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Table 5 Association of infectious disease morbidity from 6 to 18 mo with developmental delay at 18 mo

From: The association of malaria morbidity with linear growth, hemoglobin, iron status, and development in young Malawian children: a prospective cohort study

Independent Variables

Developmental delaya

(N = 2016)

Fine motor delay

Gross motor delay

Language delay

PSED delay

Risk ratiob

P-value

Risk ratiob

P-value

Risk ratiob

P-value

Risk ratiob

P-value

(95% CI)

(95% CI)

(95% CI)

(95% CI)

Incidencec of ‘presumed’ malaria

1.03 (0.96 to 1.09)

0.435

1.04 (1.00 to 1.09)

0.059

0.99 (0.94 to 1.06)

0.926

0.95 (0.88 to 1.02)

0.145

> 1 malaria episodes (vs no malaria episode)

0.96 (0.78 to 1.19)

0.723

1.06 (0.89 to 1.27)

0.508

1.00 (0.82 to 1.23)

0.971

0.82 (0.66 to 1.03)

0.094

Incidencec of diarrhea

1.01 (1.00 to 1.02)

0.011

1.01 (1.00 to 1.02)

< 0.001

1.00 (0.99 to 1.01)

0.129

1.00 (0.99 to 1.01)

0.953

Incidencec of ARI

0.99 (0.97 to 1.01)

0.367

0.99 (0.98 to 1.01)

0.445

0.99 (0.97 to 1.01)

0.338

1.02 (1.00 to 1.04)

0.025

Other predictorsd

 Female sex (vs. male)

1.13 (0.91 to 1.41)

0.253

1.50 (1.22 to 1.85)

< 0.001

0.92 (0.74 to 1.14)

0.438

0.77 (0.61 to 0.96)

0.023

 LAZ at age 6 mo

0.90 (0.81 to 1.00)

0.059

0.82 (0.73 to 0.91)

< 0.001

0.87 (0.78 to 0.97)

0.014

0.97 (0.86 to 1.08)

0.533

 WLZ at age 6 mo

0.84 (0.76 to 0.93)

0.001

0.97 (0.88 to 1.07)

0.517

0.97 (0.88 to 1.07)

0.542

0.92 (0.83 to 1.03)

0.145

 HFIA score

0.98 (0.96 to 0.99)

0.034

0.99 (0.98 to 1.01)

0.702

1.01 (0.99 to 1.03)

0.091

1.02 (0.99 to 1.04)

0.075

 Child’s mood

0.38 (0.29 to 0.49)

< 0.001

0.67 (0.55 to 0.83)

< 0.001

1.08 (0.89 to 1.33)

0.435

0.78 (0.63 to 0.97)

0.023

 Activity level

0.92 (0.67 to 1.25)

0.587

0.67 (0.51 to 0.87)

0.003

0.91 (0.65 to 1.29)

0.610

1.57 (1.12 to 2.21)

0.009

  1. ARI acute respiratory infection, CI confidence interval, HFIA household food insecurity access, LAZ length for age z-score, PSED Profile of Social and Emotional Development
  2. aDefined as the bottom 25% of our sample
  3. bObtained by modified poisson regression (with a robust variance estimator)
  4. cTotal episodes/child years at risk
  5. dOnly predictors that showed statistical significance in any of the multivariate models are presented. Other variables entered in the regression, but not significant in any model, were: hemoglobin concentration; iron status; maternal education; interaction with the assessor during the Kilifi Developmental Inventory (KDI) assessment; and whether the child received an intervention (lipid-based nutrient supplements) during the study period