Gender differences in best friendships

Prior investigations of friendship patterns have reported gender differences, with women's same-gender friendships tending to be richer and having a possible therapeutic value, as compared to those of men. Compared to same-gender best friendships, opposite-gender best friendships have been described as less fulfilling for women and more fulfilling for men. The present study explored such differences more fully in a sample of 65 female and 58 male predominantly white college students. Subjects completed four modified versions of P. H. Wright's [(1985) “The Acquaintance Description Form,” In S. F. Duck and D. Pearlman (Eds.), Understanding Personal Relationships: An Interdisciplinarian Approach, London: Sage] Acquaintance Description Form, describing their actual and ideal same-gender best friendships and their actual and ideal opposite-gender best friendships. They also responded to several measures of dysphoria. In the present study, the lowest scores for the friendship scales were reported by male subjects describing same-gender friendships, both ideal and actual. For both male and female subjects, dysphoria was positively correlated with a discrepancy between ideal and actual friendships with same-gender or opposite-gender individuals.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/45601/1/11199_2004_Article_BF00289323.pd

Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure.

Dihydropyrimidine dehydrogenase (DPD) deficiency is an autosomal recessive disease characterized by thymine-uraciluria in homozygous deficient patients. Cancer patients with a partial deficiency of DPD are at risk of developing severe life-threatening toxicities after the administration of 5-fluorouracil. Thus, identification of novel disease-causing mutations is of the utmost importance to allow screening of patients at risk. In eight patients presenting with a complete DPD deficiency, a considerable variation in the clinical presentation was noted. Whereas motor retardation was observed in all patients, no patients presented with convulsive disorders. In this group of patients, nine novel mutations were identified including one deletion of two nucleotides [1039-1042delTG] and eight missense mutations. Analysis of the crystal structure of pig DPD suggested that five out of eight amino acid exchanges present in these patients with a complete DPD deficiency, Pro86Leu, Ser201Arg, Ser492Leu, Asp949Val and His978Arg, interfered directly or indirectly with cofactor binding or electron transport. Furthermore, the mutations Ile560Ser and Tyr211Cys most likely affected the structural integrity of the DPD protein. Only the effect of the Ile370Val and a previously identified Cys29Arg mutation could not be readily explained by analysis of the three-dimensional structure of the DPD enzyme, suggesting that at least the latter might be a common polymorphism. Our data demonstrate for the first time the possible consequences of missense mutations in the DPD gene on the function and stability of the DPD enzyme

Anemia em escolares da primeira série do ensino fundamental da rede pública de Maceió, Alagoas, Brasil Anemia in public school first graders in the city of Maceió, Alagoas, Brazil

Realizou-se um estudo transversal com amostra probabilística de 426 alunos de 6 a 10 anos, da 1ª série do ensino fundamental das escolas públicas de Maceió, Alagoas, Brasil. O objetivo foi avaliar a prevalência da anemia e sua associação com o retardo de crescimento. Os dados foram coletados entre maio e julho de 2000. O sangue foi colhido por venipuntura e a dosagem de hemoglobina (Hb) foi realizada pelo contador Coulter STKS. Classificou-se a anemia por dois critérios estabelecidos pela Organização Mundial da Saúde: Hb <11,5g/dl e Hb <12,0g/dl. O retardo pondo-estatural foi diagnosticado quando os indicadores Altura/Idade (A/I), Peso/Idade (P/I) e Peso/Altura (P/A) se encontravam abaixo de -2,0 desvios-padrão da referência NCHS. A prevalência da anemia foi de 9,9%, considerando-se Hb <11,5g/dl e de 25,4%, utilizando-se Hb <12,0g/dl. O retardo do crescimento foi detectado em 6,2% segundo A/I, 4,0% pelo indicador P/I e 3,0% em relação a P/A. Não houve associação estatisticamente significativa entre as variáveis do estudo. Estes resultados confirmam os observados em outras pesquisas: prevalência de anemia muito superior à prevalência do retardo pondo-estatural. Conclui-se que as graves conseqüências da anemia nesta faixa etária, justificam a implementação de políticas de largo alcance para o enfrentamento do problema.<br>A cross-sectional study was conducted in a representative sample of 426 randomly selected first graders (ages 6 to 10 years) from public schools in Maceió, State of Alagoas, Brazil. The aim was to determine the prevalence of anemia, as well as its association with growth retardation. Data were collected from May to July 2000, and determination of hemoglobin (HGB) employed an STKS Coulter counter. Two cut-off points were used to classify anemia, both established by the World Health Organization: HGB < 11.5g/dl and HGB < 12.0g/dl. The indicators height/age (H/A), weight/age (W/A), and weight/height (W/H) below -2.0 standard deviations from the NCHS reference were diagnosed as growth retardation. Prevalence of anemia was 9.9% when HGB < 11.5g/dl was used, and 25.4% when the cut-off point was HGB < 12.0g/dl. Growth retardation was detected in 6.2% of children according to H/A, 4.0% for W/A, and 3.0% for W/H. There was no statistically significant association between the variables in the study. These findings confirm results of previous surveys where prevalence of anemia was much higher than that of growth retardation. The severe consequences of anemia in this age group justify the implementation of broad public policies to overcome this nutritional deficiency