哮喘)的风险在腹绞痛组(与未受影响组相比)几乎是两倍。无腹绞痛的过度哭闹组患特应性疾病和呼吸道疾病的风险没有增加。
以难以安抚的哭闹和家长感知的腹部不适为特征的腹绞痛可能是特应性易感性的早期标志。