Serum zinc reference intervals and its relationship with dietary, functional, and biochemical indicators in 6- to 9-year-old healthy children.

BACKGROUND: Zinc is an important cause of morbidity, particularly among young children. The dietary, functional, and biochemical indicators should be used to assess zinc status and to indicate the need for zinc interventions. OBJECTIVE: The purpose of this study was to determine the zinc status and reference intervals for serum zinc concentration considering dietary, functional, and biochemical indicators in apparently healthy children in the Northeast Region of Brazil. DESIGN: The cross-sectional study included 131 healthy children: 72 girls and 59 boys, aged between 6 and 9 years. Anthropometric assessment was made by body mass index (BMI) and age; dietary assessment by prospective 3-day food register, and an evaluation of total proteins was performed. Zinc in the serum samples was analyzed in triplicate in the same assay flame, using atomic absorption spectrophotometry. RESULTS: With respect to dietary assessment, only the intake of fiber and calcium was below the recommendations by age and gender. All subjects were eutrophic according to BMI and age classification. Zinc intake correlated with energy (p=0.0019), protein (p=0.0054), fat (p<0.0001), carbohydrate (p=0.0305), fiber (p=0.0465), calcium (p=0.0006), and iron (p=0.0003) intakes. Serum zinc correlated with protein intake (p=0.0145) and serum albumin (p=0.0141), globulin (p=0.0041), and albumin/globulin ratio (p=0.0043). Biochemical parameters were all within the normal reference range. Reference intervals for basal serum zinc concentration were 0.70-1.14 µg/mL in boys, 0.73-1.17 µg/mL in girls, and 0.72-1.15 µg/mL in the total population. CONCLUSIONS: This study presents pediatric reference intervals for serum zinc concentration, considering dietary, functional, and biochemical indicators, which are useful to establish the zinc status in specific groups. In this regard, there are few studies in the literature conducted under these conditions, which make it an innovative methodology.

Sexual dysfunction in obese women is more affected by psychological domains than that of non-obese.

PURPOSE: To compare differences in the occurrence and changed domains of sexual dysfunction in obese and non-obese Brazilian women. METHODS: Female Sexual Function Index, based on six domains, to investigate 31 sexual dysfunction incidence for obese compared to 32 non-obese women, was used. Statistical analysis using ANOVA and MANOVA were performed to compare total scores of Female Sexual Function Index among groups and to identify the differences among domains, Student t -test was used. Statistical significant level was established for all tests for p<0.05. RESULTS: No difference in female sexual dysfunction frequency between obese (25.8%) and non-obese women (22.5%) was found. However, an important distinction in which aspects of sexual life were affected was found. While the obese group was impaired in three domains of sexual life (desire, orgasm, and arousal), in the control group five aspects were dysfunctional (desire, orgasm, arousal, pain and lubrication). Future research exploring psychological outcomes in obese females, such as body image and measures of positive and negative effect, might better characterize the female sexual dysfunction in this group. CONCLUSIONS: Obesity does not appear to be an independent factor for allow quality of female sexual life. However, disturbance associated to obesity indicates a low frequency of disorder in physical domains, suggesting that psychological factors seem to be mainly involved in the sexual dysfunction in obese women.

Sexual dysfunction in obese women is more affected by psychological domains than that of non-obese / Disfunção sexual em mulheres obesas é mais afetada por domínios psicológicos do que nas não obesas

Abstract PURPOSE: To compare differences in the occurrence and changed domains of sexual dysfunction in obese and non-obese Brazilian women. METHODS: Female Sexual Function Index, based on six domains, to investigate 31 sexual dysfunction incidence for obese compared to 32 non-obese women, was used. Statistical analysis using ANOVA and MANOVA were performed to compare total scores of Female Sexual Function Index among groups and to identify the differences among domains, Student t -test was used. Statistical significant level was established for all tests for p<0.05. RESULTS: No difference in female sexual dysfunction frequency between obese (25.8%) and non-obese women (22.5%) was found. However, an important distinction in which aspects of sexual life were affected was found. While the obese group was impaired in three domains of sexual life (desire, orgasm, and arousal), in the control group five aspects were dysfunctional (desire, orgasm, arousal, pain and lubrication). Future research exploring psychological outcomes in obese females, such as body image and measures of positive and negative effect, might better characterize the female sexual dysfunction in this group. CONCLUSIONS: Obesity does not appear to be an independent factor for allow quality of female sexual life. However, disturbance associated to obesity indicates a low frequency of disorder in physical domains, suggesting that psychological factors seem to be mainly involved in the sexual dysfunction in obese women.

Resumo OBJETIVO: Comparar as diferenças na incidência de disfunção sexual nos seis diferentes domínios de mulheres brasileiras obesas e não obesas. MÉTODOS: Foi usado o Female Sexual Function Index , que discrimina seis domínios de disfunção, para investigar a incidência de disfunção sexual em 31 mulheres obesas e 32 mulheres não obesas. Foi realizada análise estatística utilizando ANOVA e MANOVA para comparar os escores totais doFemale Sexual Function Index entre os grupos, bem como empregado o teste t para identificar as diferenças relacionadas aos domínios. O nível de significância estatística estabelecido para todos os testes foi de p<0,05. RESULTADOS: Não foi encontrada diferença significante nas diferentes incidências de disfunção sexual feminina entre o grupo de pacientes obesas (25,8%) e o grupo de não obesas (22,5%). Contudo, foi evidenciada uma importante distinção em quais aspectos da vida sexual foram afetados nos dois grupos. Enquanto as mulheres obesas foram impactadas em apenas três domínios subjetivos do Female Sexual Function Index (desejo, orgasmo e excitação), o grupo controle apresentou disfunção em cinco aspectos (desejo, orgasmo, excitação, dor e lubrificação). Pesquisas futuras explorando aspectos psicológicos em mulheres obesas, como a avaliação da autoimagem corporal e seus aspectos negativos ou positivos sobre as pacientes, deverão auxiliar na melhor caracterização da disfunção sexual feminina neste grupo. CONCLUSÕES: A obesidade não parece constituir um fator de risco independente para uma baixa qualidade de vida sexual feminina. Contudo, as disfunções associadas à obesidade foram menos evidenciadas em domínios fisiológicos, sugerindo que aspectos psicológicos parecem estar primariamente envolvidos na etiologia da disfunção sexual de mulheres obesas.

Association between habitual sleep duration and blood pressure and clinical implications: a systematic review.

UNLABELLED: Elucidation of the association between short sleep duration and elevated blood pressure has implications for assessing and managing hypertension in adults. OBJECTIVE: To assess the relationship between sleep duration and blood pressure, and its role in the etiology of hypertension. METHODS: On a systematic search from MEDLINE, EMBASE, CINAHL, PEDro, PsychINFO and grey literature were included articles with participants over 18 years, reported sleep duration, measured blood pressure or diagnosed hypertension, and the relationship between sleep duration and blood pressure was analyzed. RESULTS: Of 2522 articles initially identified, 11 studies met the inclusion criteria. Sample sizes ranged from 505 to 8860 (aged ≥ 20-98 years). Five studies (aged ≥ 58-60 years) determined that sleep duration and blood pressure were unrelated. In younger adults, five studies reported an association between short sleep duration and hypertension before adjustment for confounding variables; only the findings from one study remained significant after adjustment. Two studies supported a sex association; women who sleep less than 5-6 h nightly are at greater risk of developing hypertension. CONCLUSION: Sleep duration and blood pressure are associated in both women and adults under 60 years. Controlled studies are needed to elucidate confounding factors and the degree to which sleep profiles could augment diagnosis of hypertension and sleep recommendations to prevent or manage hypertension.

Influence of neck circumference on respiratory endurance and muscle strength in the morbidly obese.

BACKGROUND: Respiratory function decline has been reported mainly in the morbidly obese. Little is known about the influence of adiposity pattern on the ability to generate strength in respiratory muscles. This study evaluated strength and respiratory endurance in the morbidly obese in preoperative bariatric surgery to determine if such variables were affected by different anthropometric markers (body mass index (BMI), waist-hip ratio (WHR), and neck circumference (NC)). METHODS: We evaluated 39 adult and young obese patients of both sexes, with no respiratory or heart diseases. Standard pulmonary function tests and static respiratory muscle strength (maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP)) and endurance (maximum voluntary ventilation (MVV)) were measured in relation to sex and groups (WHR > 0.95 and WHR < 0.95; NC > 43 and NC < 43). RESULTS: Thirty-nine obese patients (28 women), aged 36.9 + 11.9 years, BMI 49.3 + 5.1 kg/m², WHR 0.96 + 0.07, and NC 44.1 + 4.2 cm, took part in the study Standard pulmonary function tests and respiratory muscle strength were within normal parameters, except MVV (<80%). Obese with NC ≥ 43 cm (n = 22) have greater respiratory muscle strength and less endurance, MEP (p = 0.031) and MVV (p = 0.018). Abdominal adiposity (n = 19) does not seem to affect respiratory muscle strength. A positive correlation was observed only between NC and PEF (r = 0.392, p = 0.014) and marginally between NC and MVV (r = 0.308, p = 0.056). CONCLUSION: Although adiposity patterns did not affect inspiratory muscle strength, neck adiposity was associated lower respiratory muscle endurance.

Modulação pela progesterona da sensibilidade dolorosa a estímulos mecânicos e isquêmicos em mulheres saudáveis e jovens / Modulation by progesterone of pain sensitivity to mechanical and ischemic stimuli in young and healthy women

OBJETIVO: investigar a relação entre percepção da dor (limiar e tolerância à dor experimental em resposta à isquemia e à pressão) em mulheres jovens e saudáveis com os níveis séricos dos hormônios sexuais femininos (estradiol e progesterona). MÉTODOS: 18 voluntárias participaram deste estudo durante três ciclos menstruais consecutivos. Para mensuração das respostas dolorosas aos estímulos algésicos de pressão e isquemia, utilizaram-se um algômetro de pressão e dinamômetro manual, respectivamente. Foram realizadas coletas de sangue para dosagem hormonal e de variáveis dolorosas durante três ciclos menstruais consecutivos, os quais foram caracterizados com base no registro da temperatura oral diária, diário dos ciclos menstruais contendo início e fim de cada ciclo e nos níveis plasmáticos de estradiol e progesterona. As médias aferidas para as variáveis algésicas foram comparadas pela análise de variância (ANOVA) com pós-teste de Tukey-Kramer entre as fases do ciclo menstrual (folicular, periovulatória, luteal inicial, luteal tardia e menstrual). Para o estudo da correlação entre as variáveis algésicas e hormonais, utilizou-se o teste de Pearson. A significância estatística foi definida pelo limite p<0,05. RESULTADOS: não foram observadas variações significativas nos parâmetros de dor entre as fases do ciclo menstrual. Todavia, foram encontradas correlações negativas significativas entre progesterona e limiar isquêmico (r=-0,23; p<0,01) e tolerância à pressão (r=-0,23; p<0,01) na fase luteal inicial. CONCLUSÕES: estes resultados indicam que o aumento dos níveis de progesterona estão relacionados à diminuição do limiar isquêmico e da tolerância à pressão, sugerindo um papel da progesterona na modulação dolorosa durante a fase luteal inicial.

PURPOSE: to investigate the relationship between pain perception (experimental pain threshold and tolerance, in response to ischemia and pressure) in young and healthy young women and female sexual hormone seric levels (estradiol and progesterone). METHODS: 18 volunteers have participated of this study, during three consecutive menstrual cycles. A pressure algometer and a manual dynamometer have been used to measure painful responses to pressure and ischemia algesic stimuli. Blood has been collected for assessment of both hormonal and painful variables, during three menstrual cycles, whose characterization was based on daily oral temperature record, a diary of the menstrual cycles with the onset and end of each cycle, and on estradiol and progesterone plasmatic levels. The average for the algesic variables measured has been compared by analysis of variance (ANOVA) and the Tukey-Kramer's post-test, among the menstrual cycle phases (follicular, periovulatory, early luteal, late luteal and menstrual). The Pearson's test has been used for correlation analysis between algesic and hormonal variables. Statistical significance has been defined as p<0.05. RESULTS: no significant change in pain parameters among the menstrual cycle phases has been observed. Nevertheless, there have been significant negative correlations between progesterone and ischemic threshold (r=-0.23; p<0.01), and pressure tolerance (r=-0.23; p<0.01) at the early luteal phase. CONCLUSIONS: these results indicate that the increase in progesterone levels correlates with a decrease of ischemic threshold and pressure tolerance, suggesting that progesterone plays a role in the pain modulation during the early luteal phase.

[Modulation by progesterone of pain sensitivity to mechanical and ischemic stimuli in young and healthy women]. / Modulação pela progesterona da sensibilidade dolorosa a estímulos mecânicos e isquêmicos em mulheres saudáveis e jovens.

PURPOSE: to investigate the relationship between pain perception (experimental pain threshold and tolerance, in response to ischemia and pressure) in young and healthy young women and female sexual hormone seric levels (estradiol and progesterone). METHODS: 18 volunteers have participated of this study, during three consecutive menstrual cycles. A pressure algometer and a manual dynamometer have been used to measure painful responses to pressure and ischemia algesic stimuli. Blood has been collected for assessment of both hormonal and painful variables, during three menstrual cycles, whose characterization was based on daily oral temperature record, a diary of the menstrual cycles with the onset and end of each cycle, and on estradiol and progesterone plasmatic levels. The average for the algesic variables measured has been compared by analysis of variance (ANOVA) and the Tukey-Kramer's post-test, among the menstrual cycle phases (follicular, periovulatory, early luteal, late luteal and menstrual). The Pearson's test has been used for correlation analysis between algesic and hormonal variables. Statistical significance has been defined as p<0.05. RESULTS: no significant change in pain parameters among the menstrual cycle phases has been observed. Nevertheless, there have been significant negative correlations between progesterone and ischemic threshold (r=-0.23; p<0.01), and pressure tolerance (r=-0.23; p<0.01) at the early luteal phase. CONCLUSIONS: these results indicate that the increase in progesterone levels correlates with a decrease of ischemic threshold and pressure tolerance, suggesting that progesterone plays a role in the pain modulation during the early luteal phase.