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Placenta: a possible predictor of vitamin A deficiency

Published online by Cambridge University Press:  15 December 2009

Mirian Martins Gomes*
Affiliation:
Nucleus of Micronutrient Research – Josué de Castro Institute – Federal University of Rio de Janeiro, Rio de Janeiro, Brazil Oswaldo Cruz Foundation, Fernandes Figueira Institute, Avenida Paulo de Frontin, 451/609, CEP 20261-240, Rio Comprido-Rio de Janeiro, RJ, Brazil
Claudia Saunders
Affiliation:
Nucleus of Micronutrient Research – Federal University of Rio de Janeiro, Josué de Castro Institute, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil Edifício dos Institutos Bloco J, 2°. andar, Instituto de Nutrição Josué de Castro, Departamento de Nutrição e Dietética, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, CEP 21.941.590, Rio de Janeiro, RJ, Brazil
Andrea Ramalho
Affiliation:
Nucleus of Micronutrient Research – Federal University of Rio de Janeiro, Josué de Castro Institute, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil Edifício dos Institutos Bloco J, 2°. andar, Instituto de Nutrição Josué de Castro, Departamento de Nutrição e Dietética, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, CEP 21.941.590, Rio de Janeiro, RJ, Brazil
*
*Corresponding author: Mirian Martins Gomes, fax +55 21 25541925, email [email protected]
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Abstract

The objective of the present study is to assess the association between vitamin A deficiency (VAD) evaluated by serum retinol concentration from the mother and umbilical cord and placental concentration of retinol and carotenoids to propose placental values representative of deficiency. Two hundred and sixty-two puerperal women and their newborns were assessed. Concentration of serum and placental retinol and carotenoids was determined by the spectrophotometric method. Receiver operating characteristic (ROC) curve analysis was performed according to two cut-off points (0·70 and 1·05 μmol/l) to represent deficiency in the placental concentration. No difference between averages of placental retinol and carotenoids was observed in the puerperal women regardless of the cut-off point used to define VAD. In relation to the newborns, a decrease (P = 0·012) in placental retinol averages in individuals with VAD was observed when the 1·05 μmol/l cut-off point was adopted. In respect to the placental carotenoid averages, a decrease is observed for both the cut-off points (P = 0·013 and 0·019 for 1·05 and 0·7 μmol/l, respectively). The ROC curve results point to the value of 0·80 μmol/l as representing deficiency with greater values found for sensitivity (66·7 %), specificity (41·7 %) and accuracy (65 %) when the 0·70 μmol/l cut-off point was adopted. The results of the present study show an association between the placental concentration of retinol and carotenoids with clinical VAD, suggesting the need for further studies on more severe cases of deficiency.

Type
Full Papers
Copyright
Copyright © The Authors 2009

Vitamin A deficiency (VAD) is a public health problem of paramount relevance. Its growing prevalence has been warned since the 1990s(Reference Ferraz, Daneluzzi and Annucchi1Reference Sommer5).

Vitamin A is vital during the initial stages of life. Its role goes beyond embryonic development, tissue homeostasis, lipid metabolism and cellular differentiation and proliferation. Human placentae express factors for the nuclear transcription of retinoic acid receptors and retinoic X receptors. Modulation of these factors by retinoic acid is capable of modulating the expression of several genes such as: chorionic gonadotrophic hormone; placental lactogenic hormone; leptin; epidermal growth factor receptor; triiodothyronine; oestrogen; progesterone; cortisol; aldosterone; testosterone; vitamin D; cholesterol; fatty acids(Reference Sarni, Kochi and Ramalho7Reference Burri9).

In 1996, the WHO underscored the need for proposed guidelines on proper selection, use and interpretation of indicators, not just to map deficiency but also to propose programmes to assess the impact of interventions to control VAD.

The placenta is the only organ composed of cells from two distinct individuals(Reference Iyengar and Rapp10). So far, no studies have been done to evaluate retinol and carotenoid concentration in the placenta and its relation with the nutritional state of the mother and the child. Some authors describe the presence of receptors for the vitamin in the brush border membrane of the placenta, implying that the placenta may have a regulatory mechanism(Reference Barnes11Reference Sundaram, Sivaprasadarao and De Sousa13).

In this scenario, the objective of the present study was to evaluate the association between serum and placental concentration of vitamin A and to propose values of placental retinol representing VAD.

Methodology

Population and sample

The population studied was made up of low-risk puerperal women, who received antenatal care services at the maternity hospital of the Universidade Federal do Rio de Janeiro, being 262 women chosen according to the following criteria: single-child pregnancy; absence of clinically proven pathologies identified before gestation (diabetes mellitus and liver, heart or kidney diseases) or no use of vitamin–mineral supplementation containing vitamin A during gestation.

Collection and analysis of placenta samples

Obtaining the placentae as well as their weighing were performed immediately postpartum after separation of the newborn(Reference Thomson, Billewicz and Hytten14, Reference Saunders, Leal and Flores15). Before obtaining placentae samples, the amniochorionic membrane and the umbilical cord were separated. The collection was carried out by using a surgical scalpel in a dimly lit environment(Reference Saunders, Leal and Flores15, Reference Barreto-Lins, Campos and Azevedo16). Treatment, storage and transportation of the samples were carried out according to procedures described by Saunders et al. (Reference Saunders, Leal and Flores15).

Biochemical evaluation of vitamin A nutritional status

To determine the concentration of maternal and cord blood retinol and total carotenoids, 5-ml samples of blood were collected intravenously from the puerperal women fasting for 8 h, as well as from the newborns' umbilical cord immediately postpartum(Reference Saunders, Leal and Flores15, Reference Ramalho, Anjos and Flores17). The blood samples obtained were centrifuged (3000 rpm) to separate and extract the serum and were immediately frozen at a temperature of − 20°C at the laboratory of the ME/UFRJ. Thereafter, all the samples were packaged in order to guarantee that the temperature was maintained during transportation to the INJC/UFRJ, where they were kept frozen until the moment the retinol and carotenoids concentration was analysed at the Institution's Biochemical Laboratory.

Biochemical quantification

Determination of serum retinol and carotenoid concentration was performed through spectrophotometric analysis based on the Bessey et al. (Reference Bessey, Lowry and Brock18) method modified by Araujo & Flores(Reference Araújo and Flores19) and in accordance with procedures adopted by Flores et al. (Reference Flores, Ramalho and Ribeiro20) for dosing the hepatic vitamin A. All the samples were analysed in duplicate, following the precautionary measures recommended by the International Vitamin A Consultative Group, in order to assure sample quality before analysis(Reference Barreto-Lins, Campos and Azevedo16, Reference Arroyave, Chichester and Flores21). For a sample of nine placental portions, vitamin A concentration was also determined by HPLC(Reference Hess, Keller and Oberlin22).

Cut-off points of 0·7 and 1·05 μmol/l were adopted to indicate VAD(Reference Christian, West and Khatry2326). To indicate carotenoid insufficiency, cut-off points of < 800 μg/l for the puerperal women(Reference Sauberlich, Apud Oliveira and Marchini27) and < 400 μg/l for the newborns(Reference Sauberlich, Apud Oliveira and Marchini27, Reference Robles-Sardin, Astiazarán-Gracia and Dávalos-Navarro28) were adopted.

Treatment of statistics

Outlier retinol values (defined as mean ± 3 sd) were identified in two blood and seven placenta samples. All the samples originated from the blood and placentae in which these extreme values detected were excluded from the final analysis.

The Student t test was used to compare means. The log transformation was used to approximate variables to the normal distribution. The paired t test was used to compare biochemical methods. The receiver operating characteristic curve was used to establish the placental retinol and carotenoid concentration representative of their serum concentration through sensitivity and specificity evaluation for each cut-off point. The best optimal point was determined to be the one, which maximised the sensitivity and specificity values. The level of significance established was P < 0·05. Statistical analysis was performed using the statistical program SPSS for Windows version 15.0 (SPSS, Chicago, IL, USA).

Ethical issues

The study was carried out through an institutional accord between the Nucleus of Micronutrient Research of Josué de Castro Institute of Federal University of Rio de Janeiro (NPqM/INJC/UFRJ) and the maternity hospital (ME/UFRJ). Data collection took place after approval by the ethics commission of the said maternity school and the ethics committee of the Escola Nacional de Saúde Pública of Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.

Results

The puerperal participants in the study were on average of 26 (sd 5·8) years old, presented an average pre-pregnancy weight of 55·2 (sd 9) kg and total weight gain of 12·9 (sd 5·7) kg. Their newborns presented birth weights of 3·27 (sd 0·45) kg and the placentae weighed on average of 0·640 (sd 0·144) kg. Gestational duration was 39 (sd 1·6) weeks.

According to the results shown in Tables 1 and 2, a decrease in concentration in placental retinol within the VAD margins was observed for both the mother and the newborn, regardless of the cut-off point adopted.

Table 1 Placental retinol and total carotenoid averages according to maternal and newborn vitamin A nutritional state

(Mean values and standard deviations)

VAD, vitamin A deficiency.

Placental retinol and total carotenoids means were compared according to vitamin A status classified by serum retinol cut-off points (1·05 and 0·70 μmol/l) for mother and newborn. Vitamin A status was defined as VAD and normal according to each cut-off point. Placental retinol and total carotenoids means were then calculated for each group.

Table 2 Comparison of placental retinol and total carotenoid averages after logn transformation according to maternal and newborn vitamin A nutritional state

(Mean values and standard deviations are presented as logn transformation)

VAD, vitamin A deficiency.

Placental retinol and total carotenoids means were compared according to vitamin A status classified by serum retinol cut-off points (1·05 and 0·70 μmol/l) for mother and newborn. Vitamin A status was defined as VAD and normal according to each cut-off point. Placental retinol and total carotenoids means were then calculated for each group.

Regarding carotenoids, the drop was also observed in newborns as there is a statistically significant difference between the placental carotenoid averages regardless of the cut-off point.

Analysis of the receiver operating characteristic curve was carried out for the placental concentrations of retinol according to the two cut-off points for classifying VAD both for the mother and the newborn. Values for the placental concentrations of retinol of < 0·80 μmol/l were adopted as predictors of inadequate serum concentration according to values of specificity, sensitivity and the area under the curve (accuracy) (Table 3) presented. It was observed that sensitivity increases as the cut-off point for serum concentrations is lowered, in other words, as the VAD is aggravated. Additionally, regardless of the cut-off point adopted to classify serum concentration of retinol, the sensitivity and specificity results show increases in the newborn when compared with the puerperal woman. The best accuracy value (65 %) was found for the curve made from the second 0·70 μmol/l cut-off point to identify puerperal deficiency.

Table 3 Sensitivity and specificity results according to serum cut-off points for vitamin A deficiency adopting the placental cut-off point 0·80 μmol/l according to analysis of the receiver operating characteristic curve

A receiver operating characteristic curve taken from the placental concentrations of carotenoids did not permit the adoption of any value that could represent their serum inadequacy.

No difference was found between the values obtained in retinol concentration with the spectrophotometric and with the HPLC analytical methods (P = 0·318). The spectrophotometric method may be an alternative when HPLC is not available.

Discussion

The placenta is able to esterify retinoid and produce active retinoid by means of retinol, thus allowing it to produce the active metabolites it needs(Reference Marceau, Gallot and Borel6). The present study aims to evaluate the association between serum and placental concentration of vitamin A and propose a placental retinol value representing VAD.

An association between average concentrations of total placental carotenoids according to fetal nutritional states of vitamin A was found. Although the analysis of the receiver operating characteristic curve from the placental retinol concentration has shown not to predict sub-clinical deficiency, it was noted that sensitivity and specificity values increased when the cut-off point was lowered from 1·05 to 0·70 μmol/l. This fact may be interpreted as the placental vitamin A content being more related to a severer state of VAD.

In this sense, evaluation of the curve with the cut-off points at different stages of severity of the deficiency illness in question is necessary. Such an approach was not carried out in the present study, due to the fact that there were not a large enough number of grave VAD cases (according to the WHO's cut-off points, 1996)(26) to create the curve. The same phenomenon was also noted for sensitivity and specificity values when comparing puerperal women and newborns, the results tend to be more expressive in the newborns.

In states of privation, retinol is the priority ahead of provitamin A carotenoids, being the latter converted to vitamin A as needed. It is known that the enzyme β-carotene 15,15′-monooxygenase, responsible for splitting the β-carotene molecules into two retinal molecules, is present in the fetal part of the amniotic membrane of the human placenta(Reference Marceau, Gallot and Borel6, Reference Morriss-Kay and Sokolova29). This fact may account for the better association of placental concentrations with the serum concentrations of newborns, besides justifying the difficulty in finding placental concentrations of carotenoids to represent both the maternal and the newborn serum concentrations.

The placenta appears to be a possible indicator of vitamin A status for women and their newborns and could be used to determine the prevalence of VAD. On the other hand, during the puerperal period, the greatest transfer of vitamin A to the neonate takes place through breastfeeding. Thus, this organ may also contribute to the development of treatment strategies to prevent transmission of the afore-mentioned deficiency.

The results of the present study point to an association between vitamin A nutritional state and the placental concentrations of retinol and carotenoids. The present study using the placenta as a marker for VAD suggests the need for further studies to assess additional cut-off points for severe privation and to define cut-off points for the placental concentrations.

Although spectrophotometric method is not the best for vitamin A dosing, the present study analysed a sub-sample with both the spectrophotometric and the HPLC methods. Spectrophotometrics seemed to be an alternative method when HPLC is not available. Unfortunately this analysis could not cater for all the cases studied. So we recommend further studies on this topic.

Acknowledgements

The authors want to express their gratitude to: the researchers and volunteers who participated in the present study; the Board of directors of the maternity hospital of Universidade Federal do Rio de Janeiro that made the study possible; the Conselho Nacional de Desenvolvimento Científico e Tecnológico – CNPq; the Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro Carlos Chagas Filho – FAPERJ; the Secretaria Estadual de Saúde do Rio de Janeiro for financial support. M. M. G. participated in data collection and analyses; C. S. supervised the fieldwork and data collection and participated in study design; A. R. participated in study design. All the authors participated in manuscript preparation. None of the authors had a personal or financial interest to declare.

References

1 Ferraz, IS, Daneluzzi, JC, Annucchi, H, et al. (2005) Prevalência da carência de ferro e sua associação com a deficiência de vitamina A em pré-escolares (Prevalence of iron deficiency and its association with vitamin A deficiency in preschool children). J Pediatr (Rio J) 81, 169174.CrossRefGoogle Scholar
2 West, KP Jr (2002) Extent of vitamin A deficiency among preschool children and women of reproductive age. J Nutr 132, 2857S2866S.CrossRefGoogle ScholarPubMed
3 Maison, JB, Lotfi, M, Dalmiya, N, et al. (2001) The Micronutrient Report. Current Progress and Trends in the Control of Vitamin A, Iodine, and Iron Deficiencies. Ottawa: The Micronutrient Initiative/UNICEF.Google Scholar
4 World Health Organization (1999) Reducción de la mortalidad materna. Declaración conjunta OMS/FNUAP/UNICEF/Banco Mundial (Reduction of Maternal Mortality. Joint Declaration of OMS/FNUAP/UNICEF/World Bank). Geneva: WHO. (Classificación NLM:HB 1322·5).Google Scholar
5 Sommer, A (1995) La carencia de vitamina A y sus consecuencias. Guía práctica para la detección y el tratamiento (Vitamin A Deficiency and Its Consequences. Practical Guide for Detection and Treatment), Tercera edición. Geneva: WHO.Google Scholar
6 Marceau, G, Gallot, D, Borel, V, et al. (2006) Molecular and metabolic retinoid pathway in human amniotic membranes. Biochem Biophys Res Commun 346, 12071216.CrossRefGoogle ScholarPubMed
7 Sarni, RS, Kochi, C, Ramalho, RA, et al. (2002) Vitamina A: nível sérico e ingestão dietética em crianças e adolescentes com déficit estatural de causa não hormonal (Vitamin A: blood level and dietary intake in children and adolescents with short stature not hormonally caused). Rev Assoc Med Bras 48, 4853.CrossRefGoogle Scholar
8 Radhika, MS, Bhaskaram, P, Balakrishma, N, et al. (2002) Effects of vitamin A deficiency during pregnancy on maternal and child health. Int J Gynaecol Obstet 109, 689693.CrossRefGoogle ScholarPubMed
9 Burri, BJ (2002) The formation of vitamin A from β-carotene: good, bad and variable. Sight and Life Newsletter no. 2.Google Scholar
10 Iyengar, GV & Rapp, A (2001) Human placenta as a ‘dual’ biomarker for monitoring fetal and maternal environment with special reference to potentially toxic trace elements. Part 1: physiology, function and sampling of placenta for elemental characterization. Sci Total Environ 280, 195206.CrossRefGoogle Scholar
11 Barnes, AC (1951) The placental metabolism of vitamin A. Am J Obstet Gynecol 61, 368372.CrossRefGoogle ScholarPubMed
12 Dimenstein, R, Trugo, NMF, Donangelo, CM, et al. (1996) Effect of subadequate maternal vitamin A status on placental transfer of retinol and beta-carotene to the human fetus. Biol Neonate 69, 230234.CrossRefGoogle Scholar
13 Sundaram, M, Sivaprasadarao, A, De Sousa, MM, et al. (1998) The transfer of retinol from serum retinol-binding protein to cellular retinol-binding protein is mediated by a membrane receptor. J Biol Chem 273, 33363342.CrossRefGoogle ScholarPubMed
14 Thomson, AM, Billewicz, WZ & Hytten, FE (1969) The weight of the placenta in relation to birth weight. J Obstet Gynaecol Br Commonw 76, 865872.CrossRefGoogle Scholar
15 Saunders, C, Leal, MC, Flores, H, et al. (2005) Intraplacental distribution of retinol. Int J Food Sci Nutr 56, 607612.CrossRefGoogle ScholarPubMed
16 Barreto-Lins, MHC, Campos, FACS & Azevedo, MNA (1988) A re-examination of the stability of retinol in blood and serum, and effects of standardized meal. Clin Chem 34, 28082810.CrossRefGoogle ScholarPubMed
17 Ramalho, RA, Anjos, LA & Flores, H (1999) Estado nutricional de vitamina A no binômio mãe/recém-nascido em duas maternidades no Rio de Janeiro, Brasil (Nutritional status of vitamin A in mother/newborn in two hospitals in Rio de Janeiro, Brazil). Arch Latinoam Nutr 49, 318321.Google Scholar
18 Bessey, OA, Lowry, OH, Brock, MJ, et al. (1946) The determination of vitamin A and carotene in small quantities of blood serum. J Biol Chem 1, 177188.CrossRefGoogle Scholar
19 Araújo, CRC & Flores, H (1978) Improved spectrophotometric vitamin A assay. Clin Chem 24, 386.CrossRefGoogle ScholarPubMed
20 Flores, H, Ramalho, RAG & Ribeiro, ARLP (1988) Intrahepatic distribution of vitamin A in humans and rats. Int J Vitam Nutr Res 58, 276280.Google ScholarPubMed
21 Arroyave, G, Chichester, CO, Flores, H, et al. (1982) Biochemical Methodology for the Assessment of Vitamin A Status. Washington: International Vitamin A Consultative Group, The Nutrition Foundation pp. 92.Google Scholar
22 Hess, D, Keller, HE, Oberlin, B, et al. (1991) Simultaneous determination of retinol, tocopherols, carotenes and lycopene in plasma by means of high-performance liquid chromatography on reversed phase. Int J Vitam Nutr Res 61, 232238.Google ScholarPubMed
23 Christian, P, West, KP Jr, Khatry, SK, et al. (1998) Night blindness of pregnancy in rural Nepal – nutritional and health risks. Int J Epidemiol 27, 231237.CrossRefGoogle ScholarPubMed
24 Biswas, AB, Mitra, NK, Chakraborty, I, et al. (2000) Evaluation of vitamin A status during pregnancy. J Indian Med Assoc 98, 525529.Google ScholarPubMed
25 Flores, H, Azevedo, MNA, Campos, FACS, et al. (1991) Serum vitamin A distribution curve for children aged 2–6y known to have adequate vitamin A status: a reference population. Am J Clin Nutr 54, 701711.CrossRefGoogle Scholar
26 World Health Organization (1996) Indicators for Assessing Vitamin A Deficiency and Their Application in Monitoring and Evaluating Intervention Programs. Geneva: WHO.Google Scholar
27 Sauberlich, HE, Apud Oliveira, JED, Marchini, JS, et al. (1994) Levantamento bibliográfico de estudos bioquímico-nutricionais sobre micronutrientes realizados no Brasil (Literature review of biochemical studies on micronutrients made in Brazil). Cad Nutr Rev Soc Bras Alim Nutr (São Paulo), 8, 3167.Google Scholar
28 Robles-Sardin, AE, Astiazarán-Gracia, M, Dávalos-Navarro, R, et al. (1998) Efecto de la suplementación con una dosis masiva de vitamina A en niños de 6 a 36 meses de edad (Effect of massive vitamin A supplement in children from 6 to 36 months of age). Salud Publica Mex 40, 309315.CrossRefGoogle Scholar
29 Morriss-Kay, GM & Sokolova, N (1996) Embryonic development and pattern formation. FASEB J 10, 961968.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Placental retinol and total carotenoid averages according to maternal and newborn vitamin A nutritional state(Mean values and standard deviations)

Figure 1

Table 2 Comparison of placental retinol and total carotenoid averages after logn transformation according to maternal and newborn vitamin A nutritional state(Mean values and standard deviations are presented as logn transformation)

Figure 2

Table 3 Sensitivity and specificity results according to serum cut-off points for vitamin A deficiency adopting the placental cut-off point 0·80 μmol/l according to analysis of the receiver operating characteristic curve