Growth
•Growth is a continuum that involves changes in body size and form, changes in physiologic function, and biologic maturation •A corresponding increase in cell size and number; no true normal, rather an “average” (50th percentile) plus or minus two standard deviations
Body Mass Index (BMI) = weight (kg) / height (m)2 For children, BMI is age and gender specific; so BMI-for- age is the measure used in growth chart
Anthropometric Index Indicator
Percentile Cut-off Value
BMI-for-Age
Nutritional Status
≥ 95th Overweight Weight-for-Length
BMI-for-Age
≥ 85th and < 95th
BMI-for-Age Weight-for-Length
< 5th
Underweight
Stature/Length-for-Age
< 5th
Short Stature
Head Circumference- for-Age
< 5th and > 95th
> 95th
At Risk of Overweight
Developmental Problems
35 30 25
5th
20 15 10
95th
30
50th
BMI
Weight (kg)
35
95th
25
50th
20
5th
15
5 0 80 90 100 110 120 130 Stature (cm)
10 24
72
120 168 216
Age (months)
For Children, BMI Changes with Age BMI
BMI
Example: 95th Percentile Tracking
Boys: 2 to 20 years
BMI
BMI
Age
BMI
2 yrs 4 yrs 9 yrs 13 yrs
19.3 17.8 21.0 25.1
Can you see risk? • •
This boy is 3 years, 3 weeks old. Is his BMI-for-age - >85th to <95th percentile: overweight?
at risk for
Plotted BMI-for-Age BMI
BMI
Boys: 2 to 20 years
Measurements:
Age=3 y 3 wks Height=100.8 cm (39.7 in) Weight=18.6 kg (41 lb) BMI=18.3 BMI-for-age= >95th percentile overweight
BMI
BMI
Can you see risk? • •
This girl is 4 years, 4 weeks old. Is her BMI-for-age - >85th to <95th percentile: overweight?
at risk for
Plotted BMI-for-Age Measurements: BMI
BMI
Girls: 2 to 20 years
Age= 4 y 4 wks Height=106.4 cm (41.9 in) Weight=15.7 kg (34.5 lb) BMI=13.9 BMI-for-age= 10th percentile Normal
BMI
BMI
Can you see risk? • •
This girl is 4 years old. Is her BMI-for-age - >85th to <95th percentile: overweight?
at risk for
Plotted BMI-for-Age BMI
BMI
Measurements:
Age=4 y
Height=99.2 cm (39.2 in)
Girls: 2 to 20 years
Weight=17.55 kg (38.6 lb) BMI=17.8 BMI-for-age= between 90th –95th percentile At risk for overweight BMI
BMI
Summary of Using BMI-for-Age • BMI-for-age is the recommended method for screening overweight and underweight • For children, BMI is age and gender specific; for adults there are fixed cut points • Accurate and periodic measurements are important elements of any anthropometric screening
Obtain accurate weight and height measurements Select the appropriate growth chart Record the data Calculate BMI Plot measurements Interpret plotted measurements
Short stature Measurement that falls below the 3rd – 5th percentile for height is the short stature Risk factors/etiology: •Pathologic (postnatal onset) •Constitutional growth delay
•Familial short stature •Prenatal onset short stature (IUGR)
Presentation: Pathologic : Starts with the patient in the normal range for height Over time, starts falling off the height curve, crossing percentiles Constitutional: Starts with the patient in the normal range for height Over time, normal final adult height is reached , but the growth spurt and puberty are delayed
Causes of short stature A. Genetic-familial short stature B. Constitutional growth delay C. Endocrine disturbances 1. Growth hormone deficiency 2. Hypothyroidism 3. Excess cortisol—Cushing disease and Cushing syndrome (including iatrogenic causes) 4. Precocious puberty 5. Diabetes mellitus (poorly controlled) 6. Pseudohypoparathyroidism 7. Rickets
Causes of short stature (contd…) D. Intrauterine growth restriction 1. Intrinsic fetal abnormalities—chromosomal disorders 2. Syndromes (eg, Noonan ) 3. Congenital infections 4. Placental abnormalities 5. Maternal abnormalities a. Hypertension/toxemia b. Drug use c. Malnutrition
Causes of short stature (contd…) E. Inborn errors of metabolism 1. Mucopolysaccharidosis 2. Other storage diseases F. Intrinsic diseases of bone 1. Defects of growth of tubular bones or spine (eg, achondroplasia) 2. Disorganized development of cartilage and fibrous components of the skeleton (eg, multiple cartilaginous exostoses, fibrous dysplasia with skin pigmentation)
Causes of short stature (contd…) G. Short stature associated with chromosomal defects 1. Autosomal (eg, Down syndrome, Prader-Willi syndrome) 2. Sex chromosomal (eg, Turner syndrome-XO) H. Chronic systemic diseases, congenital defects, and cancers (eg, chronic infection and infestation, IBD, hepatic disease, CVS disease, hematologic disease, CNS disease, pulmonary disease, renal disease, malnutrition, cancers, collagen vascular disease) I. Psychosocial short stature (deprivation dwarfism)
Familial: Stays parallel to the growth curve Strong family history of short stature Prenatal short stature: Parallel to the growth curve but much more marked
Diagnostic tests •Growth chart •Physical exam •Karyotype (Turner syndrome) •X-ray (left hand and wrist ) for bone age Treatment: •Correction of the underlying disease state •Growth hormone in selected cases D/D: Work-up for short stature
•Familial: A normal variant, •Exogenous obesity •Endocrine: growth hormone excess (gigantism, acromegaly) •Androgen excess (tall as children but short as adults) •Hyperthyroidism •Genetic syndromes metabolic disorders: homocystinuria, cerebral gigantism , BeckwithWiedemann, Weaver-Smith, and Klinefelter syndrome
A. Constitutional (familial) B. Exogenous obesity C. Endocrine causes 1. Growth hormone excess (pituitary gigantism) 2. Precocious puberty 3. Hypogonadism D. Nonendocrine causes 1. Klinefelter syndrome 2. XYY males 3. Marfan syndrome 4. Cerebral gigantism (Soto syndrome)
Homocystinuria: •Autosomal recessive •Incidence 1:200,000 •Marfanoid appearance •mental retardation or psychiatric illness Cerebral gigantism (Sotos syndrome) •Large for gestational age, •Mental retardation •Mild hydrocephalus
Growth velocity: Yearly increments of growth; should follow a growth curve Chronologic age (CA): Actual age Bone age (BA): X-ray of left hand and wrist Ideal : CA= BA with normal growth velocity
CA> BA •With normal growth velocity: constitutional delay •With abnormal growth velocity: chronic systemic disease endocrine disorders CA = BA •With normal growth velocity: genetic short stature •With abnormal growth velocity: genetic, chromosomal, syndrome CA< BA •With normal growth velocity: obesity •With abnormal growth velocity: precocious puberty, congenital adrenal hyperplasia (CAH) , hyperthyroidism
Failure to thrive is the failure to gain weight or deceleration of weight growth Risk Factors/ etiology: •Malnutrition (starvation, deprivation, abuse) •Malabsorption (from infection, celiac disease, cystic fibrosis, disaccharidase deficiency, proteinlosing enteropathy) •Allergies •Immune deficiency states •Chronic disease
Presentation: Growth charts •In infants, birth weight is doubled by 4-5 months of age and tripled by 1 year •Patients may show little subcutaneous fat, muscle wasting, rashes , poor tone, weak cry Diagnostic tests: •Hospitalization for documentation of caloric intake and weight gain •CBC, urinalysis, LFT, serum protein •Sweat chloride
•A generalized, excessive over-accumulation of fat •May result from an increase in number or size of adipocytes Risk factors/ etiology: •Parental obesity and family inactivity •Feeding babies as a generic response to any crying •Too much fruit juice in the first year of life •Some syndromes
Presentation: •Tall stature may sometimes be seen •Boys may present with increased adipose tissue in the mammary area •Abdominal striae •A large pubic fat •Puberty may come early •Associated obesity of the proximal extremities common
Diagnostic tests: Body mass index (BMI) > 95% for age/sex or > 30 in adolescents Treatment Exercise and a balanced diet
Complications: •Increased risk for becoming obese adults •Cardiovascular (HTN, increased cholesterol) •Hyperinsulinism •Slipped capital femoral epiphysis •Sleep apnea D/D: •Endocrine causes (Cushing, hypothyroidism, Prader-Willi) •Genetic causes (Turner, Laurence-Moon-Biedl)