![]() |
|
|
March of Dimes Birth Defects Foundation, California Birth Defects Monitoring Program, Oakland, CA 94606
3 To whom correspondence should be addressed. E-mail: gsh{at}cbdmp.org.
| ABSTRACT |
|---|
|
|
|---|
KEY WORDS: pregnancy developing countries micronutrients epidemiology strenuous work
Does strenuous work by women during pregnancy in developing countries influence micronutrient status and thereby increase risks of adverse pregnancy outcomes? Furthermore, does strenuous physical activity in the workplace lead to micronutrient compromise that leads to adverse pregnancy outcomes?
Some data exist about the potential relationship between strenuous work or physical activity and nutrient compromise, strenuous work or physical activity and adverse reproductive outcomes and micronutrient intakes or status and adverse reproductive outcomes. However, no substantial body of data exists that has directly investigated the entire potential causal cascade posed by the above questions.
A search of the literature identified only a few papers from developing countries that provided even remotely related data on the topic. Prentice et al. (1, 2) and Ceesay et al. (3) observed that among Gambian women who were supplemented, an effect of supplementation could be observed on birth weight. The effect appeared to be seasonal and to be among women who performed greater field work activities and who had lower food supplies. The supplement in the Prentice et al. studies consisted of a net energy increase of approximately 431 kcal/d, protein, calcium, riboflavin and vitamins A and C. In the season of greatest food shortage and highest workload, women who were supplemented had a reduction from 28% to 5% in the prevalence of low-birth-weight babies.
Another pertinent example is an investigation of a population in Pune, India (4). Increased physical activity, as measured by work in farming or gathering water, was associated with infants of low birth weight, smaller head circumference, smaller mid-arm circumference and lower placental weight. These associations were observed after maternal energy and protein intake were controlled for. Information about effects that micronutrient intakes may have had on the observed association were not given.
Because of the lack of empirical data, this brief review will piece together some of the available epidemiologic evidence, primarily from studies conducted in developed countries, that may facilitate inferences. The three areas for which some epidemiologic data are available are strenuous work or physical activity and nutrient compromise, strenuous work or physical activity and adverse reproductive outcomes, and micronutrient status and adverse reproductive outcomes.
Strenuous work and nutritional compromise: epidemiologic evidence
A few dietary energy studies were conducted in women from less developed countries (5 9). A study in Guatemala (5) estimated the energy costs associated with 32 household and agricultural activities performed by peasant women. A study of Gambian women observed that most tasks performed by these women were deemed light or moderate from the perspective of energy expenditures and did not appear to vary based on stage of pregnancy (8). These studies tend to include relatively small numbers of subjects, only a small proportion of whom are pregnant, and do not provide information on the influence of such activities on micronutrient status.
Bendich (10) suggested an indirect effect, although not a biological mechanism, that employment can have on the nutritional status of pregnant women. That is, women who are employed may be at risk of compromised diets because of reduced time for shopping and cooking. Associated with this speculation is the finding that working women who worked standing were less likely to eat three meals per day than were women who worked in occupations that did not require prolonged standing (11).
The implication of physical strain or activity in the workplace on nutritional status of the pregnant woman is subject to a number of considerations. Foremost is what is being measured. For example, energy expenditure averaged over tasks may not be the relevant measure. Peak energy expenditures such as lifting may be more important than averaged expenditures over longer time periods. Measurement of an activity such as lifting and correlation with energy expenditure is a good example of the measurement complexities: lifting may result in a greater intraabdominal pressure, which could be the potential mechanism for the adverse reproductive outcome rather than increased energy or nutrient expenditure. As noted by Eskenazi et al. (12), type of physical exertion, amount of exertion and the context of the exertion are likely to be relevant to this body of literature. Furthermore, not all physical strain is equal. For example, comparing recreational physical exercise versus workplace physical strain (e.g., long work hours) reflects the difference in the degree of voluntarism between recreational and leisure time activity and physical activity at work (13, 14).
The relationships between physical activity, namely exercise, and nutritional effects on pregnant women are complex. For example, a recent study showed that moderate-intensity exercise (weight bearing) reduces fetoplacental growth and size at birth (15).
Strenuous work and reproductive outcomes: epidemiologic evidence
A number of mechanisms have been postulated for how increased physical activity, such as strenuous work, could lead to adverse outcomes of pregnancy (16, 17). Clapp (17) summarized the physiological changes that occur during physical activity: cardiac output is redistributed from visceral circulation to exercising muscles and skin, energy stores are depleted, body temperature increases, the hormonal milieu abruptly changes and a variety of physical stresses occur, all of which are intensified by either increasing the workload or length of the physical activity. These changes have the potential to adversely affect the course and outcome of pregnancy (e.g., infertility, abortion, congenital malformation, cord entanglement, placental separation, membrane rupture, growth restriction, premature labor or fetal hypoxia). Most of these adverse outcomes have been identified in animal models, and two (premature labor, fetal growth restriction) were found in humans in association with physical activity in the workplace (17).
Interestingly, the biological mechanisms underlying an association between strenuous work during pregnancy and adverse reproductive outcome usually do not include nutritional explanations per se. Explanations have focused on increased sympathetic vasomotor tone to skeletal muscles, decreased plasma volume resulting from prolonged standing, catecholamine release resulting in increased uterine vasoconstriction and hyperthermia (18). Findings support the notion that increased physical activity may be beneficial to the outcome of pregnancy. For example, women who exercise during pregnancy have been observed to have a lower risk of spontaneous abortion (19).
Thus, making an inference that physical or strenuous activity in the workplace contributes to the etiology of adverse reproductive outcomes is complicated by the observation that increased physical activity during pregnancy is likely to be beneficial relative to some pregnancy outcomes. However, the factual basis of that statement can be questioned. For example, a recent study from Denmark indicated that physical activity peaks at critical times (specifically implantation) were associated with an increase in spontaneous abortion (20). This finding is consistent with an alternative interpretation (21).
Physical exertion in the workplace during pregnancy may be predictive of adverse reproductive outcome. Particular occupations, long hours on the job, irregular hours and shift work have been implicated (22 24). Many studies have suggested that strenuous physical activity, including in the workplace during pregnancy, is associated with reduced infant birth weight, lower pregnancy weight gain, shorter gestations, intrauterine growth retardation, spontaneous abortions, fecundity and some congenital malformations (12, 13, 25 42). These types of associations, however, have not been observed in other studies (18, 43 48). Moreover, only a few such studies have been conducted in developing countries (25 28, 40).
This fairly sizable literature was recently reviewed (49, 50). Numerous methodological differences and explanations likely contribute to the inconsistency of observed results, including variability in the definition of strenuous work activities (e.g., prolonged standing, lifting, working long hours and higher energy expenditures), lack of information on potential confounders, lack of information on actual workplace exposures and failure of most studies to consider the additional potential effects of physical demands outside the workplace.
The literature also reveals some other interesting associations. Women with high-stress jobs, defined as jobs high in demands and low in control, have been observed to deliver babies weighing 190 g less than women who had low-stress jobs or were unemployed (51). Such high-stress jobs have been associated with other pregnancy outcomes as well, such as preeclampsia (52). Thus, to adequately consider potential pregnancy effects of strenuous activity in the workplace, the psychological stress component of women's jobs needs to be considered.
Nutritional deficiencies, compromised or lowered intakes and adverse reproductive outcomes: epidemiologic evidence
Data from developing countries on this topic are limited. Women from one region in Africa with chronic energy deficiency (defined as a body mass index, calculated as kg/m2, of <18.5) were more likely to have a lower male-to-female ratio for offspring (fewer male births) than were women with higher body mass indexes. Short stature and obesity both contributed to the lowered sex ratio (53).
Epidemiologic data indicate that periconceptional vitamin supplementation substantially reduces the risk for neural tube defects, orofacial clefts, selected heart malformations and other congenital malformations (54 56). This risk reduction may be specifically attributable to folic acid supplementation (57) but is unlikely to be explained by a simple maternal vitamin deficiency or a simple maternal absorption deficiency (58). Evidence points toward disordered folate metabolism in some susceptible individuals, with the metabolic error affecting uptake or metabolism of folate by fetal cells (59). Several epidemiologic studies also investigated the influence of folic acid and multivitamin supplement intake on the occurrences of other reproductive outcomes, such as low birth weight and preterm delivery (60 62).
Nutritional factors other than folic acid have also been observed to influence risks of congenital malformations (63 65). For example, increased intakes of methionine (66), zinc (67), vitamin C (68) and dairy products (69) have been associated with decreased risk for neural tube defects. Maternal factors such as diabetes (70), prepregnancy obesity (71), hyperinsulinemia (72) and intakes of sweets (73) also have been associated with increased risks.
Conclusion
The available data are insufficient to draw firm inferences that strenuous work, in either a developing country or a developed country, alters a pregnant woman's nutritional status and therefore affects her risk of an adverse pregnancy outcome. Effects on the nutritional status, micronutrients in particular, of pregnant women from strenuous physical activities at work or in other lifestyle events require further study in developing countries. In addition, how nutritional status effects might influence risks of adverse reproductive outcomes also requires further study, particularly in developing countries.
| FOOTNOTES |
|---|
2 This research was partially supported by funds from the Centers for Disease Control and Prevention, Centers of Excellence Award No. U50/CCU913241. ![]()
| LITERATURE CITED |
|---|
|
|
|---|
1. Prentice, A. M., Whitehead, R. G., Watkinson, M., Lamb, W. H. & Cole, T. J. (1983) Prenatal dietary supplementation of African women and birth-weight. Lancet 5: 489491.
2. Prentice, A. M., Cole, T. J., Foord, F. A., Lamb, W. H. & Whitehead, R. G. (1987) Increased birthweight after prenatal dietary supplementation of rural African women. Am. J. Clin. Nutr. 46: 912925.
3. Ceesay, S. M., Prentice, A. M., Cole, T. J., Foord, F., Weaver, L. T., Poskitt, E. M. & Whitehead, R. G. (1997) Effects on birthweight and perinatal mortality of maternal dietary supplements in rural Gambia: 5 year randomised controlled trial. BMJ 315: 786790.
4. Rao, S., Kanade, A., Margetts, B. M., Yajnik, C. S., Lubree, H., Regee, S., Desai, B., Jackson, A. & Fall, C. H. D. Maternal activity in relation to birth size in rural India: The Pune Maternal Nutrition Study. Br. J. Nutr., in press.
5. Torun, B., McGuire, J. & Mendoza, R. D. (1982) Energy cost of activities and tasks of women from a rural region of Guatemala. Nutr. Res. 2: 127136.
6. Norgan, N. G., Ferro-Luzzi, A. & Durnin, V. G. A. (1974) The energy and nutrient intake and the energy expenditure of 204 New Guinean adults. Philos. Trans. R. Soc. Lond. B Biol. Sci. 268: 309348.[Medline]
7. Bleiberg, F. M., Brun, T. A. & Goihman, S. (1980) Duration of activities and energy expenditure of female farmers in dry and rainy seasons in Upper-Volta. Br. J. Nutr. 43: 7182.[Medline]
8. Lawrence, M., Singh, J., Lawrence, F. & Whitehead, R. G. (1985) The energy cost of common daily activities in African women: increased expenditure in pregnancy. Am. J. Clin. Nutr. 42: 753763.
9. Banerjee, B., Khew, K. S. & Saha, N. (1971) A comparative study of energy expenditure in some common daily activities of non-pregnant and pregnant Chinese, Malay, and Indian women. J. Obstet. Gynaecol. Br. Commonw. 78: 113116.[Medline]
10. Bendich, A. (1993) Lifestyle and environmental factors that can adversely affect maternal nutritional status and pregnancy outcomes. In: Maternal nutrition and pregnancy outcome (Keen, C., Bendich, A. & Wilhite, C., eds.), pp. 255265. New York Acad. Sci., New York, NY.
11. Zuckerman, B. S., Frank, D. A., Hingson, R., Morelock, S. & Kayne, H. L. (1986) Impact of maternal work outside the home during pregnancy on neonatal outcome. Pediatrics. 77: 459464.
12. Eskenazi, B., Fenster, L., Wight, S., English, P., Windham, G. C. & Swan, S. H. (1994) Physical exertion as a risk factor for spontaneous abortion. Epidemiology 5: 613.[Medline]
13. Hatch, M., Ji, B.-T., Shu, X. O. & Susser, M. (1997) Do standing, lifting, climbing, or long hours have an effect on fetal growth? Epidemiology 8: 530536.[Medline]
14. Wergeland, E. & Strand, K. (1998) Work pace control and pregnancy health in a population-based sample of employed women in Norway. Scand. J. Work Environ. Health 45: 581588.
15. Clapp, J. F., III, Kim, H., Burciu, B., Schmidt, S., Petry, K. & Lopez, B. (2002) Continuing regular exercise during pregnancy: effect of exercise volume on fetoplacental growth. Am. J. Obstet. Gynecol. 186: 142147.[Medline]
16. Huch, R. & Erkkola, R. (1990) Pregnancy and exercise exercise and pregnancy. A short review. Br. J. Obstet. Gynaecol. 97: 208214.[Medline]
17. Clapp, J. F., Iii. (1996) Pregnancy outcome: physical activities inside versus outside the workplace. Semin. Perinatol. 20: 7076.[Medline]
18. Simpson, J. L. (1993) Are physical activity and employment related to preterm birth and loew birth weight? Am. J. Obstet. Gynecol. 168: 12311238.[Medline]
19. Latka, M., Kline, J. & Hatch, M. (1999) Exercise and spontaneous abortion of known karotype. Epidemiology 10: 7375.[Medline]
20. Hjollund, N. H., Jensen, T. K., Bonde, J. P., Henriksen, T. B., Andersson, A. M., Kolstad, H. A., Ernst, E., Giwercman, A., Skakkebaek, N. E. & Olsen, J. (2000) Spontaneous abortion and physical strain around implantation: a follow-up study of first pregnancy planners. Epidemiology 11: 1823.[Medline]
21. Hatch, M. (2000) Physical activity before you know you are pregnant. Epidemiology 11: 45.[Medline]
22. Axellson, G., Rylander, R. & Molin, I. (1989) Outcome of pregnancy in relation to irregular and inconvenient work schedules. Br. J. Ind. Med. 46: 196199.[Medline]
23. Mamelle, N., Laumon, B. & Lazar, P. (1984) Prematurity and occupational activity during pregnancy. Am. J. Epidemiol. 119: 309322.
24. Armstrong, B. G., Nolin, A. D. & McDonald, A. D. (1989) Work in pregnancy and birthweight for gestational age. Br. J. Ind. Med. 46: 196199.
25. Tafari, N., Naeye, R. L. & Gobezie, A. (1980) Effects of maternal undernutrition and heavy physical work during pregnancy on birth weight. Br. J. Obstet. Gynaecol. 87: 222226.[Medline]
26. Tan, T. C., Donnan, S. P. & Chang, A. M. (1998) Employment, physical overactivity and adverse pregnancy outcomesapplicability of AMA guidelines in Chinese women. Asia Pac. J. Public Health 2: 2227.
27. Barnes, D. L., Adair, L. S. & Popkin, B. M. (1999) Women's physical activity and pregnancy outcome: a longitudinal analysis from the Philippines. Int. J. Epidemiol. 20: 162172.
28. Tuntiserance, P., Geater, A., Chongsuvivatwong, V. & Kor-Anantakul, O. (1998) The effect of heavy maternal workload on fetal growth retardation and preterm delivery. J. Occup. Environ. Med. 40: 10131020.[Medline]
29. Clapp, J. F. & Dichstein, S. (1984) Endurance exercise and pregnancy outcome. Med. Sci. Sports Exerc. 16: 556562.[Medline]
30. Fox, M. E., Harris, R. E. & Brekken, A. L. (1977) The active-duty military pregnancy. A new high-risk category. Am. J. Obstet. Gynecol. 129: 705707.[Medline]
31. Naeye, R. L. & Peters, E. (1982) Working during pregnancy: Effects on the fetus. Pediatrics 69: 724727.
32. McDonald, A. D., McDonald, J. C., Armstrong, B., Cherry, N. M., Cote, R., Lavoie, J., Nolin, A. D. & Robert, D. (1988) Congenital defects and work in pregnancy. Br. J. Ind. Med. 45: 581588.[Medline]
33. Marcoux, S., Brisson, J. & Fabia, J. (1989) The effect of leisure time physical activity on the risk of pre-eclamsia and gestational hypertension. J. Epidemiol. Community Health 43: 147152.
34. Florack, E. I. M., Zielhuis, G. A., Pellegrino, J. E. & Rolland, R. (1993) Occupational physical activity and the occurrence of spontaneous abortion. Int. J. Epidemiol. 22: 878884.
35. Florack, E. I. M., Zielhuis, G. A. & Rolland, R. (1994) The influence of occupational physical activity on the menstrual cycle and fecundability. Epidemiology 5: 1418.[Medline]
36. Klebanoff, M. A., Shiono, P. H. & Rhoads, G. G. (1990) Outcomes of pregnancy in a national sample of resident physicians. N. Engl. J. Med. 323: 10401045.[Abstract]
37. Ahlborg, G. (1995) Physical work load and pregnancy outcome. J. Occup. Environ. Med. 37: 941944.[Medline]
38. Spinillo, A., Capuzzo, E., Baltro, F., Baltaro, F., Piazzi, G., Nicola, S. & Iasci, A. (1996) The effect of work activity in pregnancy on the risk of fetal growth retardation. Acta Obstet. Gynecol. Scand. 75: 531536.[Medline]
39. Spinillo, A., Capuzzo, E., Colonna, L., Piazzi, G., Nicola, S. & Baltaro, F. (1995) The effect of work activity in pregnancy on the risk of severe pre-eclampsia. Aust. N. Z. J. Obstet. Gynaecol. 35: 380385.[Medline]
40. Ceron-Mireles, P., Harlow, S. D. & Sanchez-Carillo, C. I. (1996) The risk of prematurity and small-for-gestational-age birth in Mexico City: The effects of working conditions and antenatal leave. Am. J. Public Health 86: 825831.
41. Lin, S., Gensburg, L., Marshall, E. G., Roth, G. B. & Dlugosz, L. (1998) Effects of maternal work activity during pregnancy on infant malformations. J. Occup. Environ. Med. 40: 829834.[Medline]
42. Launer, L. J., Villar, J., Kestler, E. & de Onis, M. (1981) The effect of maternal work on fetal growth and duration of pregnancy: a prospective study. Br. J. Obstet. Gynaecol. 97: 6270.
43. Berkowitz, G. S. (1981) An epidemiologic study of preterm delivery. Am. J. Epidemiol. 131: 8192.
44. Hall, D. C. & Kaufman, D. A. (1987) Effects of aerobic and strength conditioning on pregnancy outcomes. Am. J. Obstet. Gynecol. 157: 11991203.[Medline]
45. Lokey, E. A., Tran, Z. V., Wells, C. L., Myers, B. C. & Tran, A. C. (1991) Effects of physical exercise on pregnancy outcomes: a meta-analytic review. Med. Sci. Sports Exerc. 23: 12341239.[Medline]
46. Irwin, D. E., Savitz, D. A., St Andre, K. & Hertz-Picciotto, I. (1994) Study of occupational risk factors for pregnancy-induced hypertension among active duty enlisted Navy personnel. Am. J. Ind. Med. 25: 349359.[Medline]
47. Magann, E. F., Evans, S. F. & Newnham, J. P. (1996) Employment, exertion, and pregnancy outcome: Assessment by kilocalories expended each day. Am. J. Obstet. Gynecol. 175: 182187.[Medline]
48. Fenster, L., Hubbard, A. E., Windham, G. C., Waller, K. O. & Swan, S. H. (1997) A prospective study of work-related physical exertion and spontaneous abortion. Epidemiology 8: 6674.[Medline]
49. Gabbe, S. G. & Turner, L. P. (1997) Reproduction hazards of the American lifestyle: work during pregnancy. Am. J. Obstet. Gynecol. 176: 826832.[Medline]
50. Pivarnik, J. M. (1998) Potential effects of maternal physical activity on birthweight: brief review. Med. Sci. Sports Exerc. 30: 400406.[Medline]
51. Oths, K. S., Dunn, L. L. & Palmer, N. S. (2001) A prospective study of psychosocial job strain and birth outcomes. Epidemiology 12: 744746.[Medline]
52. Klonoff-Cohen, H. S., Cross, J. L. & Pieper, C. F. (1996) Job stress and pre-eclampsia. Epidemiology 7: 245249.[Medline]
53. Andersson, R. & Berstrom, S. (1998) Is maternal malnutrition associated with a low sex ratio at birth? Hum. Biol. 70: 11011106.[Medline]
54. Medical Research Council Vitamin Study Research Group. (1991) Prevention of neural tube defects: results of the Medical Research Council vitamin study. Lancet 338: 131137.[Medline]
55. Shaw, G. M., Lammer, E. J., Wasserman, C. R., O'Malley, C. D. & Tolarova, M. M. (1995) Risks of orofacial clefts in children born to women using multivitamins containing folic acid periconceptionally. Lancet 345: 393396.
56. Shaw, G. M., O'Malley, C. D., Wasserman, C. R., Tolarova, M. M. & Lammer, E. J. (1995) Maternal periconceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring. Am. J. Med. Genet. 59: 536545.[Medline]
57. Berry, R. J. & Li, Z. (2002) Folic acid alone prevents neural tube defects: evidence from the China study. Epidemiology 13: 114116.[Medline]
58. Bower, C., Stanley, F. J., Croft, M., de Klerk, N., Davis, R. E. & Nicol, D. J. (1993) Absorption of pterolpolyglutamates in mothers in infants with neural tube defects. Br. J. Nutr. 69: 827834.[Medline]
59. Botto, L. D. & Yang, Q. (2000) 5,10methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review. Am. J. Epidemiol. 151: 862877.
60. Scholl, T. O., Hediger, M. L., Bendich, A., Schall, J. I., Smith, W. K. & Krueger, P. M. (1997) Use of multivitamin/mineral prenatal supplements: influence on the outcome of pregnancy. Am. J. Epidemiol. 146: 134141.
61. Shaw, G. M., Liberman, R. F., Todoroff, K. & Wasserman, C. R. (1997) Low birth weight, preterm delivery, and periconceptional vitamin use. J. Pediatr. 130: 10131014.
62. Mathews, F., Yudkin, P. & Neil, A. (1999) Influence of maternal nutrition on outcome of pregnancy: prospective cohort study. BMJ 319: 339343.
63. Sharma, R. P. (1993) Dietary factors and birth defects. Pacific Div. Am. Assn. Adv. Sci. San Francisco, CA.
64. Pitt, D. B. & Samson, P. E. (1961) Congenital malformations and maternal diet. Australas. Ann. Med. 10: 268274.[Medline]
65. Rothman, K. J., Moore, L. L., Singer, M. R., Nguyen, U. S., Mannino, S. & Milunsky, A. (1995) Teratogenicity of high vitamin A intake. N. Engl. J. Med. 333: 13691373.
66. Shaw, G. M., Velie, E. M. & Schaffer, D. (1997) Is dietary intake of methionine associated with a reduction in risk for neural tube defect-affected pregnancies? Teratology 56: 295299.[Medline]
67. Velie, E. M., Block, G., Shaw, G. M., Samuels, J., Schaffer, D. M. & Kuldorff, M. (1999) Maternal supplemental and dietary zinc intake and the occurrence of neural tube defects in California. Am. J. Epidemiol. 150: 605616.
68. Schorah, C. J., Wild, J., Hartley, R., Sheppard, S. & Smithells, R. W. (1983) The effect of periconceptional supplementation on blood vitamin concentrations in women at recurrence risk for neural tube defect. Br. J. Nutr. 49: 203211.[Medline]
69. Shaw, G. M., Todoroff, K., Schaffer, D. M. & Selvin, S. (1999) Periconceptional nutrient intake and risk for neural tube defect-affected pregnancies. Epidemiology 10: 711716.[Medline]
70. Becerra, J. E., Khoury, M. J., Cordero, J. F. & Erickson, J. D. (1990) Diabetes mellitus during pregnancy and the risks for specific birth defects: a population-based case-control study. Pediatrics 85: 19.
71. Shaw, G. M., Velie, E. M. & Schaffer, D. (1996) Risk of neural tube defect-affected pregnancies among obese women. JAMA 275: 10931096.
72. Hendricks, K. A., Nuno, O. M., Suarez, L. & Larsen, R. (2001) Effects of hyperinsulinemia and obesity on risk of neural tube defects among Mexican Americans. Epidemiology 12: 630635.[Medline]
73. Friel, J. K., Frecker, M. & Fraser, F. C. (1995) Nutritional patterns of mothers of children with neural tube defects in Newfoundland. Am. J. Hum. Genet. 55: 195199.
This article has been cited by other articles:
![]() |
I. M. Mogren Previous physical activity decreases the risk of low back pain and pelvic pain during pregnancy Scand J Public Health, August 1, 2005; 33(4): 300 - 306. [Abstract] [PDF] |
||||
![]() |
A. A. Jackson, Z. A. Bhutta, and P. Lumbiganon Introduction J. Nutr., May 1, 2003; 133(5): 1589S - 1591. [Full Text] [PDF] |
||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||