Crecimiento

Crecimiento
  • 文章类型: Journal Article
    背景:我们的目的是确定哪些胎儿或新生儿生长曲线可以区分低出生体重新生儿的胎龄(胎龄小,SGA)和性别(体重<10百分位数),并建立可能对监测10岁以下年龄的生长最有用的曲线。
    方法:分析包括在我们医院(2013-2022)管理的每名新生儿(15.122)和在SEN1500数据库(2019-2022)中登记的32周前出生的所有早产儿(6913)。我们认为,在每个孕龄亚组中,有或没有SGA病史的死亡似然比(LR)最高的曲线最有用。理论上,监测生长的最佳曲线是第50百分位数的分位数回归公式中R2较高的曲线。
    结果:在32周前早产的婴儿中,SGA与住院死亡率之间表现出最强关联的生长曲线是共生胎儿曲线和Fenton新生儿曲线。然而,早产儿和新生儿的最佳曲线总体上是Olsen和Intergrowth的曲线。在10岁之前,仅监测人体测量值最有用的曲线是纵向生长曲线,该曲线遵循WHO标准。但是如果从出生到10岁需要一个单一的参考,最好的选择是遵循WHO标准的Fenton曲线.
    结论:共生参考提供了最有区别的胎儿生长曲线。在新生儿临床实践中,最佳参考是Fenton,其次是WHO图表。
    BACKGROUND: Our aim was to determine which foetal or neonatal growth curves discriminate the probability of dying of newborns with low birth weight for their gestational age (small for gestational age, SGA) and sex (weight < 10th percentile) and to establish the curves that are presumably most useful for monitoring growth through age 10 years.
    METHODS: The analysis included every neonate (15 122) managed in our hospital (2013-2022) and all neonates born preterm before 32 weeks (6913) registered in the SEN1500 database (2019-2022). We considered most useful those curves with the highest likelihood ratio (LR) for dying with or without a history of SGA in each subgroup of gestational ages. Theoretically, the optimal curves for monitoring growth would be those with a higher R2 in the quantile regression formulas for the 50th percentile.
    RESULTS: The growth curves exhibiting the strongest association between SGA and hospital mortality are the Intergrowth fetal curves and the Fenton neonatal curves in infants born preterm before 32 weeks. However, the optimal curves for premature babies and neonates overall were those of Olsen and Intergrowth. The most useful curves to monitor anthropometric values alone until age 10 years of age are the longitudinal Intergrowth curves followed by the WHO standards, but if a single reference is desired from birth through age 10 years, the best option is the Fenton curves followed by the WHO standards.
    CONCLUSIONS: The Intergrowth reference provides the most discriminating foetal growth curves. In neonatal clinical practice, the optimal references are the Fenton followed by the WHO charts.
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  • 文章类型: Observational Study
    BACKGROUND: Early detection of suspected neurodevelopmental delay allows for timely diagnosis and appropriate intervention, for which numerous screening tests have been developed. However, most are complex and impractical for health-care workers at the community level. This study aimed to validate the KARVI scale in the neurodevelopment assessment of children under 1 year of age.
    METHODS: We conducted an observational, longitudinal, comparative, inferential, and prospective study. Healthy children without risk factors for developing neurodevelopmental delay from 0 to 12 months of age were evaluated remotely using the Zoom® application. The Child Development Evaluation Test and the KARVI scale were applied once a month for four consecutive months.
    RESULTS: Fifty individuals were analyzed, with a predominance of males in 52%. Adequate percentages for a screening test were obtained in the first evaluation with a sensitivity of 70% (confidence interval [CI] 95% 34.75-93.33) and a specificity of 75% (CI 95% 58.8-87.31), and in the fourth evaluation with a sensitivity of 100% (CI 95% 29.4-100) and a specificity of 78.72% (CI 95% 64.34-89.3), being significant in both evaluations (p = 0.007 and p = 0.001, respectively).
    CONCLUSIONS: The KARVI scale has the elements to be an effective screening test for suspected neurodevelopmental delay, but more extensive studies are needed to obtain more reliable results.
    UNASSIGNED: La identificación temprana de retraso en el neurodesarrollo permite un diagnóstico oportuno y una intervención apropiada. Para ello, se han creado diversas pruebas de tamizaje; sin embargo, la mayoría son complejas y poco prácticas para el personal de la salud a nivel comunitario. El objetivo del estudio fue realizar la validación de la escala KARVI en la valoración del neurodesarrollo en niños menores de un año.
    UNASSIGNED: Se realizó un estudio observacional, longitudinal, comparativo inferencial y prospectivo, en el cual se evaluaron, vía remota mediante la aplicación Zoom®, niños sanos de 0 a 12 meses de edad sin factores de riesgo para desarrollar retraso en el neurodesarrollo. Se aplicaron la prueba EDI (Evaluación del Desarrollo Infantil) y la escala KARVI una vez al mes por cuatro meses consecutivos.
    RESULTS: Se analizaron 50 individuos, con predominio del sexo masculino en el 52%. Se obtuvieron porcentajes adecuados para una prueba de tamizaje tanto en la primera evaluación, con sensibilidad de 70% (IC 95% 34.75-93.33) y especificidad de 75% (IC 95% 58.8-87.31), como en la cuarta, con sensibilidad de 100% (IC 95% 29.4-100) y especificidad de 78.72% (IC 95% 64.34-89.3), con significación estadística en ambas evaluaciones (p = 0.007 y p = 0.001, respectivamente).
    CONCLUSIONS: Se considera que la escala KARVI cuenta con los elementos para considerarla como una prueba de tamizaje efectiva para detectar retraso del neurodesarrollo, sin embargo. Sin requieren estudios más extensos para obtener resultados más confiables.
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  • 文章类型: Journal Article
    目的:ADV7103是一种用于远端肾小管酸中毒(dRTA)的新型缓释治疗方法,含有柠檬酸钾和碳酸氢钾。由于酸中毒可能会影响骨矿物质含量,评价ADV7103对dRTA患者24个月以上骨矿物质密度(BMD)和生长的影响.
    方法:在II/III期试验后,30名患者(24名儿科患者和6名成人)被纳入开放标签延伸研究。BMD,通过密度测定法测量,在基线和24个月时进行评估。在整个研究中评价生长。血浆碳酸氢盐,甲状旁腺激素,25-羟基维生素D,1,25-二羟基维生素D,骨碱性磷酸酶,钙尿症和血尿,也决心。还评估了安全性和治疗依从性。
    结果:使用ADV7103治疗24个月后,平均脊柱BMDz评分与基线相比显着增加(p=0.024)。在成年人中,脊柱和全身密度测定z评分显示与血浆碳酸氢盐水平显着相关(rS=0.82和rS=0.97,p<0.005)。18%和36%的儿科患者的身高和体重z评分增加>0.5个单位,分别。经过治疗,血浆碳酸氢盐浓度和钙尿在不同的访问是正常的69-86%和93-96%的患者,分别。只有9种治疗相关的轻度/中度胃肠道不良事件,在五名患者中报告。
    结论:两年的ADV7103治疗改善了生长并增加了脊柱BMD。这些结果表明,通过ADV7103治疗控制酸中毒可以改善骨骼参数。
    ADV7103 is a new prolonged-release treatment for distal renal tubular acidosis (dRTA), containing potassium citrate and potassium bicarbonate. Since acidosis may affect bone mineral contents, the effects of ADV7103 on bone mineral density (BMD) and growth in patients with dRTA over 24 months were evaluated.
    Thirty patients (24 paediatric patients and 6 adults) were included in an open-label extension study after a phase II/III trial. BMD, measured by densitometry, was assessed at baseline and at 24 months. Growth was evaluated throughout the study. Plasma bicarbonate, parathyroid hormone, 25-hydroxy vitamin D, 1,25-dihydroxy vitamin D, bone alkaline phosphatase, calciuria and citraturia, were also determined. Safety and treatment compliance were evaluated as well.
    After 24 months of treatment with ADV7103, mean spine BMD z-score values significantly increased as compared with baseline (p=0.024). In adults, spine and whole-body densitometry z-scores showed a significant correlation with plasma bicarbonate levels (rS=0.82 and rS=0.97, respectively, p<0.005). There was an increase>0.5 units in z-scores for height and weight in 18% and 36% of the paediatric patients, respectively. With treatment, plasma bicarbonate concentration and calciuria at the different visits were normal in 69-86% and 93-96% patients, respectively. Only nine treatment-related gastrointestinal AEs of mild/moderate severity, were reported in five patients.
    Two years of ADV7103 treatment improved growth and increased spine BMD. These results suggest that control of acidosis by ADV7103 treatment improves bone parameters.
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  • 文章类型: Journal Article
    目的:原发性肾小管病很少见,通常在小儿年龄出现。基因诊断和治疗的最新进展改变了其自然史。本研究提供了在儿科肾病科诊断出的一系列原发性肾小管疾病的临床谱,并提供了有关生长的长期随访数据,估计肾小球滤过(eGFR)和并发并发症。
    方法:对53例原发性肾小管病变并确定遗传缺陷的患者进行观察性研究:Gitelman综合征(36%),远端肾小管酸中毒(15%),胱氨酸尿症(11%),X-连锁低磷酸盐血症病(7%),凹处综合征Lowe(7%),胱氨酸病(6%),其他肾小管病变1-2例。人口统计,在诊断时收集分析和临床数据,在进化过程中和研究时。
    结果:诊断时的年龄(中位数和四分位数范围)为5.08岁(1.33-8.50)。最常见的表现是与并发过程相关的代谢失代偿(40%)和身材矮小(38%)。诊断时的身高(平均±SD)为-1.39±1.49,随访18.92(6.25-24.33)年后为1.07±1.54。16(32%)的eGFR<90ml/min/1.73m2。3例患者需要进行肾脏置换。11例患者代谢失代偿需要住院治疗,9肾绞痛和/或肾结石和10个精神问题。8例远端肾小管酸中毒患者中有6例发展为感音神经性耳聋。
    结论:原发性肾小管病变是一组异质性疾病,可导致生长障碍,治疗在很大程度上是可逆的,eGFR降低和显著的肾外并发症衍生或相关的风险。
    OBJECTIVE: Primary tubulopathies are rare and usually present at pediatric age. Recent advances in genetic diagnosis and treatment have changed its natural history. This study provides the clinical spectrum of a series of primary tubulopathies diagnosed in a Pediatric Nephrology Unit and to offer long-term follow-up data regarding growth, estimated glomerular filtration (eGFR) and intercurrent complications.
    METHODS: Observational study in 53 patients with primary tubulopathies and identified genetic defect: Gitelman syndrome (36%), distal renal tubular acidosis (15%), cystinuria (11%), X-linked hypophosphatemic rickets (7%), Dent-syndrome Lowe (7%), cystinosis (6%), and 1-2 cases of other tubulopathies. Demographic, analytical and clinical data were collected at diagnosis, during evolution and at the time of the study.
    RESULTS: The age (median and interquartile range) at diagnosis was 5.08 years (1.33-8.50). The most frequent presentation manifestations were metabolic decompensations associated with intercurrent processes (40%) and short stature (38%). Height (mean ± SD) was -1.39 ± 1.49 at diagnosis and 1.07 ± 1.54 after a follow-up of 18.92 (6.25-24.33) years. Sixteen (32%) developed an eGFR <90 ml/min/1.73 m2. Three patients required replacement renal replacement. Eleven patients had metabolic decompensations that required hospitalization, 9 renal colic and/or kidney stones and 10 mental problems. Six of 8 patients with distal renal tubular acidosis developed sensorineural deafness.
    CONCLUSIONS: Primary tubulopathies are a heterogeneous group of diseases that cause growth impairment, largely reversible with treatment, risk of eGFR reduction and significant extrarenal complications derived or associated.
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  • 文章类型: Journal Article
    目的:生酮饮食疗法(KDT)产生抗惊厥和神经保护作用,减少癫痫发作,改善癫痫患者的认知状态。我们的目的是评估KDT对难治性癫痫儿童的影响(有效性,副作用,对营养状况和生长的影响)。
    方法:在西班牙一家三级医院(2000年1月至2018年12月)进行了一项回顾性和前瞻性观察性描述性研究。160例小儿癫痫患者接受了KDT治疗(男性82例;平均年龄5岁9个月)。癫痫发作,抗癫痫药物,人体测量,副作用,和实验室评估在基线和KDT发病后3,6,12和24个月进行监测.
    结果:在这些时间间隔中,无癫痫患者分别为:13.7、12.5、14.4和10.6%,分别,41.9、37.5、28.7和16.2%的癫痫发作减少≥50%。副作用很频繁,尤其是消化系统疾病,高钙尿症,低血糖,肝功能异常和血脂异常。前白蛋白,视黄醇结合蛋白,维生素A和镁显著下降。身高受到影响,尤其是2岁以下的儿童。
    结论:KDT治疗儿童难治性癫痫有效。然而,不良反应频繁,它可能会影响营养状况和生长。
    OBJECTIVE: Ketogenic dietary therapies (KDT) produce anticonvulsant and neuroprotective effects, reduce seizures and improve the cognitive state in patients with epilepsy. Our purpose was to evaluate the effects of KDT in children with refractory epilepsy (effectiveness, side effects, impact on nutritional status and growth).
    METHODS: A retrospective and prospective observational descriptive study was conducted in a Spanish tertiary hospital (January 2000 to December 2018). One hundred sixty pediatric patients with epilepsy were treated with KDT (82 males; mean age 5 years 9 months). Seizures, anti-epileptic drugs, anthropometric measures, side effects, and laboratory assessment were monitored baseline and at 3, 6, 12 and 24 months after the onset of KDT.
    RESULTS: In these time intervals, the seizure-free patients were: 13.7, 12.5, 14.4 and 10.6%, respectively, and a reduction of seizures ≥ 50% was achieved in 41.9, 37.5, 28.7 and 16.2%. Side effects were frequent, especially digestive disorders, hypercalciuria, hypoglycemia, hepatic dysfunction and dyslipidemia. Prealbumin, retinol binding protein, vitamin A and magnesium decreased significantly. Height was affected, especially in children below 2 years.
    CONCLUSIONS: KDT are effective for refractory epilepsy in children. However, adverse effects are frequent, and it may affect nutritional status and growth.
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  • 文章类型: Journal Article
    Growth and development reflect the child\'s health condition. Currently, child care is supported in daycare centers. In this context, this article aimed to identify the differences in growth and psychomotor development in children according to their attendance at daycare centers.
    We conducted an analytical cross-sectional study in children aged 25 to 48 months. Two groups were identified: 68 children attended daycare, and 68 children did not attend daycare. Growth was assessed with weight-for-height curves, and psychomotor development was evaluated with the child developmental assessment instrument (psychosocial, language, psychomotor, and cognitive area). The X2 test was used for statistical analysis.
    The percentage of daycare children with ideal weight was higher than those not attending in daycare (p = 0.035). Psychomotor development was significantly higher in daycare children: in the psychosocial (p = 0.000), language (p = 0.000), motor (p = 0.000), and cognitive development (p = 0.000) areas.
    The psychomotor development of children attending daycare centers is superior to that of children not in daycare centers.
    La salud del niño se puede evaluar a partir de su crecimiento y desarrollo. En la sociedad actual, el cuidado de los hijos se comparte con las guarderías infantiles. En este contexto, el objetivo del artículo fue identificar las diferencias de crecimiento y desarrollo psicomotor en niños de acuerdo con su asistencia a las guarderías.
    Se llevó a cabo un estudio transversal analítico en niños de 25 a 48 meses de edad. Se identificaron dos grupos: 68 niños atendidos en guarderías y 68 niños no atendidos en guarderías. El crecimiento se evaluó con las curvas de peso para la talla y el desarrollo psicomotor, con el instrumento de evaluación del desarrollo del niño (área psicosocial, lenguaje, psicomotriz, y cognitiva). Se utilizó la prueba de X2 para el análisis estadístico.
    El porcentaje de niños de guardería con peso ideal es superior al de los no atendidos en guardería (p = 0.035). El desarrollo psicomotor es significativamente mayor en los niños de guardería: en el área psicosocial (p = 0.000), en lenguaje (p = 0.000), en el área motriz (p = 0.000) y en desarrollo cognitivo (p = 0.000).
    El desarrollo psicomotor de los niños atendidos en guardería es superior al de los niños no atendidos en guardería.
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  • 文章类型: Journal Article
    OBJECTIVE: To validate regression equations that predict the state of maturity (MS) to evaluate the physical growth and body fatness of Chilean children and adolescents.
    METHODS: A transversal study was carried out in 8094 school children between 6.0 and 18.9 years old. Weight, standing height, sitting height, and waist circumference (WC) were evaluated. Peak growth rate (PVC) was estimated by the mathematical model 1 of Preece-Baines (MPB). Mirwald\'s equations (based on age, weight, standing height, sitting height, and leg length) and Moore\'s equations (based on age, weight, and standing height) were used to estimate MS. The body mass index (BMI) was calculated.
    RESULTS: The BMP showed that the PVC in men was 10.33 ± 0.29 years and in women was 12.81 ± 0.27 years. Using Mirwald\'s equation, men reached MS at 14.09 ± 0.8 APVC and women at 11.6 ± 0.9 APVC, while using Moore\'s equation, men reached 13.7 ± 0.6 APVC and women at 12.1 ± 0.6 APVC. There were significant differences between MPB with Mirwald, MPB with Morre, and between Mirwald and Moore (p < 0.001). Explanation values by MS category were Mirwald\'s equation [men (early R2 = 0.81, mean R2 = 0.69 and late R2 = 0.09) and women (early R2 = 0.83, mean R2 = 0.83 and late R2 = 0.77)], Moore\'s equation [men (early R2 = 0.93, mean R2 = 0.70 and late R2 = 0.79) and women (early R2 = 0.89, mean R2 = 0.89 and late R2 = 0.83)]. Percentiles were created for weight, height, CC and BMI.
    CONCLUSIONS: It was verified that Moore\'s and Mirwald\'s equations differ with the mathematical model MPB in both sexes. However, Moore\'s equation could be useful for the evaluation of MS in Chilean children and adolescents.
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  • 文章类型: Journal Article
    El zinc (Zn) es un oligoelemento esencial para muchas funciones biológicas, que incluyen desde la mineralización ósea hasta la transcripción genómica. El déficit en la ingesta de Zn produce alteraciones que en conjunto se han denominado síndrome de deficiencia de Zn. La ingesta diaria recomendada presenta un rango de 7.5 a 15 mg/día para hombres adultos y de 5.5 a 12 mg/día para mujeres adultas. En México, el déficit de Zn es un problema de salud pública, pues afecta a cerca de un cuarto de la población pediátrica nacional. Este documento presenta al lector una mirada global y regional sobre el problema que se aborda, y destaca la necesidad de generar líneas de investigación que aporten mayor información sobre el impacto de este micronutriente en la población mexicana.
    Zinc (Zn) is an essential trace element for many biological functions including bone mineralization and genomic ­transcription, among others. The set of clinical manifestations deriving from the deficiency of Zn intake are known as Zn deficit syndrome. Zn recommended dietary allowances ranges from 7.5 to 15 mg/day in adult man, and from 5.5 to 12 mg/day in adult females. In Mexico, the deficit of Zn is a public health problem affecting nearly a quarter of pediatric population. This document presents a global and regional overview of this problem, highlighting the need of further research related to the importance of this micronutrient in Mexican population.
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  • 文章类型: English Abstract
    目的:生酮饮食疗法(KDT)产生抗惊厥和神经保护作用,减少癫痫发作,改善癫痫患者的认知状态。我们的目的是评估KDT对难治性癫痫儿童的影响(有效性,副作用,对营养状况和生长的影响)。
    方法:在西班牙一家三级医院(2000年1月至2018年12月)进行了一项回顾性和前瞻性观察性描述性研究。160例小儿癫痫患者接受了KDT治疗(男性82例;平均年龄5岁9个月)。癫痫发作,抗癫痫药物,人体测量,副作用,和实验室评估在基线和KDT发病后3,6,12和24个月进行监测.
    结果:在这些时间间隔中,无癫痫患者分别为:13.7、12.5、14.4和10.6%,分别,41.9、37.5、28.7和16.2%的癫痫发作减少≥50%。副作用很频繁,尤其是消化系统疾病,高钙尿症,低血糖,肝功能异常和血脂异常。前白蛋白,视黄醇结合蛋白,维生素A和镁显著下降。身高受到影响,尤其是2岁以下的儿童。
    结论:KDT治疗儿童难治性癫痫有效。然而,不良反应频繁,它可能会影响营养状况和生长。
    OBJECTIVE: Ketogenic dietary therapies (KDT) produce anticonvulsant and neuroprotective effects, reduce seizures and improve the cognitive state in patients with epilepsy. Our purpose was to evaluate the effects of KDT in children with refractory epilepsy (effectiveness, side effects, impact on nutritional status and growth).
    METHODS: A retrospective and prospective observational descriptive study was conducted in a Spanish tertiary hospital (January 2000 to December 2018). One hundred sixty pediatric patients with epilepsy were treated with KDT (82 males; mean age 5 years 9 months). Seizures, anti-epileptic drugs, anthropometric measures, side effects, and laboratory assessment were monitored baseline and at 3, 6, 12 and 24 months after the onset of KDT.
    RESULTS: In these time intervals, the seizure-free patients were: 13.7, 12.5, 14.4 and 10.6%, respectively, and a reduction of seizures≥50% was achieved in 41.9, 37.5, 28.7 and 16.2%. Side effects were frequent, especially digestive disorders, hypercalciuria, hypoglycemia, hepatic dysfunction and dyslipidemia. Prealbumin, retinol binding protein, vitamin A and magnesium decreased significantly. Height was affected, especially in children below 2 years.
    CONCLUSIONS: KDT are effective for refractory epilepsy in children. However, adverse effects are frequent, and it may affect nutritional status and growth.
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  • 文章类型: Journal Article
    目的:验证预测成熟状态(MS)的回归方程,以评估智利儿童和青少年的身体发育和身体脂肪。
    方法:对8,094名6.0至18.9岁的学童进行了横向研究。重量,站立高度,坐姿高度,和腰围(WC)进行了评估。通过Preece-Baines(MPB)的数学模型1估算峰值生长速率(PVC)。米尔沃尔德方程(基于年龄,体重,站立高度,坐姿高度,和腿长)和摩尔方程(基于年龄,体重,和站立高度)用于估计MS。计算体重指数(BMI)。
    结果:BMP显示,男性的PVC为10.33±0.29年,女性为12.81±0.27年。使用Mirwald的方程,男性在14.09±0.8APVC时达到MS,女性在11.6±0.9APVC时达到MS,在使用摩尔方程时,男性达到13.7±0.6APVC,女性达到12.1±0.6APVC。MPB与Mirwald之间存在显着差异,与Morre的MPB,在Mirwald和Moore之间(p<0.001)。MS类别的解释值是Mirwald\'s方程[男性(早期R2=0.81,平均R2=0.69和晚期R2=0.09)和女性(早期R2=0.83,平均R2=0.83和晚期R2=0.77)]。摩尔方程[男性(早期R2=0.93,平均R2=0.70和晚期R2=0.79)和女性(早期R2=0.89,平均R2=0.89和晚期R2=0.83)]。百分位数是为体重创造的,高度,CC和BMI。
    结论:验证了Moore\和Mirwald\方程在两性中与数学模型MPB不同。然而,摩尔方程可用于智利儿童和青少年MS的评估。
    OBJECTIVE: To validate regression equations that predict the state of maturity (MS) to evaluate the physical growth and body fatness of Chilean children and adolescents.
    METHODS: A transversal study was carried out in 8,094 school children between 6.0 and 18.9 years old. Weight, standing height, sitting height, and waist circumference (WC) were evaluated. Peak growth rate (PVC) was estimated by the mathematical model 1 of Preece-Baines (MPB). Mirwald\'s equations (based on age, weight, standing height, sitting height, and leg length) and Moore\'s equations (based on age, weight, and standing height) were used to estimate MS. The body mass index (BMI) was calculated.
    RESULTS: The BMP showed that the PVC in men was 10.33±0.29 years and in women was 12.81±0.27 years. Using Mirwald\'s equation, men reached MS at 14.09±0.8APVC and women at 11.6±0.9APVC, while using Moore\'s equation, men reached 13.7±0.6APVC and women at 12.1±0.6APVC. There were significant differences between MPB with Mirwald, MPB with Morre, and between Mirwald and Moore (p<0.001). Explanation values by MS category were Mirwald\'s equation [men (early R2=0.81, mean R2=0.69 and late R2=0.09) and women (early R2=0.83, mean R2=0.83 and late R2=0.77)], Moore\'s equation [men (early R2=0.93, mean R2=0.70 and late R2=0.79) and women (early R2=0.89, mean R2=0.89 and late R2=0.83)]. Percentiles were created for weight, height, CC and BMI.
    CONCLUSIONS: It was verified that Moore\'s and Mirwald\'s equations differ with the mathematical model MPB in both sexes. However, Moore\'s equation could be useful for the evaluation of MS in Chilean children and adolescents.
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