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1.
Arch Anim Nutr ; 74(6): 429-444, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32962441

ABSTRACT

This study was conducted to determine apparent total tract digestibility (ATTD) of phosphorus (P) and metabolisable energy (ME) concentrations for pigs of 32 different genotypes (n = 8 per grain species) of barley, rye, triticale and wheat. All genotypes were grown at the same location under the same field conditions and were fed to growing castrated crossbred pigs (initial body weight: 31.1 ± 6.95 kg) using a series of duplicate 3 × 3 Latin square designs. A basal ration, which was deficient in P, and 32 experimental rations containing 400 g/kg DM of the basal ration and 600 g/kg DM of the corresponding cereal grain were mixed. Pigs were kept in metabolism crates and the total collection method was used for separate faeces and urine collections with 7-d adaptation and 7-d collection periods. The mean ATTD of P was greater (p < 0.05) for wheat than for triticale, rye or barley (59.4%, 50.4%, 44.9% and 44.4%, respectively, for the mean of each grain species). Within-grain species differences (p < 0.05) among genotypes were obtained for ATTD of P of barley and triticale. The concentrations of ME of triticale and wheat were higher (p < 0.05) than that of barley and rye (16.1 and 16.2 vs. 14.9 and 14.8 MJ ME/kg DM, respectively). Differences in ME concentration among genotypes within a grain species (p < 0.05) were found for barley, triticale and wheat. No differences were found for rye. Compared to literature data the present study showed, in part, considerable differences in ATTD of P and ME concentration. These results should be taken into account for accurate pig ration formulation with regard to minimised P output and efficient use of ME. No significant relationships were detected between ATTD of P and phytic acid concentration or phytase activity in the grain genotypes in this study.


Subject(s)
Digestion , Edible Grain/genetics , Energy Metabolism , Genotype , Phosphorus/physiology , Sus scrofa/physiology , Animal Nutritional Physiological Phenomena , Animals , Hordeum/genetics , Secale/genetics , Triticale/genetics , Triticum/genetics
2.
Arch Gynecol Obstet ; 296(2): 231-240, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28624987

ABSTRACT

PURPOSE: This is the first study to determine the cytomegalovirus (CMV) seronegativity rate for women of childbearing age in Saxony-Anhalt and to determine the prevalence of clinically relevant congenital CMV (cCMV) infection in Central Germany, because there are no valid data available. METHODS: The retrospective study was undertaken between January 2005 and December 2015. For the first time in Germany, the following seven data sources were used to analyze the prevalence of clinically relevant cCMV infection and the rate of CMV seronegative women of childbearing age: CMV Screening in maternity unit, University Women's Hospital, Social Paediatrics Centre (SPC), Malformation Monitoring Centre (MMC), Newborn Hearing Screening (NHS), Neonatal Intensive Care Unit (NICU), and In-house Doctor Department. Key parameters were anti-CMV IgG and IgM, CMV PCR of urine, and clinically relevant symptoms caused by CMV. RESULTS: Between 46 and 52% of women of childbearing age were CMV seronegative. The prevalence of clinically relevant cCMV infection was between 0.008 and 0.04%. CONCLUSIONS: The CMV seronegativity rate of women of childbearing age was confirmed to be in the middle range of estimated data from other sources in Germany. Data from the NICU, SPC, NHS, and MMC show the prevalence of clinically relevant cCMV infection. The risk of all cCMV infections is underestimated. Thus, the true prevalence of clinically relevant and subclinical cCMV infections is >0.04%.


Subject(s)
Cytomegalovirus Infections/congenital , Cytomegalovirus Infections/epidemiology , Cytomegalovirus/isolation & purification , Adult , Cytomegalovirus/immunology , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/virology , Female , Germany/epidemiology , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Neonatal Screening , Polymerase Chain Reaction , Prevalence , Retrospective Studies , Risk
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