Abstract:Objective To study the association of blood lipids with the development, clinical stage, allergic condition, and pulmonary function of asthma. Methods A total of 56 children with asthma who attended the hospital between October 2016 and March 2017 were enrolled as the asthma group, and 46 children who underwent physical examination as the healthy control group. According to the clinical manifestations, the children with asthma were divided into acute exacerbation group (n=24) and chronic persistent group (n=32). According to the results of skin prick test (SPT) and serum IgE measurement, the children with asthma were divided into non-allergic asthma group (n=16) and allergic asthma group (n=38). Fasting blood lipid levels were measured in both asthma and control groups. Pulmonary function tests were performed for asthmatic children. Results There were no significant differences in blood lipid levels between the asthma and control groups (P > 0.05). The acute exacerbation group had significantly lower serum levels of high-density lipoprotein (HDL) and total cholesterol compared with the control group and the chronic persistent group (P < 0.05). The allergic asthma group had a significantly lower serum HDL level than the non-allergic asthma group (P < 0.05). In asthmatic children aged 6-13 years, the ratios of the measured values to the predicted values for forced vital capacity, peak expiratory flow, and maximal expiratory flow at 50% of vital capacity had a linear regression relationship with HDL and were positively correlated with HDL (P < 0.05). Forced expiratory volume in one second and maximal mid-expiratory flow had a linear regression relationship with both HDL and LDL and were positively correlated with them (P < 0.05). Conclusions Blood lipids are associated with the clinical stage, allergic condition, and lung function of childhood asthma. This indicates that blood lipids may be involved in several aspects of the pathogenesis of childhood asthma.
Johnson JB, Summer W, Cutler RG, et al. Alternate day calorie restriction improves clinical findings and reduces markers of oxidative stress and inflammation in overweight adults with moderate asthma[J]. Free Radic Biol Med, 2007, 42(5):665-674.
[2]
Peng J, Huang Y. Meta-analysis of the association between asthma and serum levels of high-density lipoprotein cholesterol and low-density lipoprotein cholesterol[J]. Ann Allergy Asthma Immunol, 2017, 118(1):61-65.
[3]
Su X, Ren Y, Li M, et al. Association between lipid profile and the prevalence of asthma:a meta-analysis and systemic review[J]. Curr Med Res Opin, 2018, 34(3):423-433.
[4]
Yiallouros PK, Savva SC, Kolokotroni O, et al. Low serum high-density lipoprotein cholesterol in childhood is associated with adolescent asthma[J]. Clin Exp Allergy, 2012, 42(3):423-432.
[5]
Yiallouros PK, Savva SC, Kolokotroni O, et al. Asthma:the role of low high-density-lipoprotein cholesterol in childhood and adolescence[J]. Int Arch Allergy Immunol, 2014, 165(2):91-99.
[6]
Vinding RK, Stokholm J, Chawes BLK, et al. Blood lipid levels associate with childhood asthma, airway obstruction, bronchial hyperresponsiveness, and aeroallergen sensitization[J]. J Allergy Clin Immunol, 2016, 137(1):68-74.e4.
[7]
Global Initiative for Asthma. Global strategy for asthma management and prevention[DB/OL]. (2016-4-24).
[8]
Gordon EM, Figueroa DM, Barochia AV, et al. High-density lipoproteins and apolipoprotein A-I:potential new players in the prevention and treatment of lung disease[J]. Front Pharmacol, 2016, 7:323.
[9]
Cirillo DJ, Agrawal Y, Cassano PA. Lipids and pulmonary function in the third national health and nutrition examination survey[J]. Am J Epidemiol, 2002, 155(9):842-848.
[10]
Barochia AV, Kaler M, Cuento RA, et al. Serum apolipoprotein A-I and large high-density lipoprotein particles are positively correlated with FEV1 in atopic asthma[J]. Am J Respir Crit Care Med, 2015, 191(9):990-1000.
[11]
Rastogi D, Jung M, Strizich G, et al. Association of systemic inflammation, adiposity, and metabolic dysregulation with asthma burden among Hispanic adults[J]. Respir Med, 2017, 125:72-81.
[12]
Rastogi D, Fraser S, Oh J, et al. Inflammation, metabolic dysregulation, and pulmonary function among obese urban adolescents with asthma[J]. Am J Respir Crit Care Med, 2015, 191(2):149-160.
[13]
Becker KG. The common variants/multiple disease hypothesis of common complex genetic disorders[J]. Med Hypotheses, 2004, 62(2):309-317.
[14]
Yiallouros PK, Kouis P, Kolokotroni O, et al. Shared genetic variants between serum levels of high-density lipoprotein cholesterol and wheezing in a cohort of children from Cyprus[J]. Ital J Pediatr, 2016, 42(1):67.
[15]
Skaaby T, Husemoen LL, Martinussen T, et al. Vitamin D status, filaggrin genotype, and cardiovascular risk factors:a Mendelian randomization approach[J]. PLoS One, 2013, 8(2):e57647.
[16]
Ouyang F, Kumar R, Pongracic J, et al. Adiposity, serum lipid levels, and allergic sensitization in Chinese men and women[J]. J Allergy Clin Immunol, 2009, 123(4):940-948.e10.
[17]
Robertson AK, Zhou X, Strandvik B, et al. Severe hypercholesterolaemia leads to strong Th2 responses to an exogenous antigen[J]. Scand J Immunol, 2004, 59(3):285-293.
[18]
Zhou X, Paulsson G, Stemme S, et al. Hypercholesterolemia is associated with a T helper (Th)1/Th2 switch of the autoimmune response in atherosclerotic apo E-knockout mice[J]. J Clin Invest, 1998, 101(8):1717-1725.
[19]
Manti S, Leonardi S, Panasiti I, et al. Serum IL-10, IL-17 and IL-23 levels as "bioumoral bridges" between dyslipidemia and atopy[J]. Cytokine, 2017, 99:43-49.
[20]
Nandedkar SD, Weihrauch D, Xu H, et al. D-4F, an apoA-1 mimetic, decreases airway hyperresponsiveness, inflammation, and oxidative stress in a murine model of asthma[J]. J Lipid Res, 2011, 52(3):499-508.