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Volume 2012 (2012), Article ID 789706, 4 pages
Decreased Vitamin B12 Levels in Children with Nocturnal Enuresis
1Department of Urology, Faculty of Medicine, Kahramanmaras Sutcu Imam University, Yörükselim Mahallesi Hastane Caddesi 32, 46100 Kahramanmaras, Turkey
2Department of Pediatrics, Faculty of Medicine, Kahramanmaras Sutcu Imam University, 46100 Kahramanmaras, Turkey
3Department of Pediatric Surgery, Faculty of Medicine, Kahramanmaras Sutcu Imam University, 46100 Kahramanmaras, Turkey
Received 11 November 2011; Accepted 5 December 2011
Academic Editors: U. Barroso and H. Tezval
Copyright © 2012 Bülent Altunoluk et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Objectives. Nocturnal enuresis is a common pediatric problem, the etiology of which is unclear. In the present study, vitamin B12 and folate levels were measured in children with nocturnal enuresis and compared with those in healthy control group children to investigate whether there was any relation with enuresis and neurogenic maturation as a first time in the literature. Methods. In this cross-sectional study, we included thirty children (16 girls, 14 boys) who had presented with primary nocturnal enuresis (PNE) complaints in the study group and 31 children (13 girls, 18 boys) in the control group. Body weight and height measurements were obtained and complete blood counts and vitamin B12 and folate levels were measured in all children. Results. No difference was found in age, height, and weight between study and control groups. Also the mean levels of the hemoglobin, hematocrit, and mean corpuscular volume (MCV) were not different between the two groups. Significantly lower mean vitamin B12 and folate levels were found in the enuresis group compared with the control group. Conclusions. Further studies are needed to clarify B12 and folate deficiency in larger series so that these tests can be included in routine investigations of enuretic children.
Primary nocturnal enuresis (PNE) is defined as involuntary voiding during the night in children after the age at which bladder control would normally be expected and is the most common voiding problem in pediatric population . Because of its high prevalence, nocturnal enuresis has remained a focus of extensive scientific research over the past few decades. The etiology of PNE has been widely debated but is still not completely understood. The most commonly established causes of nocturnal enuresis are small bladder size, abnormal sleep patterns, the high amount of urine produced during sleep at night, and delayed functional maturation of the central nervous system [2, 3].
Vitamin B12 and folate play an important role in the metabolism, development, and maturation of the nervous system, even though their exact roles in the normal and pathologic conditions are not fully understood. In spite of extensive researches on PNE, many questions still remain unanswered regarding its exact pathophysiology. According to the best of our knowledge, there is no study that investigated serum vitamin B12 and folate levels in children with PNE in the English literature.
In the present study, vitamin B12 and folate levels were measured in children with nocturnal enuresis and compared with those in healthy control group children to investigate whether there was any relation with enuresis and neurogenic maturation as a first time in the literature.
2. Material and Methods
In this study, the study group comprised of prospectively recruited 30 children with nocturnal enuresis. Primer nocturnal enuresis was defined as bed-wetting in a child who never had a dry period for over 6 months according to the International Children Continence Society recommendations . Enuretic children were selected among new consecutive referrals to our outpatient clinics meeting the following inclusion criteria: a frequency of two or more enuretic episodes per week, no associated daytime wetting, no dry period of more than 3-month duration since birth, normal pubertal stage for age assessed by the Tanner staging , no neurological or urological abnormalities, normal blood biochemical analysis, normal urine analysis, including urinary culture, no history of previous urinary tract infection, and no other signs or symptoms of any chronic illness. Thirty-one matched healthy children with similar age and without enuresis were included as the control group. Children having a current or prior history of nervous system diseases were not included.
Body weight and height measurements of the children were obtained carefully by the same experienced personnel. Complete blood counts and vitamin B12 and folate levels were measured in all children. The cutoff points used for serum folic acid were <3 ng/ml for deficiency, 3–6 ng/mL for low levels, and >6 ng/mL for normal values. Vitamin B12 deficiency was defined as serum concentration below 200 pg/mL, normal range 200 to 900 pg/mL, and excess >900 pg/mL.
Institutional Local Ethics Committee approved the study protocol, and written informed consent was obtained from the parents of the children after explaining the nature of the procedures. The results were expressed as mean ± standard deviation (SD) and the range. The paired samples -test and Mann-Whitney test were used for statistical analyses. A value less than 0.05 was considered statistically significant.
Thirty children (16 girls, 14 boys) in the study group and 31 children (13 girls, 18 boys) in the control group were enrolled in the study. The mean age of the children in the enuresis group was 9.3 ± 2.7 years (range 5–14 years) and 9.52 ± 1.9 years (range 5–14 years) in the control group. Of 61 subjects included in the study, no difference was found in age, height, and weight between study and control groups (; Table 1). In addition, the mean levels of the hemoglobin, hematocrit, and mean corpuscular volume (MCV) were not different between the two groups (; Table 1). The parental history of enuresis was seen in 22 of 30 children in the enuresis group. On the other hand, in the control group there was no parental history of nocturnal enuresis (Table 1). Significantly lower mean vitamin B12 and folate levels were found in the enuresis group compared with the control group ( and , resp. Table 2). Also, the number of children with vitamin B12 deficiency in the enuretic group was significantly higher than that in the control group ( (30%) versus (0%), ). With regard to folate deficiency, there was no folate deficiency in the control group, while there were two (6.7%) children with low serum folic acid levels in the enuretic group (Table 2).
In the present study children with primary nocturnal enuresis tended to have lower vitamin B12 and folate levels than those of the control children. We searched medical indexes about serum vitamin B12 and folate levels in enuresis and found no study dealing with this topic. Therefore this is the first study that investigated B12 and folate levels in enuretic children.
Nocturnal enuresis is the repeated, involuntary loss of urine during sleep . Bed-wetting spontaneously ceases with increasing age, being present in 15% of 5-year-old children, 5% of 10-year-old children, and 1% of 15-year-old children. Despite extensive research, there is still significant controversy regarding its etiology, and it is now generally accepted that multiple pathologic factors are probably involved.
Theories reported as the probable causes of enuresis delayed central nervous system maturation, psychogenic and behavioral components, environmental influences, deep sleep, allergies, small bladder capacity, uninhibited neurogenic bladder contractions, structural abnormalities of the urinary tract, lack of diurnal variation of vasopressin, nocturnal hypercalciuria, prostaglandin production, and sleep apnea [7–10].
Although nocturnal enuresis is one of the common problems among children, the pathophysiology of this disorder remains unclear. The most commonly emphasized pathophysiologic theory of nocturnal enuresis proposes a delayed functional maturation of the central nervous system control on the bladder at night. Factors that support this delayed maturation theory include a significant spontaneous cure rate with the increasing of age, the results of urodynamic assessments demonstrating a reduced functional bladder capacity, association of delayed motor development, a proposed deficiency in endocrine maturation, and the documented hereditary aspect of enuresis [2, 11, 12]. Additionally, retardation in the growth rate, decreased bone age and bone mineral density determined in children with nocturnal enuresis may reflect delayed maturation of regulatory central nervous system functions [3, 13].
Although there is as yet no direct neuroanatomical evidence for this hypothesis it is supported by the decrease in enuresis with advancing age so that fifteen percent of these children become dry at night each year, attesting to its developmental nature [6, 14].
Because of the unclear etiopathogenesis, we measured the levels of vitamin B12 and folate, effective on the neurogenic maturation, in enuretic children. Vitamin B12 and folate levels were found significantly lower in the enuresis group compared with the control group. Neurologic disease due to a lack of vitamin B12 is a clinical entity. Deficiency of vitamin B12 affects particularly hematopoietic, epithelial, and nervous tissues but the exact role of vitamin B12 in the metabolism of the nervous system remains unclear . Deficiency of vitamin B12 affects mainly the central nervous system and tissues with fast mitotic activity, such as hematopoietic and digestive tract epithelium [16, 17]. The main systems affected due to B12 deficiency are the hematological, skin, and mucous membranes and the nervous system. Neurological features are attributable to pathology in the peripheral nerves, optic nerves, and posterior and lateral columns of the spinal cord and brain. B12 deficiency causes a wide spectrum of neurological manifestations ranging from neural tube defects to changes in cognition and behavior [18–20].
It is not known how cobalamin deficiency causes neurologic problems. During a deficiency state of B12, methylmalonyl-CoA accumulates and is used instead of acetyl-CoA in the synthesis of fatty acids. This results in unstable myelin that degrades more easily and has damaging effects on neurological development of growing children .
Folates are vitamins essential to the development of the central nervous system. Insufficient folate activity at the time of conception and early pregnancy can result in congenital neural tube defects. Folate is particularly important during the early development of the brain. Folate deficiency can cause megaloblastic anaemia, congestive heart failure, pigmentation, premature greying of hair, infertility, cervical dysplasia, uterine dysplasia, neuropathy, psychiatric disorders, cognitive dysfunction, and dementia. Behavioural abnormalities have been noted in folate-deficient mice .
The family history is one key because if one parent wets the bed, 44% of his or her children will do so and if both parents wet the bed, 77% of their children will do so .
PNE is believed by many investigators to be due to a maturational delay of the central nervous system connections necessary for nocturnal bladder control .
A limitation of our study is the small sample size. Further prospective studies with larger series are needed.
In conclusion, if B12 and folate deficiency will be detected in larger series, these tests can be included in routine investigations of enuretic children. Hence, in those children with low levels, the efficacy of the supplementation treatment may be investigated.
Conflict of Interests
The authors declare no conflict of interests.
- H. G. Rushton, “Wetting and functional voiding disorders,” Urologic Clinics of North America, vol. 22, no. 1, pp. 75–93, 1995.
- S. D. Mark and J. D. Frank, “Nocturnal enuresis,” British Journal of Urology, vol. 75, no. 4, pp. 427–434, 1995.
- B. Nuhoǧlu, A. Ayyildiz, V. Fidan, Ö. Cebeci, U. Koşar, and C. Germiyanoǧlu, “Do children with primary nocturnal enuresis have a retarded bone age? A cross-sectional study,” International Journal of Urology, vol. 13, no. 2, pp. 109–110, 2006.
- J. P. Noørgaard, J. D. van Gool, K. Hjälmås, J. C. Djurhuus, and A. L. Hellström, “Standardization and definitions in lower urinary tract dysfunction in children,” British Journal of Urology, vol. 81, no. 3, pp. 1–16, 1998.
- J. M. Tanner and R. H. Whitehouse, “Clinical longitudinal standards for height, weight, height velocity, weight velocity, and stages of puberty,” Archives of Disease in Childhood, vol. 51, no. 3, pp. 170–179, 1976.
- R. B. Nadler, W. Bushman, and A. W. Wyker, “Standart diagnostic considerations,” in Adult and Pediatric Urology, J. Y. Gillenwater, J. T. Grayhack, S. S. Howards, and M. E. Mitchell, Eds., vol. 1, pp. 47–64, Lippincott Williams & Wilkins, Philadelphia, Pa, USA, 2002.
- J. C. Djurhuus, J. P. Norgaard, K. Hjalmas, and S. Wille, “Nocturnal enuresis: a new strategy for treatment against a physiological background,” Scandinavian Journal of Urology and Nephrology, Supplement, no. 143, pp. 3–29, 1992.
- J. B. Lennert and J. J. Mowad, “Enuresis: evaluation of perplexing symptom,” Urology, vol. 13, no. 1, pp. 27–29, 1979.
- Y. V. Natochin and A. A. Kuznetsova, “Nocturnal enuresis: correction of renal function by desmopressin and diclofenac,” Pediatric Nephrology, vol. 14, no. 1, pp. 42–47, 2000.
- U. Çinar, C. Vural, B. Çakir, E. Topuz, M. I. Karaman, and S. Turgut, “Nocturnal enuresis and upper airway obstruction,” International Journal of Pediatric Otorhinolaryngology, vol. 59, no. 2, pp. 115–118, 2001.
- M. R. Järvelin, “Development history and neurological findings in enuretic children,” Developmental Medicine & Child Neurology, vol. 31, pp. 728–736, 1989.
- M. R. Dündaröz, S. Ü. Sarici, M. Denli, H. I. Aydin, M. Kocaoǧlu, and T. Özişik, “Bone age in children with nocturnal enuresis,” International Urology and Nephrology, vol. 32, no. 3, pp. 389–391, 2001.
- M. Mimouni, A. Shuper, and F. Mimouni, “Retarded skeletal maturation in children with primary enuresis,” European Journal of Pediatrics, vol. 144, no. 3, pp. 234–235, 1985.
- K. Hjälmås, “Pathophysiology and impact of nocturnal enuresis,” Acta Paediatrica, International Journal of Paediatrics, vol. 86, no. 9, pp. 919–922, 1997.
- K. O. Lövblad, G. Ramelli, L. Remonda, A. C. Nirkko, C. Ozdoba, and G. Schroth, “Retardation of myelination due to dietary vitamin deficiency: cranial MRI findings,” Pediatric Radiology, vol. 27, no. 2, pp. 155–158, 1997.
- S. M. Graham, O. M. Arvela, and G. A. Wise, “Long-term neurologic consequences of nutritional vitamin deficiency in infants,” Journal of Pediatrics, vol. 121, no. 5, pp. 710–714, 1992.
- E. B. Casella, M. Valente, J. M. de Navarro, and F. Kok, “Vitamin deficiency in infancy as a cause of developmental regression,” Brain and Development, vol. 27, no. 8, pp. 592–594, 2005.
- P. N. Kirke, A. M. Molloy, L. E. Daly, H. Burke, D. G. Weir, and J. M. Scott, “Maternal plasma folate and vitamin are independent risk factors for neural tube defects,” Quarterly Journal of Medicine, vol. 86, no. 11, pp. 703–708, 1993.
- S. D. Shorvon, M. W. P. Carney, I. Chanarin, and E. H. Reynolds, “The neuropsychiatry of megaloblastic anaemia,” British Medical Journal, vol. 281, no. 6247, pp. 1036–1038, 1980.
- S. Aaron, S. Kumar, J. Vijayan, J. Jacob, M. Alexander, and C. Gnanamuthu, “Clinical and laboratory features and response to treatment in patients presenting with vitamin deficiency-related neurological syndromes,” Neurology India, vol. 53, no. 1, pp. 55–58, 2005.
- L. H. Allen, J. L. Rosado, J. E. Casterline et al., “Vitamin B-12 deficiency and malabsorption are highly prevalent in rural Mexican communities,” American Journal of Clinical Nutrition, vol. 62, no. 5, pp. 1013–1019, 1995.
- S. M. Gospe, D. W. Gietzen, P. J. Summers et al., “Behavioral and neurochemical changes in folate-deficient mice,” Physiology and Behavior, vol. 58, no. 5, pp. 935–941, 1995.
- H. Bakwin, “The genetics of enuresis,” in Bladder Control and Enuresis, I. Kolvin, R. C. MacKeith, and S. R. Meadow, Eds., pp. 73–77, William Heinemann Medical Books Ltd, 1973.