Identification of Putative Biomarkers in Cerebral Palsy: A Meta-Analysis and Meta-Regression

被引:0
|
作者
Suresh, Vinay [1 ]
Gupta, Shiva [1 ]
Khulbe, Yashita [1 ]
Shamim, Muhammad Aaqib [2 ]
Jain, Vaibhav [3 ]
Jayan, Malavika [4 ]
Waleed, Madeeha Subhan [5 ]
Joe, Neha [6 ]
Sanker, Vivek [7 ]
Gandhi, Aravind P. [8 ]
Alam, Areesha [9 ]
Malhotra, Hardeep Singh [10 ,11 ]
Garg, Ravindra K. [12 ]
Gulati, Sheffali [13 ]
Roy, Priyanka [14 ]
Bardhan, Mainak [15 ,16 ]
机构
[1] King Georges Med Univ, Lucknow, India
[2] All India Inst Med Sci Jodhpur, Dept Pharmacol, Jodhpur, India
[3] Davao Med Sch Fdn, Davao, Philippines
[4] Bangalore Med Coll & Res Inst, Bangalore, Karnataka, India
[5] Lower Bucks Hosp, Bristol, PA USA
[6] St Johns Med Coll, Bengaluru, Karnataka, India
[7] Trivandrum Med Coll, Dept Neurosurg, Thiruvananthapuram, Kerala, India
[8] ES Med Coll & Hosp, Dept Community Med, Hyderabad, India
[9] King Georges Med Univ, Dept Pediat, Lucknow, India
[10] King Georges Med Univ, Dept Neurol, Lucknow, India
[11] King Georges Med Univ, Res Cell & Dev, Lucknow, India
[12] King Georges Med Univ, Head Dept, Dept Neurol, Lucknow, India
[13] All India Inst Med Sci, Dept Pediat, Child Neurol Div, New Delhi, India
[14] Directorate Factories, Dept Labour, , Govt West Bengal, Kolkata, India
[15] Miami Canc Inst, Neuromed Oncol, Baptist Hlth South Florida, 8900 N. Kendall Dr, Miami, FL 33176 USA
[16] Natl Inst Mental Hlth & Neurosci NIMHANS, Dept Neurol, Bengaluru, India
关键词
Cerebral palsy; Biomarker; Beta-HCG; Nuchal translucency; PAPP-A; HUMAN CHORIONIC-GONADOTROPIN; INCREASED NUCHAL TRANSLUCENCY; ADVERSE PREGNANCY OUTCOMES; FOR-GESTATIONAL-AGE; EARLY FETAL-GROWTH; PAPP-A LEVELS; FREE BETA-HCG; PLASMA-PROTEIN; 1ST TRIMESTER; RISK;
D O I
10.1016/j.pediatrneurol.2024.07.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Cerebral palsy (CP) is a neurological disorder that impairs motor abilities. Identifying maternal biomarker derangements can facilitate further evaluation for early diagnosis, potentially leading to improved clinical outcomes. This study investigates the association between maternal biomarker derangements and CP development during the antenatal period. Methods: A systematic search was conducted in MEDLINE, EMBASE, and Cochrane databases, following MOOSE guidelines. Data on participants exceeding biomarker thresholds (95th and 5th percentiles) were extracted for combined odds ratio estimation. Geometric mean differences, reported as multiples of the median (MoMs), were used to analyze changes in marker levels. Trimesterwise subgroup analysis and metaregression assessed the impact of variables on outcomes. Results: Five observational studies (1552 cases, 484,985 controls) revealed lower maternal pregnancyassociated plasma protein A levels were associated with CP (pooled odds ratio [OR] = 1.60, 95% confidence interval [CI] = 1.22 to 2.09; I = 0%), with a -0.04 MoM geometric mean difference. Lower maternal beta-human chorionic gonadotropin (HCG) levels in first and second trimesters indicated a pooled OR = 1.18 (95% CI = 0.85 to 1.63; I = 57%). Sensitivity analysis showed an OR =1.40 (95% CI =1.08 to 1.82; I = 0%), with a -0.07 MoM geometric mean difference. Metaregression identified primigravida status as negatively influencing beta-HCG levels. Elevated nuchal translucency values and CP presented a pooled OR = 1.06 (95% CI = 0.77 to 1.44; I = 0%). Conclusion: Lower maternal pregnancy-associated plasma protein A levels during the first trimester and lower beta-HCG levels in the first and second trimesters are associated with CP development in children. Future research should validate the predictive utility of these biomarkers and explore novel ones through large-scale cohort studies. (c) 2024 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页码:43 / 54
页数:12
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