The data presented confirm the magnitude of intrauterine growth retardation in developing countries. As summarized in Table 4, we estimate that at least 13.7 million babies in developing countries are already malnourished at birth (IUGR-LBW) every year, representing 11% (ranging from 1.9% to 20.9%) of all newborns in these countries. This rate is considerably higher than that estimated for developed countries, which is approximately 2%. Overall, the incidence of IUGR-LBW is about 6 times higher in developing than in developed countries (Villar et al, 1994).
The estimates for IUGR-LBW should be viewed as a conservative estimation of the magnitude of fetal growth retardation; the actual incidence of IUGR could be considerably higher. For example, if the rate of infants below the 10th percentile of the birth-weight-for-gestational-age reference curve is considered, 23.8%, or approximately 30 million newborns per year, would be affected (Table 4). There are nevertheless some healthy infants with birth weights below the 10th percentile, who represent the lower tail of a fetal growth distribution. However, in most developing countries a large proportion of newborns suffers from some degree of IUGR, as illustrated by the overall downward shift of the birth weight distribution. Unfortunately, a methodology to disentangle these two groups is not available.
The destination employed and the presentation of material on this map do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines represent approximate border lines for which there may not yet be full agreement.
Table 3. Estimated incidence rate of LBW and IUGR-LBW, and expected number of affected newborns in a year
United Nations regions and subregions | Incidence
LBW |
Total
incidence IUGR-LBW |
||
% (< 2500g) |
Total numbers
(thousand) |
% (< 2500g;
³ 37
weeks) |
Total numbers
(thousand) |
|
AFRICA |
NAb |
NAb |
NAb |
NAb |
Eastern Africa |
NAb |
NAb |
NAb |
NAb |
Middle Africa |
21.3 |
792 |
14.9 |
554 |
Northern Africa |
NAb |
NAb |
NAb |
NAb |
Southern Africa |
NAb |
NAb |
NAb |
NAb |
Western Africa |
17.2 |
1628 |
11.4 |
1001 |
ASIA |
18.0d |
14911d |
12.3d |
10147d |
Eastern Asia |
5.8d |
1339d |
1.9d |
463d |
South-central Asia |
28.3 |
11833 |
20.9 |
8739 |
South-eastern Asia |
10.3 |
1308 |
5.6 |
711 |
Western Asia |
8.3 |
431 |
4.5 |
234 |
LATIN AMERICA AND
THE CARIBBEAN |
11.5 |
1370 |
6.5 |
779 |
Caribbean |
11.7 |
84 |
6.7 |
48 |
Central America |
12.3 |
440 |
7.2 |
258 |
South America |
11.1 |
846 |
6.2 |
473 |
OCEANIA |
15.0e |
28.2e |
9.8e |
18.4e |
Melanesia |
15.4 |
28 |
9.9 |
18 |
Micronesia |
NAb |
NAb |
NAb |
NAb |
Polynesia |
4.0 |
0.2 |
0.2 |
0.4 |
DEVELOPING
COUNTRIES |
16.4 |
20423 |
11.0 |
13699 |
DEVELOPED COUNTRIESa |
6.2 |
890 |
NAc |
NAc |
WORLD TOTAL |
15.3 |
21313 |
NAc |
NAc |
a Includes Europe, North America, Australia, New Zealand and Japan.
b Not applicable because coverage of live births < 80%.
c Not applicable because developed status.
d Excludes Japan.
e Excludes Australia and New Zealand.
Table 4. Summary estimates of impaired fetal growth in developing countries
Indicator |
Source |
Rate (%) |
Total
number newborns affected per year¹ |
IUGR-LBW (<
2500g; ³
37 wks gestation) |
Live births
weighted average using LBW rates from WHO data bank (WHO, 1992) and regression model
(Villar et al, 1994) |
11.0 (1.9-20.9)² |
13,699,000 |
LBW (< 2500g;
all gestational ages) |
Live births
weighted average using LBW rates from WHO data bank |
16.4 (5.8-28.3) |
20,423,000 |
IUGR (< 10th
percentile; all gestational ages) |
From WHO
Collaborative Study on Maternal Anthropometry and Pregnancy Outcomes (WHO, 1995b) |
23.8 (9.4-54.2) |
29,639,000 |
¹ Total live births for 1995 are based on the UN World Population Prospects (UN, 1995).
² Range.
The risk of being born IUGR-LBW is highest in Asia (mainly South-central Asia), followed by Africa (Middle and Western Africa), Oceania (Melanesia), and the Latin American region. However, the number of total live births in each geographical region has the effect of making the geographical distribution even more unequal; nearly 75% of all affected newborns are born in Asia - mainly in South-central Asia-20% in Africa, and about 5% in Latin America. The developing countries of Oceania contribute very little to the absolute number of IUGR-LBW because there were only 187,000 live births reported in this region in 1995.
Major constraints to deriving the above estimates included both the qualitative and quantitative limitations of the available data. Moreover, the assessment of the relative contribution of IUGR to total incidence of LBW is conservative given that we used a regression model that underestimates IUGR-LBW by an average of 1.5% (95% CI: - 2.5 to -0.4). These constraints notwithstanding, we nevertheless consider this to be a valid attempt to quantify the magnitude and geographical distribution of IUGR; not only does it provide an incentive for improving data quality, but it is also a suitable means for identifying those countries where population-wide interventions to prevent and control IUGR are urgently required.
In addition to improving the availability and quality of birth weight data, there is a compelling need for feasible measures to assess gestational age or fetal growth. The World Health Organization has recently recommended that countries implement simplified data collection systems for all deliveries and encourage the systematic collection of population-based data on birth-weight-for-gestational-age (WHO, 1995a). Nevertheless, this recommendation is unlikely to be followed by the majority of the developing countries in the near future given the difficulties inherent in obtaining valid assessments of gestational age. Therefore, at the present time, our estimates of IUGR-LBW represent a good public health approximation for descriptive and epidemiological purposes.
A prevalence of IUGR in excess of 20% has been recommended as the cut-off point for triggering public health action. In the absence of information on gestational age, a prevalence of > 15% of LBW may be used as a proxy cut-off (WHO, 1995a). As shown in Table 4, Figure 4 and Appendix I, many developing countries currently exceed these trigger levels for action and, thus, population-wide interventions are urgently needed in these settings. Unfortunately a systematic review of 126 randomized controlled trials (RCT) evaluating 36 interventions to prevent or treat impaired fetal growth has shown that most of them did not show any significant effect on short-term perinatal outcomes (Gülmezoglu et al, 1997). There were, nevertheless, a few interventions that are likely to be beneficial: smoking cessation, balanced protein/energy supplementation and antimalarial chemoprophylaxis in primi-gravidae. Other interventions such as zinc, folate and magnesium supplementation during gestation merit further research. Appropriate combinations of interventions should also be evaluated since it is more likely that a synergistic approach will reduce a multicausal outcome like IUGR.
In summary, the data presented confirm that intrauterine growth retardation is a major public health problem worldwide. Fetuses who suffer from growth retardation have higher perinatal morbidity and mortality (Williams et al, 1982; Balcazar and Haas, 1991; Villar et al, 1990), and are at an increased risk of sudden infant death syndrome (Øyen et al, 1995). During childhood they are more likely to have poor cognitive development (Paz et al, 1995; Low et al, 1992) and neurologic impairment (Parkinson et al, 1981; Taylor and Howie, 1989; Villar et al, 1984); in adulthood they are at increased risk of cardiovascular disease (Osmond et al, 1993), high blood pressure (Williams et al, 1992), obstructive lung disease (Barker, 1991), diabetes (Hales et al, 1991), high cholesterol concentrations (Barker et al, 1993) and renal damage (Hinchliffe et al, 1992). Moreover, IUGR contributes to closing the intergenerational cycle of poverty, disease and malnutrition. The implications of this vicious cycle are enormous both in terms of human and socioeconomic development of the affected populations. Country-wide interventions aimed at preventing fetal growth retardation are urgently needed. A good start in life will pay off, both in terms of human capital and economic development.
Acknowledgements - We are
grateful to Mrs Elisabeth Åhman from the WHO Maternal Health and Safe Motherhood
Programme for kindly providing us with the latest version of the WHO Database on Low Birth
Weight.
Altman DG & Hytten FE(1989): Intrauterine growth retardation: lets be clear about it. Br J. Obstet. Gynaecol 96, 1127 - 1132.
Balcazar H & Haas ID (1991): Retarded fetal growth patterns and early neonatal mortality in a Mexico city population. Bull Pan. Am. Health Organ. 25, 55-63.
Barker DJ, Martyn CN, Osmond C, Hales CN & Fall CH (1993): Growth in utero and serum cholesterol concentrations in adult life. BMJ 307, 1524-1527.
Barker DJP (1991): The intrauterine origins of cardiovascular and obstructive lung disease in adult life: The Mark Daniels lecture 1990. J. Royal Coll Phys. London 25, 129-133.
de Onis M & Habicht JP (1996): Anthropometric reference data for international use: recommendations from a World Health Organization Expert Committee. Am. J. Clin. Nutr. 64, 650-658.
Gülmezoglu M, de Onis M & Villar J (1997): Effectiveness of interventions to prevent or treat impaired fetal growth. Obstet. Gynecol Surv. 52, 139-149.
Hales CN, Barker DJ, Clark PM et al (1991): Fetal and infant growth and impaired glucose tolerance at age 64. BMJ 303, 1019-1022.
Hinchliffe SA, Lynch MR, Sargent PH, Howard CV & Van Velzen D (1992): The effect of intrauterine growth retardation on the development of renal nephrons. Br. J. Obstet Gynaecol 99, 296-301.
Kleinbaum DG, Kupper LL & Muller KE (1988): Applied regression analysis and other multivariable methods. PWS-KENT Publishing Company: Boston. Pp 41-79.
Low J. Handley-Derry M, Burke S et al (1992): Association of intrauterine fetal growth retardation and learning deficits at age 9 to 11 years. Am. J. Obstet Gynecol 167, 1499-1505.
Martin Bland JM & Altman DG (1986): Statistical methods for assessing agreement between two methods of clinical measurement. Lancet i, 307-310.
Osmond C, Barker DJ, Winter PD, Fall CH & Simmonds SJ (1993): Early growth and death from cardiovascular disease in women. BMJ 307, 1519-1524.
Øyen N. (Skjærven R. Little R & Wilcot A (1995): Fetal growth retardation in Sudden Infant Death Syndrome (SIDS) babies and their siblings. Am. J. Epidemiol. 142, 84-90.
Parkinson CE, Wallis S & Harvey DR (1981): School achievement and behaviour of children who are small-for-dates at birth. Dev. Med. Child. Neurol. 23, 41-50.
Paz I, Gale R. Laor A, Danon YL, Stevenson DK & Seidman DS (1995): The cognitive outcome of full term small for gestational age infants at late adolescence. Obstet. Gynecol 85, 452-456.
Puffer R & Serrano C (1987): Patterns of birthweight. PAHO Scientific Publication No. 504. Pan American Health Organization: Washington. Pp 50-65.
Taylor DJ & Howie PW (1989): Fetal growth achievement and neurodevelopmental disability. Br J. Obstet Gynaecol 96, 789-794.
UN (1995): UN world population prospects - the 1994 revision. United Nations: New York.
Villar J & Belizán JM (1982): The relative contribution of prematurity end fetal growth retardation to low birth weight in developing and developed societies. Am. J. Obstet. Gynecol. 143, 793-798.
Villar J, Smeriglio V, Martorell R. Brown CH & Klein RE (1984): Heterogenous growth and mental development of intrauterine growth-retarded infants during the first three years of life. Pediatrics 74, 783-791.
Villar J, de Onis M, Kestler E, Bolanos F. Cerezo R. Berendes H (1990): The differential morbidity of the intrauterine growth retardation syndrome. Am. J. Obstet. Gynecol. 163, 151-157.
Villar J. Ezcurra EJ, Gurtner de la Fuente V & Campodonico L (1994): Pre-term delivery syndrome: the unmet need In New Perspectives for the effective treatment of pre-term labor: an international consensus. Research and Clinical Forums; 16, pp 9-38.
WHO (1992): Low birth weight - a tabulation of available information. Maternal Health and Safe Motherhood Programme, Geneva, WHO/MCH/92.2. Updated version of September 1996. World Health Organization: Geneva.
WHO (1995a): Physical status: the use and interpretation of anthropometry. Report of a WHO Expert Committee, pp. 121-160. Technical Report Series No. 854. World Health Organization: Geneva.
WHO (1995b): Maternal anthropometry and pregnancy outcomes - A WHO collaborative study. Bull WHO 73 (Suppl.), 1-98.
Williams RL, Creasy RK, Cunningham GC, Hawes WE, Norris FD & Tashiro M (1982): Fetal growth and perinatal viability in California. Obstet. Gynecol 59, 624-632.
Williams S. George I, Silva P
(1992): Intrauterine growth retardation and blood pressure at age seven and eighteen. J.
Clin. Epidemiol 45, 1257-1263.