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1.
Acta Trop ; 123(2): 72-7, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22503377

ABSTRACT

In regions of high Plasmodium falciparum malaria endemicity, certain erythrocyte polymorphisms confer resistance to severe disease. In this study, we evaluate the role of the sickle cell trait (HbS) and ABO blood groups in the clinical manifestations of childhood malaria in Southwest Nigeria. The subjects comprised 3100 children (53% males, median age 39 months), including 1400 children with uncomplicated malaria, 1000 children with asymptomatic malaria and 700 with severe malaria. Haemoglobin (Hb) types were determined using electrophoresis and serum agglutination techniques were used to determine ABO blood groups. Blood group O was the commonest ABO blood group (47.7%) in the study population, the others were A (22.5%), B (25.2%) and AB (4.6%). The frequencies of the HbAS and HbAC were 14.4% and 5.8%, respectively. In regression models adjusting for age, gender, parasite density and blood group, HbAS was associated with a reduced risk of severe malaria OR=0.46 (CI(95%): 0.273-0.773). Among severe malaria subjects, HbAS was associated with significantly lower parasite densities. The protective effect of blood group O was demonstrated with a decreased risk of severe malaria OR=0.743 (CI(95%): 0.566-0.976) after adjusting for age, gender and parasite density and Hb genotype. Blood group B was associated with increased risk of severe malaria OR=1.638 (CI(95%): 1.128-2.380) after adjusting for age, gender, packed cell volume, parasite density and Hb genotype. We have confirmed from this large study of Nigerian children the major protective effective of the sickle cell heterozygous state against both cerebral malaria and severe malarial anaemia. We also show that the B blood group is associated with an increased risk of severe malaria. In conclusion, the sickle cell haemoglobin type and ABO groups modulate the risk of severe malaria in Nigerian children.


Subject(s)
ABO Blood-Group System/genetics , Genetic Predisposition to Disease , Malaria, Falciparum/physiopathology , Malaria, Falciparum/parasitology , Severity of Illness Index , Sickle Cell Trait/genetics , Anemia/epidemiology , Anemia/genetics , Anemia/parasitology , Anemia/physiopathology , Child , Child, Preschool , Female , Gene Frequency , Humans , Infant , Malaria, Cerebral/epidemiology , Malaria, Cerebral/genetics , Malaria, Cerebral/parasitology , Malaria, Cerebral/physiopathology , Malaria, Falciparum/epidemiology , Malaria, Falciparum/genetics , Male , Nigeria/epidemiology , Plasmodium falciparum/pathogenicity
2.
Afr J Med Med Sci ; 38(1): 87-92, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19722434

ABSTRACT

Many new innovations and advances are introduced into life and the sciences at a pace faster than any single individual can keep up with but human beings adjust to these changes at a much slower pace. Development is at snail speed in many developing countries and supersonic in the developed world and yet these have to interrelate. The introduction of medical technology and advances into developing countries is sometimes done haphazardly and often without prior appropriate education and decision making process. This has the potential to create dilemmas among stakeholders and engender conflicts with culture, religion and societal norms. A good grounding in the study of bioethical principles and theories is relevant to addressing current and evolving issues with changing biotechnology and shifting landmarks in today's highly technical clinical medicine. The knowledge and utilization of these principles should limit the occurrence of many scandals in the form and magnitude already recorded in the history of biomedical research and practice. While the debate as to whether ethics can be taught will continue, bioethics education provides the requisite knowledge and skill that are applicable at the bedside and in biomedical research. Some evidence has shown that formal teaching of ethics impacts positively on physicians and medical students' attitudes in the care of patients. In this paper we propose that bioethics as a distinct course should be incorporated into medical curriculum in Africa. The integration of bioethics as a required subject in the medical curriculum would have a positive impact on all aspects of health care and research. Real or assumed obstacles are not justifiable reasons for further delay in implementing this initiative


Subject(s)
Bioethics , Curriculum , Education, Medical, Undergraduate , Students, Medical , Africa , Humans
3.
J Pak Med Assoc ; 58(9): 501-5, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18846800

ABSTRACT

OBJECTIVE: To evaluate the relationship between measles virus (MV) antibodies (abs) in sera and breast milk of nursing mothers, their contributions in seroconversion of children (0-9 months) post vaccination, prevalence of prevaccination measles abs in sera of children brought for measles vaccination and seroconversion rate in vaccinees from nursing and lactating mothers. Also to determine the potency of vaccines available in Nigeria in relation to seroconversion. METHODS: One hundred and twenty pre- and post-vaccination sera and breast milk samples were collected from each nursing mother while corresponding number of finger prick pre- and post-vaccination sera samples were collected from children on filter papers. These were tested for mv abs using serological techniques. RESULTS: Eighty (20.0%) mothers had measles haemagglutination inhibition (HI) abs in sera and 88 (27.2%) had mv HI abs in breast milk. Eight (2.0%) children who had prevaccination mv abs in sera came from mv ab negative mothers. Forty-four (37.0%) came back for post vaccination sera, sero-converted while 76 (63.3%) gave low sero-conversion rate of 37.0%. Results showed that mv abs in sera or breast milk of mothers did not interfere with mv vaccination in children. The low sero-conversion rate obtained was due to low vaccine potency with titres ranging between (log10-10 - log10-2.5)TCID/per dose, besides non-specific antiviral substances exhibited virus neutralizing activity. CONCLUSION: Poor sero-conversion due to loss of passive immunity arose from undernourishment while low ab titres came with natural infection. This suggested mv vaccination did not immunize following natural mv infection or any other previous immune status.


Subject(s)
Measles Vaccine , Measles/blood , Age Factors , Child , Female , Health Surveys , Humans , Male , Measles/epidemiology , Measles/immunology , Measles/prevention & control , Milk, Human , Pakistan/epidemiology , Prevalence , Risk Factors , Seroepidemiologic Studies , Surveys and Questionnaires
4.
Ann Trop Med Parasitol ; 102(2): 95-102, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18318931

ABSTRACT

As the genetic diversity of Plasmodium falciparum infections in humans is implicated in the pathogenesis of malaria, the association between P. falciparum diversity at the merozoite surface protein-2 (msp2) locus and the severity of childhood malaria was investigated in Ibadan, in south-western Nigeria. The 400 children enrolled had acute uncomplicated malaria (144), cerebral malaria (64), severe malarial anaemia (67) or asymptomatic infections with P. falciparum (125). Nested PCR was used to investigate the msp2 genotype(s) of the parasites infecting each child. In terms of the complexity of infection and frequency of polyinfection, the children with asymptomatic infection were significantly different from those with uncomplicated malaria or severe malaria. The median number of FC27 alleles detected was higher in the asymptomatic children than in the symptomatic. After controlling for age and level of parasitaemia (with 'asymptomatic infection' as the reference category), a child in whom no FC27 alleles were detected was found to be at five-fold greater risk of uncomplicated malaria, and a child without polyinfection was found to have a three-fold increased risk of severe malarial anaemia and a six-fold increased risk of cerebral malaria. It therefore appears that msp2 genotypes are associated with asymptomatic carriage and that children with mono-infections are more likely to develop severe malaria than children with polyinfection.


Subject(s)
Antigens, Protozoan/genetics , Endemic Diseases , Malaria, Falciparum/genetics , Plasmodium falciparum/genetics , Alleles , Anemia/blood , Anemia/parasitology , Animals , Child, Preschool , Female , Genetic Variation , Genotype , Humans , Infant , Malaria, Cerebral/blood , Malaria, Cerebral/parasitology , Malaria, Falciparum/blood , Male , Merozoite Surface Protein 1/genetics , Nigeria , Protozoan Proteins/genetics , Severity of Illness Index
5.
Ann Trop Paediatr ; 25(4): 303-6, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16297306

ABSTRACT

Calcium and phosphate levels were investigated in 39 children with malaria (six severe and 33 uncomplicated) and in 39 healthy children. Hypocalcaemia (calcium <2.13 mmol/L, adjusted for albumin level) was detected in 23.1% of malaria cases and in 5.1% of controls, and hypophosphataemia (<1 mmol/L) in 38.5% of cases and in 15.4% of controls. Mean (SD) calcium levels in cases [2.26 (0/15)] were similar to those in controls [2.24 (0.12)]. In Nigerian children, hypocalcaemia and hypophosphataemia are associated with malaria.


Subject(s)
Calcium/blood , Malaria, Falciparum/blood , Phosphates/blood , Alkaline Phosphatase/blood , Child , Child, Preschool , Female , Hematocrit , Humans , Hypocalcemia/epidemiology , Hypophosphatemia/epidemiology , Infant , Malaria, Falciparum/parasitology , Male , Nigeria , Parasite Egg Count/methods , Serum Albumin/analysis
6.
Acta Trop ; 95(3): 226-32, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16023985

ABSTRACT

Genetic characteristics of Plasmodium falciparum may play a role in the clinical severity of malaria infection. We have studied the association between diversity at the merozoite surface protein-1 (msp-1) locus and the severity of disease in childhood malaria in Ibadan, south-west Nigeria. Two hundred and twenty-three children (median age of 34.5 months) presenting with malaria were enrolled into the study. They comprised 53 children with asymptomatic malaria (ASM), 101 with acute uncomplicated malaria (UM) and 69 with severe malaria (SM). Genotyping of the msp-1 locus was by polymerase chain reaction. The distribution of msp-1 alleles was significantly different between the three groups. Asymptomatic malaria samples had a higher median number of alleles than the other two groups. The type of msp-1 allele detected was significantly associated with the clinical category of malaria. The absence of K1 alleles was associated with a three-fold increase risk of UM and a four-fold increased risk of SM when compared with asymptomatic malaria. The absence of MAD20 alleles was associated with a five-fold increase risk of UM and an eight-fold increase of SM. We have found an association between the msp-1 locus of P. falciparum and clinical severity of malaria in a sample of Nigerian children. Our findings show that the presence of the K1 and MAD20 alleles was significantly associated with ASM and consequently a reduced risk of developing the symptomatic disease.


Subject(s)
Genetic Variation , Malaria, Falciparum/classification , Merozoite Surface Protein 1/genetics , Plasmodium falciparum/genetics , Animals , Child, Preschool , Female , Genotype , Humans , Malaria, Falciparum/genetics , Malaria, Falciparum/parasitology , Male , Nigeria , Severity of Illness Index
7.
Acta Trop ; 95(3): 248-55, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16002039

ABSTRACT

Plasmodium falciparum malaria remains a major public health hazard in sub-Saharan African children. While the factors that determine the variations in clinical outcome of a malaria have not been completely defined, both host and parasite factors, as well as the complex molecular interactions between them have been implicated. The cyto-adherent properties of the P. falciparum-infected red blood cells are considered as key properties in the pathogenesis of malaria and the polymorphisms of the host adhesion molecules could contribute to the severity of malaria. Clinical information and blood samples were collected from 223 children from Ibadan (south-west Nigeria), median age of 34.5 months, presenting with different clinical manifestations of malaria--clinically asymptomatic parasitism (ACP), acute uncomplicated malaria (UM) and severe malaria (SM)--as defined by WHO criteria. The polymorphisms of genes coding for four human adhesion molecules at six different loci (ICAM-1 exons 2, 4 and 6, E-selectin exon 2, CD36 exon 10, and PECAM exon 3) were studied. DNA samples were prepared for further genotyping of the six exons mentioned above by PCR-RFLPs using the appropriate restriction digests for each loci. The ICAM-1 exon 4 locus was monomorphic. All the other loci were at Hardy-Weinberg equilibrium (HWE). The E-selectin locus had very low heterozygosity (approximately 0.06) in contrast to the other loci under study (0.23-0.44). Once the data was further processed for covariates (age and parasite density) and taking as the reference category the ACP group, results show that in the presence of the G allele at the ICAM-1 exon 6 there is an increased risk (3.6 times) of severe malaria. As far as the T allele in the E-selectin exon is concerned, the number of sampled DNAs with the T allele within both the UM and SM categories is too low for drawing any relevant conclusion at this stage. In conclusion, these results suggest that genetic polymorphisms at host adhesion molecules loci are an important variable in the susceptibility to severe malaria. Further studies of host loci are needed to further delineate which polymorphisms are associated with severe malaria and increase our knowledge of the biology of host-parasite interactions.


Subject(s)
E-Selectin/genetics , Intercellular Adhesion Molecule-1/genetics , Malaria, Falciparum/genetics , Child, Preschool , Female , Humans , Malaria, Falciparum/blood , Malaria, Falciparum/classification , Male , Nigeria , Polymorphism, Genetic , Severity of Illness Index
8.
Phytother Res ; 17(10): 1173-6, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14669251

ABSTRACT

The anti-sickling activities of the extracts of the roots of a plant Cissus populnea L. (CPK) (a major constituent of a herbal formula Ajawaron HF used in the management of sickle cell disease in south-west Nigeria) has been examined. Phytochemical examination of the extract showed the presence of anthraquinone derivatives, steroidal glycosides and cardiac glycosides. Alkaloids and tannins were completely absent in the CPK extracts. Evaluation of the anti-sickling activity involved the use of both positive (p-hydroxybenzoic acid, 5 microg/mL) and negative control (normal saline) for each set of experiments aimed at the inhibition of sodium metabisulphite-induced sickling of the HbSS red blood cells obtained from confirmed non-crisis state sickle-cell patients. The chloroform and water partitioned fractions of the cold methanol extracts of CPK exhibited a 62.2% and 52.9% inhibition of sickling, respectively, at 180 min. The herbal formula (HF) aqueous extract showed the highest anti-sickling activity on a weight by weight basis of all the extracts and fractions tested, giving a 71.4% inhibition of sickling at the end of 180 min incubation when compared with the normal saline control. The maximum percentage inhibition of sickling exhibited by the p-hydroxybenzoic acid control was 46.0% at 90 min incubation.


Subject(s)
Antisickling Agents/pharmacology , Cissus , Erythrocytes, Abnormal/drug effects , Phytotherapy , Plant Extracts/pharmacology , Anemia, Sickle Cell/prevention & control , Antisickling Agents/administration & dosage , Antisickling Agents/therapeutic use , Humans , Medicine, African Traditional , Nigeria , Plant Extracts/administration & dosage , Plant Extracts/therapeutic use , Plant Roots , Sulfites
9.
J Trop Pediatr ; 49(1): 42-7, 2003 02.
Article in English | MEDLINE | ID: mdl-12630720

ABSTRACT

This study was carried out to determine the vitamin A status and nutritional intake of carotenoids of 213 children between the ages of 6 months and 6 years in a rural community in Nigeria. There were 109 males and 104 females. A total of 57 (26.8 per cent) children were deficient in serum retinol levels (< 10 microg/dl) while 102 (47.9 per cent) had low levels (10-19 microg/dl). The highest prevalence of serum retinol deficiency was in the 6-12 months age group, most of whom were breastfeeding and there was poor correlation between duration of breastfeeding and serum retinol levels. The prevalence of night-blindness was 1.5 per cent; however, none of the children had xerophthalmia. Chronically malnourished children had lower mean serum retinol levels than well nourished children. There was a high consumption of carotenoid-containing food, but despite this there was a high prevalence of vitamin A deficiency. We therefore suggest that measures to combat vitamin A deficiency should include vitamin A supplementation on a short-term basis. On a long-term basis parents should be educated on the importance of the consumption of locally available sources of provitamin A and pre-formed vitamin A rich foods, and the avoidance of overcooking. Parents should also be encouraged to grow more beta-carotene containing foods.


Subject(s)
Carotenoids/administration & dosage , Nutritional Status , Vitamin A/blood , Anthropometry , Child , Child, Preschool , Cross-Sectional Studies , Diet , Female , Humans , Infant , Male , Nigeria/epidemiology , Prevalence , Rural Population , Vitamin A Deficiency/blood , Vitamin A Deficiency/epidemiology
10.
West Afr J Med ; 21(1): 43-7, 2002.
Article in English | MEDLINE | ID: mdl-12081342

ABSTRACT

In view of the growing importance of the human immunodeficiency virus (HIV) infection and the Acquired Immunodeficiency Syndrome (AIDS) in Nigeria, 221 mothers were interviewed by means of semi-structured questionnaires in an infant welfare clinic in Ibadan, Nigeria, about their perceptions and beliefs about HIV/AIDS infection with particular emphasis on how the infection could be acquired, how the risk of its acquisition can be reduced and whether how children could be infected. The findings revealed that 81% of the respondents believe that HIV infection does exist in Nigeria but only 17.6% think they have seen an AIDS patient. About two-thirds (68.8%) believe that children can be infected with HIV, 70.6% believe that a mother can transmit the infection to her child and 58% believe that HIV can be transmitted through breast milk. Eighty percent believe that people can protect themselves from having the infection by various means, including avoiding sharing needles or reusing hypodermic needles (83.3%), receiving unscreened blood (79.2%), mutual fidelity with a single sexual partner (73.8%), use of condoms (67.9%), avoiding the use of public toilets (56.1%) and avoiding mosquito bites (35.3%). Those with higher education showed better knowledge than those with lower education. In spite of the strong correlation with formal education, some misconceptions existed in all groups. For example, those without any formal education compared with those with some formal education believed that use of public toilet can cause HIV to be transmitted, the difference was not statistically significant (chi2 = 8.87; p = 0.064). Interestingly more of the highly literate women believed that HIV infection can be acquired by mosquito bites (chi2 = 16.82; p = 0.002). It was concluded that awareness of HIV infection and AIDS is high among mothers of infants attending the infant welfare clinic of the Institute of child Health, Ibadan. Whatever educational interventions is planned for this facility should take these findings into account and specially target those with none or little formal education.


Subject(s)
HIV Infections/psychology , Health Knowledge, Attitudes, Practice , Mothers , Acquired Immunodeficiency Syndrome/etiology , Acquired Immunodeficiency Syndrome/psychology , Adult , Chi-Square Distribution , Child , Female , HIV Infections/etiology , Humans , Middle Aged , Mothers/education , Nigeria , Risk Factors
11.
Ethn Dis ; 12(2): 207-12, 2002.
Article in English | MEDLINE | ID: mdl-12019929

ABSTRACT

High sodium intake is associated with high levels of blood pressure, both among and within populations. However, there have been few intervention studies from Africa reporting blood pressure changes with dietary reduction of sodium. In this study, we tested the feasibility of achieving a reduction in dietary sodium intake in free-living individuals using a dietary intervention among 82 free-living normotensive adults in southwest Nigeria. The participants, 49 men (mean age 47.2 years) and 33 women (mean age 43.6 years), received dietary advice to reduce sodium intake and maintained the reduced sodium diet for a 2-week period. Blood pressure and 24-hour urinary excretion of sodium were measured at baseline and after two weeks on the reduced sodium diet. Baseline 24-hour urinary sodium excretion was 140.5 (SD 53.4) mmol/24 hours among men and 132.6 (SD 48.0) mmol/24 hours among women. Twenty-four hour urinary sodium excretion fell by 76.9 (95% Cl 59.7, 94.1) mmol/24 hours among men, and by 79.4 (95% Cl 59.4, 99.1) mmol/24 hours among women. On the low sodium diet, systolic blood pressure fell by 4.7 (95% CI 1.9, 7.4) mm Hg among men, and by 7.0 (95% CI 2.6, 11.4) mm Hg among women while diastolic blood pressure fell by 1.9 (95% CI -0.3, 4.1) mm Hg among men and by 1.6 (95% CI -1.8, 5.0) mm Hg among women. It is concluded that a significant reduction in sodium intake may be achievable in free-living individuals in this setting using a simple dietary intervention. The findings of this pilot study should encourage more sophisticated intervention studies (such as cross-over trials and double blind randomized clinical trials) in Africans for the elucidation of mechanisms and consequences of hypertension in Blacks.


Subject(s)
Health Behavior , Health Education , Sodium, Dietary/administration & dosage , Adult , Blood Pressure , Feasibility Studies , Female , Humans , Hypertension/prevention & control , Male , Middle Aged , Nigeria , Pilot Projects , Sodium/urine
12.
J Health Popul Nutr ; 18(3): 139-44, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11262766

ABSTRACT

A community survey of treatment regimens for acute diarrhoea in children was carried out in 10 villages in the Ona Ara Local Government Area of Oyo State, Nigeria, using a combination of qualitative (focus-group discussions) and quantitative (weekly surveillance of diarrhoea) methods. Focus-group discussions were conducted with parents of children aged less than 5 years, while a surveillance of diarrhoea among 550 children of same age was carried out during a 6-month period. The findings of the study showed that not all types of diarrhoea were recognized as illnesses, and only those considered to be illnesses were treated. Treatment often involved an adhoc group which comprised adults who were present at the time the illness occurred (including parents, neighbours, relatives, and elders). Certain beliefs and practices, such as associating types of diarrhoea with occupation or ethnic groups, categorizing the severity on perceived causes, and withholding certain foods during episodes of diarrhoea, were common factors in decision-making for seeking treatment. Antimicrobial agents were used in the case of 46.8% of 205 diarrhoeal episodes, and 28.5% were not at all treated. The usual practice of focusing on a target group, such as mothers, during educational interventions may need to be modified in communities where nearly every adult has a role in decision-making in relation to health. The need to adapt health policy and programmes to cultural norms should be addressed to improve the impact of programmes.


Subject(s)
Cultural Characteristics , Diarrhea, Infantile/therapy , Diarrhea/therapy , Health Policy , Child, Preschool , Female , Focus Groups , Health Knowledge, Attitudes, Practice , Humans , Infant , Male , Nigeria , Population Surveillance
13.
Afr J Med Med Sci ; 29(2): 145-9, 2000 Jun.
Article in English | MEDLINE | ID: mdl-11379447

ABSTRACT

The effectiveness of rice flour and maize flour based oral rehydration solution (ORS) in treating mild and moderate dehydration was studied among 88 children aged to 6 to 42 months at the Oni Memorial Children Hospital, Ibadan. In this randomized clinical trial, fifty children were treated with rice-based ORS while fifty-three received the maize-based ORS, over a four hour period. There was clinical improvement in the signs of dehydration with a significant increase in body weights and a significant fall in the packed cell volume following the administration of the two preparations. The maize-ORS contains 4.3 g protein, 179.3 Kilocalories and rice-ORS contains 3.6 g protein and 152.1 Kilocalories per litre of the preparation, respectively. It is concluded that rice and maize based ORS were acceptable and effective in oral rehydration of diarrhoea patients. They may also contribute to the nutrient intake of patients with (mild to moderate) 'some' dehydration. However other sources of energy, protein and mineral intake should be continued in these patients.


Subject(s)
Dehydration/therapy , Flour/analysis , Fluid Therapy/methods , Oryza/chemistry , Rehydration Solutions/analysis , Rehydration Solutions/chemistry , Zea mays/chemistry , Body Weight , Child, Preschool , Dehydration/blood , Dehydration/classification , Dehydration/diagnosis , Dietary Carbohydrates/administration & dosage , Dietary Carbohydrates/analysis , Dietary Fats/administration & dosage , Dietary Fats/analysis , Dietary Fiber/administration & dosage , Dietary Fiber/analysis , Dietary Proteins/administration & dosage , Dietary Proteins/analysis , Energy Intake , Erythrocyte Indices , Female , Humans , Infant , Male , Nigeria , Nutrition Assessment , Nutritional Requirements , Nutritional Status , Nutritive Value , Severity of Illness Index
14.
Early Hum Dev ; 54(3): 207-14, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10321787

ABSTRACT

There is scanty data in the literature on the variation of fontanelle size with gestational age. This relationship was studied in 250 neonates delivered at gestational ages of 29-41 weeks at the University College Hospital, Ibadan, Nigeria. Anterior fontanelle size showed a low positive correlation with gestational age (r = 0.15). However, controlling for occipitofrontal circumference reduced this correlation to 0.12. Mean anterior fontanelle size increased with increasing gestational age but the anterior fontanelle size: occipitofrontal circumference ratio remained remarkably constant over the range of gestational age studied. The posterior fontanelle size did not show a significant correlation with gestational age and the prevalence of closed posterior fontanelles at birth did not differ significantly between term and preterm neonates. It is concluded that anterior fontanelle size does show a low positive correlation with gestational age but maintains the same ratio with head circumference at least during the third trimester of intrauterine life. Posterior fontanelle size shows no linear relationship with gestational age.


Subject(s)
Gestational Age , Skull/anatomy & histology , Female , Humans , Infant, Newborn , Male , Reference Values
15.
J Trop Pediatr ; 45(2): 66-70, 1999 04.
Article in English | MEDLINE | ID: mdl-10341498

ABSTRACT

A community-based survey to determine the prevalence of human T-cell lymphotropic type I (HTLV-I) and type II (HTLV-II) virus infections in mothers and children in south-western Nigeria was carried out using blood samples collected in 1993. A multistage cluster, random sampling procedure was used to select 460 mother-child pairs (476 children because there were 16 sets of twins) from 14 enumeration areas. A commercially available, whole HTLV-I lysate antigen-based ELISA method was used to screen for HTLV-I and HTLV-II antibodies in the samples. A synthetic peptide antigen-based ELISA was then used to differentiate between antibody reactivity to either HTLV-I or HTLV-II. Reactivity to HTLV-I or HTLV-II antibodies was found in 4.3 per cent (20/460) of mothers and in 1.1 per cent (5/476) of children in both rural and urban communities and all the positive children were males. None of the 16 sets of twins in this study was positive for either HTLV-I or HTLV-II. Also none of the mother-child paired sera tested showed concordance for either HTLV-I or HTLV-II antibody positivity. The lack of concordance between mother and child sera suggests that vertical transmission may not be the major route of transmission of HTLV infection to children in south-western Nigeria. Other modes of transmission, such as the re-use of unsterilized needles for injections and surgical knives in local scarification, which are common practices in the region, need to be investigated as they may prove to be more important than vertical transmission. These findings have important implications for any control programme for diseases that can be spread by the same routes as HTLV infection (the human immunodeficiency viruses, hepatitis B, and hepatitis C infections).


Subject(s)
HTLV-I Infections/epidemiology , HTLV-II Infections/epidemiology , Adult , Child , Child, Preschool , Female , HTLV-I Infections/transmission , HTLV-II Infections/transmission , Humans , Infant , Infectious Disease Transmission, Vertical/statistics & numerical data , Nigeria/epidemiology , Seroepidemiologic Studies
16.
West Afr J Med ; 18(1): 55-9, 1999.
Article in English | MEDLINE | ID: mdl-10876734

ABSTRACT

Fontanelle sizes were studied in 200 term and appropriate-for-gestational age neonates delivered at the University College Hospital, Ibadan, Nigeria with the aim of determining their normal range of variation. The anterior and posterior fontanelle sizes were described using the range, mean, standard deviation and selected (3rd, 25th, 50th, 75th and 97th) percentiles. The anterior fontanelle size ranged from 1.0 to 6.4 cm with a mean of 4.0 (SD 1.0) cm. The posterior fontanelle size ranged from 0.0 to 5.5 cm with a mean of 1.4 (SD 1.7) cm. The posterior fontanelle was not palpable in 99 (49.5%) of the neonates and there was no association between the sex of the neonate and posterior fontanelle closure (X2 = 0.97, p = 0.325). The findings of the study are consistent with those of other workers who have documented larger anterior fontanelle sizes in the Negro neonate compared to his caucasian counterpart. However, the anterior fontanelle size in this study was larger than previously reported Nigerian figures, a fact which may be due to the exclusion of neonates who still had overriding cranial bones (from excessive moulding) at the time the measurements were taken. It is suggested that local values derived from well-defined populations be used as reference in the evaluation of the child with dysmorphic features in order to avoid errors of classification due to racial differences in the normal range of variation. Further studies of this nature are needed in order to delineate such differences where they exist.


Subject(s)
Infant, Newborn , Skull/anatomy & histology , Birth Weight , Black People , Female , Gestational Age , Humans , Male , Nigeria , Reference Values , White People
18.
West Afr J Med ; 18(4): 294-7, 1999.
Article in English | MEDLINE | ID: mdl-10734795

ABSTRACT

The ABO and Rhesus blood group systems remain the most important blood group systems clinically. In order to provide gene frequency values for the ABO and Rh (D) alleles in a healthy infant population in south west Nigeria, 4748 healthy infants were typed for ABO and Rh (D) blood groups over a five year period (1988-1992). Overall, 2575 (54.2%) were blood group O, 1023 (21.6%) were blood group A, 1017 (21.4%) were blood group B and 133 (2.8%) were blood group AB. The distribution of the ABO blood groups did not differ significantly from those expected under the Hardy Weinberg equilibrium (Goodness-of-fit X2 = 6.09, df = 3, p = 0.1075). The proportions of the infants belonging to the various ABO blood groups did not vary significantly over the period of the study (X2 = 14.53, df = 12, p = 0.268). Overall gene frequencies for the O, A and B genes were 0.7398, 0.1305 and 0.1298 respectively. For the Rh (D) gene, 4520 (95.2%) were Rh-positive while 228 (4.8%) were Rh-negative. However, the proportions of Rh (D) negative infants varied significantly over the period of the study, with a particular year (1991) having nearly twice the usual frequency of Rh-negative individuals (X2 = 31.17, df =, p < 0.001). The frequency of the Rh (D) gene was 0.7809. These figures are reported in the hope that they may find some use as reference for studies of ABO blood groups in health and disease, especially since they were obtained in an infant population in which it is expected that selection pressures should not have started to act to any significant extent.


Subject(s)
ABO Blood-Group System/genetics , Gene Frequency/genetics , Infant, Newborn/blood , Rh-Hr Blood-Group System/genetics , Alleles , Blood Grouping and Crossmatching , Genetics, Population , Genotype , Humans , Nigeria , Phenotype , Reference Values , Urban Population/statistics & numerical data
19.
East Afr Med J ; 75(5): 304-7, 1998 May.
Article in English | MEDLINE | ID: mdl-9747004

ABSTRACT

A study of selected facial and ear dimensions in 200 term and appropriate-for-gestational age neonates delivered at the University College Hospital, Ibadan, Nigeria, was carried out with the aim of describing their normal range of variation and providing reference values for clinical use. The features studied included inner canthal distance, outer canthal distance, palpebral fissure length, nasolabial distance, oral intercommissural length, total ear length and ear length above the eyeline. The inner canthal distance ranged from 1.6 to 2.5 cm with a mean of 2.1 (SD 0.2) cm while the outer canthal distance ranged from 5.2 to 7.2 cm with a mean of 6.1 (SD 0.4) cm. The oral intercommissural length ranged from 2.5 to 4.0 cm with a mean of 3.1 (0.3) cm and the total ear length ranged from 2.4 to 4.0 cm with a mean of 3.2 (SD 0.3) cm. Three per cent of the neonates had the whole ear located completely below the eye line. No significant sex differences in the mean values of any of the dimensions studied were found. The findings of the study are consistent with those of other workers who have documented shorter ears in the Negro neonate compared to his Caucasian counterpart. It is suggested that local values derived from well-defined populations be used as reference in the evaluation of the child with dysmorphic features in order to avoid errors of classification due to racial variations in the range of normal.


Subject(s)
Black People , Ear/anatomy & histology , Face/anatomy & histology , Infant, Newborn , Anthropometry , Female , Humans , Male , Nigeria , Reference Values , White People
20.
West Afr J Med ; 17(2): 91-4, 1998.
Article in English | MEDLINE | ID: mdl-9715113

ABSTRACT

The experience of a Nigerian infant welfare clinic in offering sickle cell haemoglo-binopathy (SCH) screening by electrophoresis to its clinic population over a 12-year period is reported. Overall 10,115 children were screened. Homozygous haemoglobin S was detected in 3.1% and haemoglobin S + C in 1.1%. Carriers of the sickle cell gene (haemoglobin A + S) comprised 23.7% of the children screened. Gene frequencies for the A, S and C genes were 0.814, 0.155 and 0.031 respectively. The gene frequencies of the S and C genes were higher than those reported in infants and under-five children from other parts of Nigeria. Screening for sickle cell haemoglobinopathy in the first year of life through infant welfare clinics and 'well-baby' clinics as described in this report is suggested as a viable approach to the problems of detection (and genetic counselling) of SCH in developing countries with their scant resources. The advantages and limitations of this approach are discussed.


Subject(s)
Blood Protein Electrophoresis , Developing Countries , Hemoglobin SC Disease/prevention & control , Sickle Cell Trait/prevention & control , Female , Genetic Carrier Screening , Hemoglobin SC Disease/genetics , Humans , Infant , Infant Welfare , Male , Nigeria , Sickle Cell Trait/genetics
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