Department of Bioinformatics, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, ul. Pawinskiego 5A, Warsaw, 02-106, Poland.
Department of Immunology, Transplantology, and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.
BMC Pediatr. 2024 Apr 19;24(1):259. doi: 10.1186/s12887-024-04712-3.
Filiano and Kinney proposed a triple-risk model for the sudden infant death syndrome (SIDS) that involves the intersection of three risks: (1) a vulnerable infant, (2) a critical developmental period in homeostatic control, and (3) an exogenous stressor(s). The primary evidence for the role of a critical developmental period in SIDS etiology is the peak of cases around the third month of life. Independently, several studies pointed to correlation between gestational age and age at death in SIDS, but used that to assess the SIDS risk for preterm infants, ignoring further ramifications.
We did a detailed analysis of CDC data spanning over two decades (1983-2011). We focused not only on the correlation between two age variables (gestational and age at death), but also on the possibility of misdiagnosis. Also, we attempted to account for potential biases in the data induced by the ICD-9/ICD-190 transition or the "Back to Sleep" campaign.
The peak of deaths in the third month of life, that was the main argument for the role of the critical development period, wasn't unique to SIDS. However, we confirmed an almost linear and negative correlation between gestational age and the week of death due to SIDS. This pattern (slope of correlation < 0 and significance of correlation p < 0.05) is characteristic of SIDS among all diseases analyzed in the study.
We interpret the results as the evidence of the role of the critical development period in SIDS etiology. Possibly more attention in the future research should be put to theories that are based on homeostatic control.
菲利亚诺和金尼提出了婴儿猝死综合征(SIDS)的三重风险模型,该模型涉及三个风险的交集:(1)脆弱的婴儿,(2)体内平衡控制的关键发育阶段,以及(3)外部应激源。关键发育阶段在 SIDS 病因学中的作用的主要证据是第三个月左右病例的高峰。独立地,有几项研究指出了 SIDS 中胎龄和死亡年龄之间的相关性,但将其用于评估早产儿的 SIDS 风险,而忽略了进一步的后果。
我们对 CDC 数据进行了二十多年(1983-2011 年)的详细分析。我们不仅关注两个年龄变量(胎龄和死亡年龄)之间的相关性,而且还关注误诊的可能性。此外,我们试图解释由 ICD-9/ICD-10 转换或“回到睡眠”运动引起的潜在数据偏差。
第三个月的死亡高峰,这是关键发育阶段作用的主要论点,并非 SIDS 所独有。然而,我们确认了由于 SIDS 导致的胎龄和死亡周之间几乎线性和负相关。这种模式(相关性斜率<0,相关性的显著性 p<0.05)是研究中分析的所有疾病中 SIDS 的特征。
我们将结果解释为关键发育阶段在 SIDS 病因学中作用的证据。未来的研究可能更应该关注基于体内平衡控制的理论。