Lapinleimu H, Viikari J, Rönnemaa T, Välimäki I, Tuominen J, Marniemi J, Ehnholm C, Jokinen E, Simell O
Cardiorespiratory Research Unit, University of Turku, Finland.
Pediatrics. 1996 Oct;98(4 Pt 1):757-62.
The inherited apolipoprotein E (apoE) phenotype may determine effectiveness of dietary atherosclerosis prevention. This study analyzes the effects of apoE phenotypes on changes in serum lipid concentrations in a 6-month prospective, randomized trial of a low-saturated-fat, low-cholesterol diet in infancy.
One thousand sixty-two healthy infants were randomized to intervention and control groups at the age of 7 months. Counseling was provided to the intervention families when the children's ages were 7, 8, and 10 months. Dietary goals were the child's intake of energy ad libitum, fat at 30% to 35% of energy, cholesterol at less than 200 mg/d, and saturated, monounsaturated, and polyunsaturated fatty acids at a 1:1:1 ratio. Control families consumed an unrestricted diet. The apoE phenotype of 846 of the infants was determined; serum lipid and lipoprotein concentrations were measured at 7 and 13 months of age; and nutrient intakes were analyzed using 3-day food records at 8 and 13 months of age.
At 7 months of age, serum cholesterol concentration was higher in apoE4-positive infants (E2/E4, E3/E4, and homozygous E4) than in apoE4-negative infants (159 +/- 31 mg/dL [4.10 +/- 0.81 mmol/L] vs 150 +/- 29 mg/dL [3.89 +/- 0.74 mmol/L]). The high-density lipoprotein cholesterol concentration was slightly lower in apoE4-positive infants than in apoE4-negative infants (34 +/- 8 mg/dL [0.88 +/- 0.20 mmol/L] vs 35 +/- 7 mg/dL [0.91 +/- 0.19 mmol/L]). Between 7 and 13 months of age, the serum cholesterol concentration in infants in the intervention group was unchanged, apoB concentration increased slightly, and apoA1 concentration decreased. In the control infants, serum cholesterol concentration increased 9 +/- 25 mg/dL (0.24 +/- 0.65 mmol/L), apoB concentration increased markedly, and apoA1 concentration was stable. Changes in serum lipid and apo concentrations that resulted from the dietary intervention were independent of the apoE phenotype.
The apoE phenotype influenced serum cholesterol concentration markedly by 7 months of age. Between the ages of 7 and 13 months, a reduced saturated fat and cholesterol diet effectively prevented the age-associated increases in serum cholesterol and non-high-density cholesterol concentrations that were obvious in the control infants. The effects of the diet occurred in the infants independently of the apoE phenotype.
遗传性载脂蛋白E(apoE)表型可能决定饮食预防动脉粥样硬化的效果。本研究在一项针对婴儿的为期6个月的低饱和脂肪、低胆固醇饮食前瞻性随机试验中,分析了apoE表型对血清脂质浓度变化的影响。
1062名健康婴儿在7个月大时被随机分为干预组和对照组。当孩子7、8和10个月大时,对干预组家庭进行咨询。饮食目标是孩子自由摄入能量,脂肪占能量的30%至35%,胆固醇摄入量低于200mg/d,饱和脂肪酸、单不饱和脂肪酸和多不饱和脂肪酸的比例为1:1:1。对照组家庭食用无限制饮食。测定了846名婴儿的apoE表型;在7个月和13个月大时测量血清脂质和脂蛋白浓度;并在8个月和13个月大时使用3天食物记录分析营养摄入情况。
在7个月大时,apoE4阳性婴儿(E2/E4、E3/E4和纯合子E4)的血清胆固醇浓度高于apoE4阴性婴儿(159±31mg/dL[4.10±0.81mmol/L]对150±29mg/dL[3.89±0.74mmol/L])。apoE4阳性婴儿的高密度脂蛋白胆固醇浓度略低于apoE4阴性婴儿(34±8mg/dL[0.88±0.20mmol/L]对35±7mg/dL[0.91±0.19mmol/L])。在7至13个月大期间,干预组婴儿的血清胆固醇浓度未发生变化,apoB浓度略有升高,apoA1浓度降低。在对照组婴儿中,血清胆固醇浓度升高了9±25mg/dL(0.24±0.65mmol/L),apoB浓度显著升高,apoA1浓度稳定。饮食干预导致的血清脂质和载脂蛋白浓度变化与apoE表型无关。
apoE表型在7个月大时对血清胆固醇浓度有显著影响。在7至13个月大之间,低饱和脂肪和低胆固醇饮食有效地预防了对照组婴儿中明显的与年龄相关的血清胆固醇和非高密度胆固醇浓度升高。饮食的效果在婴儿中出现,与apoE表型无关。