Therefore it is unconceivable that sex interacted with pitch identification due to different perception thresholds.
Sex interacted with age (P=0.003) and subsite (P=0.002) such that male predominance decreased with age for both subsites.
However, sex did not interact with baseline glycemic control in the prediction of month-6 depressive symptoms (P = 0.946), nor did sex interact with baseline depressive symptoms in the prediction of month-6 glycemic control (P = 0.727).
It was hypothesized that age and sex interact in modulating cerebrovascular reactivity to vasopressin (VP) by altering the role of prostanoids in vascular function.
The evidence presented here indicates that sex interacts with disease to precipitate depression whether the disease is neural (as in epilepsy and AD) or somatic (e.g., cancer and cardiovascular disease) in origin.
However, our results suggest that weight and sex interact and show a correlation with antibody prevalence in host populations, as does age, so that heavier, older males are most likely to be LCMV positive.
Sex interacted with occupation for red and processed meat intake and with education for red and processed meat intake, demonstrating heterogeneous gradients for these particular indicators and food groups.
Thus, in the present studies, the central hypothesis tested is that age and sex interact in modulating cerebrovascular reactivity to vasopressin (VP) by altering the role of prostanoids in vascular function.
Thus, it is important to determine how age and sex interact in the regulation of cerebrovascular prostanoid production and the enhancement of both vasoconstriction and hemostasis, and how these mechanisms may differ between males (M) and F with age.
Understanding how contexts (such as social and physical environments) and characteristics of the individual (such as age, race, and sex) interact to influence health appears to be an important step in designing effective health policies.
Sex interacts with psychosis in three ways: onsets of schizophrenia are earlier (by a mean of 3 4 years) and outcome is worse in males [Penrose, 1991]; later onsets for example, of schizoaffective and affective illness show an increase in females with a clear excess among late-onset paraphrenic psychoses.
