A prediction nomogram for faltering catch-up growth in full-term small-for-gestational-age infants: a retrospective
Qian Hu1,2, Sufei Yang1,2, Ping Li1,2
1Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China.
Insights
A new nomogram accurately predicts faltering catch-up growth (FCUG) in small-for-gestational-age (SGA) infants. This tool aids early identification of infants at risk for short stature, enabling timely interventions.
Area of Science:
- Pediatric endocrinology
- Growth and development
- Neonatal care
Background:
- Catch-up growth (CUG) in small-for-gestational-age (SGA) infants is crucial for predicting adult stature.
- Faltering CUG (FCUG) before age two is a key concern for SGA infants.
- Early identification of FCUG risk is essential for intervention.
Purpose of the Study:
- To develop and validate a predictive nomogram for FCUG in full-term SGA infants.
- To identify key predictors of FCUG in this population.
- To provide a tool for early risk stratification of SGA infants.
Main Methods:
- Retrospective cohort study of full-term SGA infants (N=1479).
- Development (1996-2019) and temporal validation (2020-2023) cohorts used.
- Multivariable logistic regression identified predictors: sex, birth weight Z-score, birth length Z-score, and target height Z-score.
Main Results:
- FCUG occurred in 23.6% of the development cohort and 20.4% of the validation cohort.
- The nomogram showed good discrimination (AUC=0.810 in development, 0.784 in validation).
- Key predictors identified were male sex, lower birth weight/length Z-scores, and lower target height Z-score.
Conclusions:
- A clinically applicable nomogram for predicting FCUG in SGA infants has been developed and validated.
- The nomogram reliably identifies infants at high risk for failing to achieve catch-up growth.
- This tool supports early risk stratification and targeted interventions for SGA infants.
Background And Objective:
Catch-up growth (CUG) before two years of age in small-for-gestational-age (SGA) infants is a key predictor of adult short stature. We aimed to establish and temporally validate a prediction nomogram for faltering CUG (FCUG) in full-term SGA infants before two years of age.
Methods:
We conducted a retrospective cohort study of full-term SGA infants at West China Second University Hospital, with cohorts defined as: development (January 1996-December 2019) and temporal validation (January 2020-July 2023). Full-term SGA infants, defined by birth weight or length below 10th percentile per INTERGROWTH-21st standards (n = 1,185 in development; n = 294 in validation). FCUG was defined as failure to increase length-for-age Z score by ≥0.67 above birth Z score by 24 months. Sex, birth weight Z, birth length Z and target height Z scores were entered into a multivariable logistic model. Discrimination (AUC, sensitivity, specificity), calibration (Hosmer-Lemeshow, calibration plot), internal (1,000 bootstrap resamples) and temporal (2020-2023 cohort) validations were performed.
Results:
In the development cohort, 280 of 1,185 (23.6%) of SGA infants experienced FCUG before age two, compared with 60 of 294 (20.4%) in the temporal validation cohort. In multivariable logistic regression analyses, male sex, lower birth length Z score, lower birth weight Z score, and lower target height Z score were all significantly associated with FCUG (all p < 0.05). These four predictors were incorporated into a nomogram. In the development cohort, the model demonstrated excellent discrimination (AUC = 0.810, 95% CI: 0.785-0.835) with a sensitivity of 74% and specificity of 74% at the optimal cut-off. Bootstrap validation (1,000 resamples) confirmed a stable AUC of 0.810. When applied to the temporal cohort, the nomogram achieved an AUC of 0.784 (95% CI: 0.730-0.838), with sensitivity of 93% and specificity of 56%.
Conclusions:
We have developed and temporally validated a clinically applicable nomogram that reliably identifies full-term SGA infants at high risk of failing to achieve catch-up growth by age two. With robust discrimination and calibration, this tool can support early risk stratification and guide targeted nutritional or developmental interventions.
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