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心肌梗死后与年龄相关的胰岛素样生长因子-I、-II及胰岛素样生长因子结合蛋白-3的血清水平

Age-related serum levels of insulin-like growth factor-I, -II and IGF-binding protein-3 following myocardial infarction.

作者信息

Reeves I, Abribat T, Laramee P, Jasmin G, Brazeau P

机构信息

Faculties of Nursing, University of Montreal, Quebec, Canada.

出版信息

Growth Horm IGF Res. 2000 Apr;10(2):78-84. doi: 10.1054/ghir.2000.0143.

Abstract

Aging retards the repair process by decreasing hormone secretion from the somatotrophic axis, which plays a major role in tissue reconstruction after injury. The aim of this study was to determine the effect of aging on serum insulin-like growth factor-I (IGF-I), IGF-II and IGF-binding protein-3 (IGFBP-3) levels following myocardial infarction (MI). For four consecutive days, we monitored the variation of serum IGF-I, IGF-II and IGFBP-3 concentrations in 26 patients aged 19-71 years who were diagnosed with MI. Serum IGF-I, IGF-II and IGFBP-3 were measured daily by double antibody radioimmunoassay. Daily serum IGF-I concentrations showed a significant negative correlation with age (r = -0.528, P< 0.001). Total serum IGF-I was significantly (P = 0.002) higher in the younger age group (patients under 50 years) compared to the older group (50 years and over); 206 +/- 16 ng/ml vs 136 +/- 12 ng/ml. During this investigation, younger patients (under 50 years) showed no significant daily variations in IGF-I levels compared to older patients (50 years and over) who presented a significant decline (P = 0.012). Total serum IGF-II in both groups decreased significantly with time. Total serum IGFBP-3 in the younger age group was significantly higher (P = 0.046) than in the older age group (3.42 +/- 0.18 microgram/ml vs 2.95 +/- 0.13 microgram/ml). MI patients in both groups showed significantly lower IGF-I and IGF-II (IGFs) with higher IGFBP-3 compared to age- and sex-adjusted levels of normal adults (controls). The present results confirm that age and cardiac condition affect IGFs and IGFBP-3 levels. We are inclined to believe that older patients with a cardiac condition are less able to maintain their blood IGF-I levels during the recovery period compared to younger patients. Given the biological impact of IGF-I on regeneration, this could explain why older patients take longer to recover and heal poorly in comparison to younger patients.

摘要

衰老通过减少生长激素轴的激素分泌来延缓修复过程,而生长激素轴在损伤后的组织重建中起主要作用。本研究的目的是确定衰老对心肌梗死(MI)后血清胰岛素样生长因子-I(IGF-I)、IGF-II和IGF结合蛋白-3(IGFBP-3)水平的影响。连续四天,我们监测了26例年龄在19 - 71岁、被诊断为MI的患者血清IGF-I、IGF-II和IGFBP-3浓度的变化。每天通过双抗体放射免疫测定法测量血清IGF-I、IGF-II和IGFBP-3。每日血清IGF-I浓度与年龄呈显著负相关(r = -0.528,P < 0.001)。与老年组(50岁及以上)相比,年轻年龄组(50岁以下患者)的血清总IGF-I显著更高(P = 0.002);分别为206±16 ng/ml和136±12 ng/ml。在本研究期间,与老年患者(50岁及以上)相比,年轻患者(50岁以下)的IGF-I水平每日无显著变化,而老年患者的IGF-I水平则显著下降(P = 0.012)。两组患者的血清总IGF-II均随时间显著下降。年轻年龄组的血清总IGFBP-3显著高于老年年龄组(3.42±0.18微克/毫升对2.95±0.13微克/毫升,P = 0.046)。与年龄和性别调整后的正常成年人(对照组)水平相比,两组MI患者的IGF-I和IGF-II(IGFs)显著降低,而IGFBP-3则更高。目前的结果证实年龄和心脏状况会影响IGFs和IGFBP-3水平。我们倾向于认为,与年轻患者相比,患有心脏疾病的老年患者在恢复期维持其血液IGF-I水平的能力较弱。鉴于IGF-I对再生的生物学影响,这可以解释为什么老年患者与年轻患者相比恢复时间更长且愈合较差。

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