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close this bookCauses and Consequences of Intrauterine Growth Retardation, Proceedings of an IDECG workshop, November 1996, Baton Rouge, USA, Supplement of the European Journal of Clinical Nutrition (International Dietary Energy Consultative Group - IDECG, 1996, 100 pages)
close this folderSocioeconomic determinants of intrauterine growth retardation
View the document(introductory text...)
View the documentIntroduction
View the documentSocioeconomic disparities in IUGR: Mediating factors
View the documentSecular trends in IUGR and its determinants
View the documentAre there residual socioeconomic disparities in IUGR?
View the documentReferences
View the documentDiscussion

(introductory text...)

MS Kramer

Correspondence: Dr MS Kramer

Departments of Pediatrics and of Epidemiology and Biostatistics, McGill University, Faculty of Medicine, 1020 Pine Avenue West, Montreal, Quebec H3A 1A2, Canada

This paper reviews the evidence bearing on socioeconomic determinants of intrauterine growth retardation (IUGR). The primary focus is on those factors with a quantitatively important impact from a public health perspective, as indicated by their large etiologic fraction (population attributable risk). In developed countries in which a sizeable proportion of women smoke during pregnancy, cigarette smoking is associated with the largest etiologic fraction (by far), followed by low gestational weight gain (primarily due to low energy intake) and low pre-pregnancy body mass index (BMI). In developing countries where undernutrition is prevalent and pregnant women do not smoke, low maternal weight gain and BMI assume even greater importance, as does short maternal stature.

A major section of the paper concerns the large within-country socioeconomic disparities in IUGR and the possible mechanisms underlying these disparities. In developed countries, differences in cigarette smoking explain a large part of the disparity; low weight gain and short stature may also be important mediators in some settings. Future etiologic studies should assess a wide scope of potential determinants and will require large sample sizes to control for their mutually confounding effects.

Introduction

One of the most robust findings in epidemiologic research on the etiology of low birth weight (LBW) has been the large socioeconomic disparities in both intrauterine growth retardation (IUGR) and preterm birth (Kramer, 1987; Parker et al, 1994; Wilcox MA et al, 1995; Kogan, 1995). In a now classic paper, Villar and Belizan reported data from 11 different regions in developed countries and 25 in developing countries (Villar and Belizan, 1982). Their analysis indicated that in developing countries, most low birth weight is due to IUGR, whereas in developed countries (especially those with the lowest LBW rates), most is due to preterm birth (Villar and Belizan, 1982). Most of the differences in LBW rates between developed and developing countries appear attributable to an increased prevalence of IUGR, rather than preterm birth, with relative risks of 6.6 and 2.0, respectively (Villar and Belizan, 1982).

Even within developed countries, however, socioeconomic disparities in birth weight have been consistently reported. These disparities occur not only in countries like the United States (Parker et al, 1994), with vast differences between the rich and the poor, but even in more 'socialistic' countries like Canada (Wilkins et al, 1991), Sweden (Ericson et al, 1993), and Denmark (Olsen and Frische, 1993) with less extreme contrasts of wealth and poverty and with universal access to high-quality prenatal and other medical care. In multiracial countries, IUGR rates have been shown to differ considerably by race, with increased IUGR rates among blacks in the U.S. (Horon et al, 1983; Showstack et al, 1984; Linn et al, 1983), aboriginals in Australia (Seward and Stanley, 1981; Sayers and Powers, 1993), and Asians in the U.K. (Dawson and Golder, 1982; Moore et al, 1995). Although a small portion of the difference may be due to true biological differences between the racial groups (Wen et al, 1995), much of it is probably linked to socioeconomic disadvantage among these racial groups. Interestingly, some other minority groups do not have the same apparent problem with IUGR. These include American Indian groups in Canada (Munroe et al, 1984; Thomson, 1990), North African immigrants in Israel (Yudkin et al, 1983), and Mexican immigrants in the U.S. (Guendelman and English, 1995); despite their socioeconomic disadvantage relative to the predominant racial/ethnic groups, these groups show birth weight distributions shifted somewhat to the right relative to the distributions dominant in their respective countries, with correspondingly low rates of IUGR.

Socioeconomic disparities in IUGR: Mediating factors

Having more money or education probably has no direct effect on how fast a fetus grows in utero. In other words, socioeconomic disadvantage is probably not a direct, independent determinant of fetal growth. Rather, socioeconomic disadvantage may lead to adverse psychological, behavioral, or other environmental exposures that restrict fetal growth. It is important to understand these direct-acting etiologic determinants, both in terms of their relative risks and their etiologic fractions. The relative risk (RR) indicates how much more likely the adverse outcome (IUGR in this case) occurs in women with vs those without a given risk factor; the RR is a measure of the strength of association between the risk factor and IUGR. The etiologic fraction (also know as the population attributable risk or attributable fraction) reflects both the relative risk of a given risk factor and its prevalence in the population of interest. It is defined as the proportion of IUGR occurring in a population that can be attributed to the risk factor or, equivalently, the proportion of IUGR in the population that would theoretically disappear if exposure to the risk factor were eliminated. The etiologic fraction (EF) can be estimated as follows:


where P is the prevalence of the risk factor and RR its corresponding relative risk for IUGR (Levin, 1953). Thus the relative risk compares the risk in individual women with and without the risk factor, while the etiologic fraction reflects the population burden of IUGR due to the risk factor.

Much is known about the attributable causes of IUGR, which are depicted schematically in the Figure. In this pie diagram, the size of the pie slice corresponding to each determinant is a rough indication of its importance (in terms of etiologic fraction) relative to the other determinants shown in the pie. It is an updated version originally based on a meta-analysis of the English- and French-language literature published between 1970 and 1984 (Kramer, 1987). The diagram should be interpreted in relative terms only; because the determinants shown are not mutually exclusive, any given woman may have more than one of them. Thus, the total etiologic fraction of all the determinants of IUGR is less than the 100% suggested by the diagram (Bruzzi et al, 1985).

The Figure represents a developed country setting in which approximately 30% of the women smoke cigarettes during pregnancy. In this type of setting, the risk factors with the highest relative risks are pre-eclampsia and cigarette smoking. Because cigarette smoking is so much more prevalent than pre-eclampsia, however, cigarette smoking is associated with a far higher etiologic fraction, i.e., its corresponding pie slice is much larger. Other factors with high etiologic fractions (representing somewhat lower relative risks but high prevalences) include low gestational weight gain (partially, but not exclusively, reflecting low energy intake), low prepregnancy body mass index (BMI), primiparity, short maternal stature, and nonwhite racial/ethnic origin. High levels of alcohol consumption (two or more drinks per day) (Zuckerman and Hingson, 1986; Walpole et al, 1990) and the use of marijuana or cocaine (Hatch and Bracken, 1986; Zuckerman et al, 1989; Shiono et al, 1995) may also restrict fetal growth, but their etiologic fractions are quite low, owing to low prevalences of exposure. The effect of high caffeine consumption (> 300 mg/day) is more controversial; although such consumption is highly prevalent, its corresponding relative risk is only modestly (if at all) elevated (Martin and Bracken, 1987; Dlugosz and Bracken, 1992; Fortier et al, 1993).


Figure. Attributable causes of intrauterine growth retardation (developed country).

In a developing country setting in which pregnant women do not smoke cigarettes, the pie diagram would look quite different. The 'slice' corresponding to cigarette smoking would disappear, while the slices corresponding to low weight gain, low prepregnancy BMI, and short stature would increase in size considerably. In addition, malaria would occupy a substantial slice in those settings where the disease is endemic.

For a risk factor to be an important mediating variable between socioeconomic disadvantage and IUGR, it must satisfy two criteria. First, it must have a high etiologic fraction for IUGR. Second, it must be strongly associated with socioeconomic status, i.e., it should be far more prevalent in low-SES population groups. The main candidates for such mediating variables of IUGR include maternal nutritional factors (maternal stature, prepregnancy body mass index, and energy balance, i.e., gestational weight gain); cigarette smoking; alcohol consumption; narcotic, cocaine, marijuana, and other drug exposure; maternal work during pregnancy; and stress, anxiety, and other psychological factors. A review of the literature of the evidence concerning maternal nutritional determinants of IUGR is the subject of another paper in this supplement. My mandate is to focus on the evidence concerning the non-nutritional factors. Nonetheless, I will begin by briefly reviewing the evidence concerning the relationship between maternal nutrition and socioeconomic disparities in IUGR.

Low prepregnancy BMI is certainly not an explanation for socioeconomic disparities in IUGR in developed country settings, since BMI is inversely associated with socioeconomic status (in other words, BMIs are higher in women of low socioeconomic status) (Flegal et al, 1988). Low BMI may be an important factor in developing countries, however, at least in those developing countries where maternal obesity is less of a problem than it is in most industrialized countries. In countries with high prevalences of maternal undernutrition, it is reasonable to presume that undernutrition is more prevalent among those from unfavorable socioeconomic backgrounds, and thus low prepregnancy BMI could be partly responsible for high IUGR rates seen among the poor in many developing countries. Maternal stature is known to be associated with socioeconomic status, although the direction of cause-and-effect is far from certain (Thomson and Billewicz, 1963). Nonetheless, in developed country settings, differences in stature according to socioeconomic status are small and, given the modest etiologic fraction for maternal stature, unlikely to explain a sizeable portion of socioeconomic disparities in IUGR. Gestational weight gain has also been reported to vary by SES (Taffel, 1986). Low weight gains appear to be more common in women with low educational attainment, while high weight gains are more prevalent among the highly educated (Taffel, 1986). Given the large etiologic fraction associated with low gestational weight gain, this may well represent an important mechanism for the high rate of IUGR among the socioeconomically disadvantaged.

Smoking is probably the most important variable mediating socioeconomic disparities in IUGR in developed country settings. In most such settings, cigarette smoking is both far more common and heavier (i.e., larger number of cigarettes smoked per day) in women from lower socioeconomic backgrounds (Subcommittee on Nutritional Status and Weight Gain During Pregnancy et al, 1990; Hagland et al, 1993). Moreover, as the adverse effects of smoking in pregnancy have become widely recognized by physicians and the general public, the socioeconomic gradient in cigarette smoking has widened (Subcommittee on Nutritional Status and Weight Gain During Pregnancy et al, 1990).

Studies of strenuous work and physical activity during pregnancy have focused on preterm birth (Mamelle et al, 1984; Saurel-Cubizolles and Kaminski, 1987; Homer et al, 1990; Henriksen et al, 1995). Although most epidemiologic studies have not found that prolonged standing or strenuous activity at work is associated with IUGR, there are a few exceptions (Launer et al, 1990; Henriksen et al, 1995). Because a very small fraction of women are exposed to prolonged standing or walking at work, however, its etiologic fraction is likely to be extremely low, i.e., it is not an important mediating variable for socioeconomic disparities in IUGR. Vigorous aerobic exercise that continues into the third trimester may be associated with a slight increase in IUGR (Clapp and Dickstein, 1984), although here too, the small number of women engaging in vigorous exercise during this critical period of fetal growth strongly suggests that it is not an important mediating variable from a population perspective.

Finally, epidemiologists have become increasingly interested in stress, anxiety, and other psychological factors as risk factors for adverse pregnancy outcomes. Although most of the evidence for the adverse effects of these psychological factors bears on preterm birth (Nuckolls et al, 1972; Newton and Hunt, 1984; Lou et al, 1992; Lobel et al, 1992; Nordentoft et al, 1996) and suggests no effect on fetal growth (Nordentoft et al, 1996; Aarts and Vingerhoets, 1993; Hedegaard et al, 1996), one study suggests a possible association with IUGR in thin women (Cliver et al, 1992). An overview (meta-analysis) of clinical controlled trials shows little if any benefit of social support on IUGR, with a pooled odds ratio of 1.06 and a 95% confidence interval of 0.86-1.30 (Hodnett, 1994). None of these trials, however, has demonstrated the effectiveness of the social support in correcting or reducing the stress, anxiety, or depression of the women who are offered the intervention.

Secular trends in IUGR and its determinants

Both Canada and the United States have witnessed a modest decline in the incidence of low birth weight over the last two decades. Most or all of this decline is due to a lower incidence of IUGR, rather than of preterm birth (Ng and Wilkins, 1994; Kessel et al, 1984; Division of Nutrition, National Center for Chronic Disease Prevention and Health Promotion, 1994). In Canada, the birth weight of term infants increased approximately 130-140 grams between 1972 and 1986, with no apparent change in the gestational age distribution or in the growth in infants delivered preterm (Arbuckle and Sherman, 1989). Thus in both the United States and Canada, the only important change in fetal growth over the last several decades has been an increase in the size of term infants.

Based on simultaneous trends in etiologic determinants, this increase in the size of term births appears to reflect three primary factors: (1) a secular trend toward increasing prepregnancy body mass index (Flegal et al, 1988), reflecting a general trend toward increasing adiposity (which has been particularly evident in North America, but observed in most western countries); (2) a marked secular trend toward higher gestational weight gains, which have increased from 9 or 10 kilograms in the 1950's and 60's to 15 kilograms, on average, in recent years (Taffel; Eastman and Jackson, 1968; Niswander and Jackson, 1974; Keppel and Taffel, 1993); and (3) substantial decreases in cigarette smoking among pregnant women (Kleinman and Kopstein, 1987), presumably in response to increasing knowledge and publicity about the adverse effects of smoking on health, in general, and on pregnancy outcome, in particular.

Are there residual socioeconomic disparities in IUGR?

In an earlier section, I reviewed the evidence concerning factors that may mediate the socioeconomic disparities in IUGR incidence. Leading candidates for quantitatively important (from a population perspective) factors include cigarette smoking (both frequency and severity), low gestational weight gain (presumably due to low energy intake), and short stature. Alcohol, drugs of abuse, and maternal work and physical activity may explain a small, additional portion of the disparity. But can the entire socioeconomic gradient in IUGR be explained by the above-mentioned risk factors? This is an important question for both perinatal epidemiologists and public health policy makers. Unfortunately, the answer is unknown. Most research in this area has tended to focus on one or two factors at a time. Few have adequately measured all of these potentially mediating variables, and most have had insufficient sample sizes to do so. Thus it is unknown whether any residual socioeconomic disparities remain after accounting (controlling) for known, or strongly suspected, mediating variables. This is a promising area for future research that may not only uncover new etiologic determinants of IUGR, but also help reduce its high incidence among the socially disadvantaged.

References

Aarts MCG & Vingerhoets AJJM (1993): Psychosocial factors and intrauterine fetal growth: a prospective study. J. Psychosom. Obstet. Gynaecol. 14, 249-258.

Arbuckle TE & Sherman GJ (1989): An analysis of birth weight by gestational age in Canada. Can. Med. Assoc. J. 140, 157-165.

Bruzzi P, Green SB, Byar DP, Brinton LA & Schairer C (1985): Estimating the population attributable risk for multiple risk factors using case-control data. Am. J. Epidemiol. 122, 904-914.

Clapp JF & Dickstein S (1984): Endurance exercise and pregnancy outcome. Med. Sci. Sport 16, 556-562.

Cliver SP, Goldenberg RL, Cutter GR, Hoffman HJ, Copper RL, Gotlieb SJ & Davis RO (1992): The relationship among psychosocial profile, maternal size, and smoking in predicting fetal growth retardation. Obstet. Gynecol. 80, 262-267.

Dawson I & Golder RY (1982): Birthweight by gestational age and its effect on perinatal mortality in white and in Punjabi births: experience at a district general hospital in West London 1967-1975. Br. J. Obstet. Gynaecol. 89, 896-899.

Division of Nutrition, National Center for Chronic Disease Prevention and Health Promotion (1994): Increasing incidence of low birth weight - United States, 1981-1991. 43, 335-339.

Dlugosz L & Bracken MB (1992): Reproductive effects of caffeine: a review and theoretical analysis. Epidemiol. Rev. 14, 83-100.

Eastman NJ & Jackson E (1968): Weight relationships in pregnancy: I. The bearing of maternal weight gain and pre-pregnancy weight on birth weight in full term pregnancies. Obstet. Gynecol. Surv. 23, 1003-1025.

Ericson A, Eriksson M, Källén B & Zetterström R (1993): Methods for the evaluation of social effects on birth weight-experiences with Swedish population registries. Scand. J. Soc. Med. 2, 69-76.

Flegal KM, Harlan WR & Landis JR (1988): Secular trends in body mass index and skinfold thickness with socioeconomic factors in young adult women. Am. J. Clin. Nutr. 48, 535-543.

Fortier I, Marcoux S & Beaulac-Baillargeon L (1993): Relation of caffeine intake during pregnancy to intrauterine growth retardation and preterm birth. Am. J. Epidemiol. 137, 931-940.

Guendelman S & English PB (1995): Effect of United States residence on birth outcomes among Mexican immigrants: an exploratory study. Am. J. Epidemiol. 142, S30-S38.

Hagland B, Cnattingius S & Nordström M-L (1993): Social differences in late fetal death and infant mortality in Sweden 1985-86. Paediatr. Perinat. Epidemiol. 7, 33-44.

Hatch EE & Bracken MB (1986): Effect of marijuana use in pregnancy on fetal growth. Am. J. Epidemiol 124, 986-993.

Hedegaard M, Henriksen TB, Sabroe S & Secher NJ (1996): The relationship between psychological distress during pregnancy and birth weight for gestational age. Acta Obstet. Gynecol. Scand. 75, 32-39.

Henriksen TB, Hedegaard M & Secher NJ (1995): Standing and walking at work and birthweight. Acta Obstet. Gynecol Scand 74, 509-516.

Henriksen TB, Hedegaard M, Secher NJ & Wilcox AJ (1995): Standing at work and preterm delivery. Br. J. Obstet. Gynaecol. 102, 198-206.

Hodnett ED (1994): Support from caregivers during at-risk pregnancy. In: Enkin MW, Keirse MJNC, Renfrew MJ, Meilson JP (eds). Pregnancy and Childbirth Module. 'Cochrane Database of Systematic Reviews': Review No. 04169, 27 April 1994. Published through 'Cochrane Updates on Disk.' Oxford: Update Software, Disk Issue I.

Homer CJ, Beresford SAA, James SA, Siegel E & Wilcox S (1990): Work related physical exertion and risk of preterm, low birthweight delivery. Paediatr. Perinat. Epidemiol. 4, 161-174.

Horon IL, Strobino DM & MacDonald HM (1983): Birth weights among infants born to adolescent and young adult women. Am. J. Obstet. Gynecol 146, 444-449.

Keppel KG & Taffel SM (1993): Pregnancy-related weight gain and retention: implications of the 1990 Institute of Medicine guidelines. Am. J. Public Health 83, 1100-1103.

Kessel SS, Villar J. Berendes HW & Nugent RP (1984): The changing pattern of low birth weight in the United States, 1970 to 1980. JAMA 251, 1978-1982.

Kleinman JC & Kopstein A (1987): Smoking during pregnancy, 1967-80. Am J. Public Health 77, 823-825.

Kogan MD (1995): Social causes of low birth weight. J. R. Soc. Med. 88, 611-615.

Kramer MS (1987): Determinants of low birth weight: methodological assessment and meta-analysis. Bull. WHO 65, 663-737.

Launer LJ, Villar J. Kestler E & De Onis M (1990): The effect of maternal work on fetal growth and duration of pregnancy: a prospective study. Br. J. Obstet. Gynaecol 97, 62-70.

Levin ML (1953): The occurrence of lung cancer in man. Acta Unio Internationalis Contra Cancrum 19, 531-541.

Linn S. Schoenbaum SC, Monson RR, Rosner R. Stubblefield PC & Ryan KJ (1983): The association of marijuana use with outcome of pregnancy. Am. J. Public Health 73, 1161-1164.

Lobel M, Dunkel-Schetter C & Scrimshaw SCM (1992): Prenatal maternal stress and prematurity: a prospective study of socioeconomically disadvantaged women. Health Psychol. 11, 32-40.

Lou HC, Nordentoft M, Jensen F, Pryds O, Nim J & Hemmingsen R (1992): Psychosocial stress and severe prematurity. Lancet 340, 54.

Mamelle N, Laumon B & Lazar P (1984): Prematurity and occupational activity during pregnancy. Am. J. Epidemiol. 119, 309-322.

Martin TR & Bracken MB (1987): The association between low birth weight and caffeine consumption during pregnancy. Am. J. Epidemiol. 126, 813-821.

Moore WMO, Bannister RP, Ward BS, Hillier VF & Bamford FN (1995): Fetal and postnatal growth to age 2 years by mother's country of birth. Early Hum. Dev. 42, 111-121.

Munroe M, Shah CP, Badgley R & Bain HW (1984): Birth weight, length, head circumference and bilirubin level in Indian newborns in the Sioux Lookout Zone, Northwestern Ontario. Can. Med. Assoc. J. 131, 453-456.

Newton RW & Hunt LP (1984): Psychosocial stress in pregnancy and its relation to low birth weight. Br. Med. J. 288, 1191-1194.

Ng E & Wilkins R (1994): Maternal demographic characteristics and rates of low birth weight in Canada, 1961 to 1990. Health Rep. 6, 241-252.

Niswander K & Jackson EC (1974): Physical characteristics of the gravida and their association with birth weight and perinatal death. Am. J. Obstet. Gynecol. 119, 306-313.

Nordentoft M, Lou HC, Hansen D, Nim J, Pryds O, Rubin P & Hemmingsen R (1996): Intrauterine growth retardation and premature delivery: the influence of maternal smoking and psychosocial factors. Am. J. Public Health 86, 347-354.

Nuckolls KB, Cassel J & Kaplan BH (1972): Psychosocial assets, life crisis, and the prognosis of pregnancy. Am. J. Epidemiol, 95, 431-441.

Olsen J & Frische G (1993): Social differences in reproductive health. Scand. J. Soc. Med. 2, 90- 97.

Parker JD, Schoendorf KC & Kiely JL (1994): Associations between measures of socioeconomic status and low birth weight, small for gestational age, and premature delivery in the United States. Ann. Epidemiol. 44, 271-278.

Saurel-Cubizolles MJ & Kaminski M (1987): Pregnant women's working conditions and their changes during pregnancy: a national study in France. Br. J. Ind. Med. 44, 236-243.

Sayers SM & Powers JR (1993): Birth size of Australian Aboriginal babies. Med. J. Aust. 159, 586-591.

Seward JF & Stanley FJ (1981): Comparison of births to Aboriginal and Caucasian mothers in Western Australia. Med. J. Aust. 2, 80-84.

Shiono PH, Klebanoff MA, Nugent RP, Cotch MF, Wilkins DG, Rollins DG, Carey JC & Behrman RE (1995): The impact of cocaine and marijuana use on low birth weight and preterm birth: a multicenter study. Am. J. Obstet. Gynecol. 172, 19-27.

Showstack J, Budetti PP & Minkler D (1984): Factors associated with birthweight: an exploration of the role of prenatal care and length of gestation. Am. J. Public Health 74, 1003-1008.

Subcommittee on Nutritional Status and Weight Gain During Pregnancy, Food and Nutrition Board, U.S. Institute of Medicine/National Academy of Sciences (1990): Nutrition During Pregnancy. National Academy Press: Washington, D.C.

Taffel SM (1986): Maternal weighs gain and the outcome of pregnancy: United States, 1980. Vital Health Statistics, Series 21, No. 44. DHHS Pub. No. (PHS) 86-1922.

Thomson AM & Billewicz WZ (1963): Nutritional status, maternal physique and reproductive efficiency. Proc. Nutr. Soc. 22, 55-60.

Thomson M (1990): Heavy birthweight in Native Indians of British Columbia. Can. J. Pub. Health 81, 443-446.

Villar J & Belizan, JM (1982): The timing factor in the pathophysiology of the intrauterine growth retardation syndrome. Obstet. Gynecol. Surv. 37, 499-506.

Walpole I, Zubrick S & Pontré J (1990): Is there a fetal effect with low to moderate alcohol use before or during pregnancy? J. Epidemiol. Comm. Health 44, 297-301.

Wen SW, Kramer MS & Usher RH (1995): Comparison of birth weight distributions between Chinese and Caucasian infants. Am. J. Epidemiol. 141, 1177-1187.

Wilcox MA, Smith SJ, Johnson IR, Maynard PV & Chilvers CE (1995): The effect of social deprivation on birthweight, excluding physiological and pathological effects. Br. J. Obstet. Gynaecol. 102, 918-924.

Wilkins R, Sherman G & Best PAF (1991): Birth outcomes and infant mortality by income in urban Canada, 1986. Health Rep 3, 7-31.

Yudkin PL, Harlap S & Baras M (1983): High birthweight in an ethnic group of low socioeconomic status. Br. J. Obstet. Gynaecol. 90, 291-296.

Zuckerman B, Frank DA, Hingson R, Amaro H, Levenson SM, Kayne H, Parker S, Vinci R, Aboagye K, Fried LE, Cabral H, Timperi R & Bauchner H (1989): Effects of maternal marijuana and cocaine use on fetal growth. N. Engl. J. Med. 320, 762-768.

Zuckerman BS & Hingson R (1986): Alcohol consumption during pregnancy: a critical review. Dev. Med. Child Neurol. 28, 649-661.

Discussion

The mother's nutritional status before conception (reflected by maternal BMI) and her weight gain during pregnancy are important determinants of fetal growth in developing countries and, to a somewhat lesser extent, in developed countries. In initially thinner women, the effect of weight gain on fetal growth is greater than in fatter ones. In very thin women, even a high weight gain during pregnancy may not be able to fully compensate (even with the interaction effect) the higher risk of having an IUGR baby. Being well-nourished before conception has a buffering effect and, in women with a prepregnancy BMI > 27, weight gain during pregnancy will no longer have much of an effect on fetal growth.

The Subcommittee on Nutritional Status and Weight Gain During Pregnancy of the US Institute of Medicine made recommendations in 1990, recognizing the relationship between prepregnancy BMI and desirable weight gain, but looking at outcomes in babies, not mothers. It recommended weight gains that, throughout the range of prepregnancy BMIs, were considerably higher than recommendations in other countries, including Europe. Several authors have drawn attention to the fact that the residual weight the mother retains after giving birth is dependent on the weight she gained during pregnancy. If recommended weight gains during pregnancy are relatively high, this results in a tendency to increasing BMIs after each pregnancy and can become a public health concern. The effects of recommending high weight gains during pregnancy on the birthweight distribution is less clear; a shift to the right would mean fewer IUGR babies and that would be an advantage; but it would also mean more macrosomic babies and possibly more complications at birth and a greater percentage of mothers needing Cesarean sections, which would be a disadvantage. An intriguing observation is that black women in the US tend to have babies with a lower mean birth weight, even though their body weight tends to be higher than that of white women. Making recommendations on weight gains during pregnancy is not an aim of this workshop, but several discussants are of the opinion that the next committee that will be charged with making such recommendations in the US may have to correct current estimates downwards.

A more general question is whether making recommendations has any effect on observed weight gains. What little literature exists on this subject suggests that recommendations given by health providers to pregnant women can and often do result in a change in knowledge but rarely produce changes in behavior and practice. Three randomized trials on the effect of nutritional advice given to pregnant women are not very strong methodologically. They show only a very modest effect on maternal weight gain and practically no effect on birthweight. On the other hand, it looks as if a more relaxed, less restrictive general attitude towards weight gain has led to a secular increase in birthweight, primarily among term infants. Unfortunately, this would also affect women with a high prepregnancy BMI.

A widely held belief is that since fetal growth is greatest in the third trimester, interventions are also likely to have their greatest effect during the third trimester. The Dutch women whose third trimester of pregnancy coincided with the famine towards the end of WW2 were the ones who gave birth to the lightest babies, and in The Gambia the prevalence of LBW babies is highest in women whose third trimester of pregnancy coincides with the hungry season in summer. Dietary supplementation of Taiwanese women before and during the whole pregnancy did not have more of an effect on birthweight than did similar supplementation trials during the last trimester only. However, the evidence bearing on earlier nutritional effects is not completely uniform. A study among adolescents showed that greater weight gain early in pregnancy had more of an effect than larger weight gains later. A study of rural Guatemalan women showed an interaction between gastrointestinal parasitosis and maternal height. In women of average height and weight, mebendazol therapy had little effect on birthweight, but in short women it did. In this study too, therapy had a greater effect during the first half of pregnancy than during the second half.

The assumption is frequently made that early growth restriction will result in small but proportionate babies, whereas growth restriction during the latter part of pregnancy will result in wasted babies of approximately normal length. Kramer argued that this generalization had its limits because of a strong association between wasting and severity of growth restriction. The theory explaining the high rate of growth-retarded babies born to teenagers by a competition for nutrients received support from a recent study in which knee height (as an indicator of bone growth) was monitored in pregnant teenage mothers. The birthweights of the babies were inversely related to maternal bone growth.

Genital and urinary tract infections seem to result more in preterm births than in IUGR.