The objective of this study was to analyse the survival rate and cause of death in children with systemic lupus erythematosus (SLE) during the past 30 years in Chile. A retrospective analysis was performed between 1969 and 2000 on patients attending pediatric rheumatology centres in Santiago, Chile. Survival and causes of death in 31 children followed from 1969 to 1980 fulfilling the 1982 American College of Rheumatology criteria for SLE and treated with oral steroids were compared with 50 other patients who were treated with oral steroids and an aggressive treatment of IV bolus of cyclophosphamide (38 patients) and azathioprine (12 patients). Global survival at five and 10 years follow-up for the patients studied from 1969 to 1980 was 68 and 40%, respectively. During the second study period these values were significantly improved and global survival reached 95% at five years and 90% at 10 years follow-up (P < 0.05). Survival at 10 years follow-up for patients with lupus nephropathy increased from 28% (study period 1964-1980) to 86% (study period 1984-2000). Twelve children died (38%) during the 1964-1980 study period. The causes of death were six due to kidney failure, three due to infectious conditions and another three of unknown causes. During the 1980-2000 study period mortality reached 6% (three cases), two cases died of a lupus flare-up and one case due to infection. In the last three decades, we have seen an important increase in the survival of children with SLE, especially in those patients with renal involvement. Management with immunosuppressive drugs, such as IV cyclophosphamide or azathioprine has changed the prognosis in these children. These results demonstrate that our children with SLE increased their life expectancy but are now faced with new types of morbidity because of the sequelae related to the disease itself.

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In this study, we evaluated the possibility of obtaining successive Astyanax altiparanae spawns under laboratory conditions. In order to do so, 104 specimens were randomly distributed into four boxes (10 females and 16 males each) and kept in a recirculation system at an average temperature of 29.24 ± 0.42 °C, under natural photoperiod, for 30 days. On the onset of the experiment, males and females were induced for reproduction with a 6 mg kg-1 carp pituitary extract dose. After that, ovary (for gonadosomatic index and stereological assessment) and blood samples (for steroid evaluation) were collected from eight females (two per box) at the following moments: immediately after hormonal induction (day 0) and on days 1, 6, 16 and 30 after spawning. On day 6, spawned females presented complete mature ovaries similar to those on day 0 and, in this period, we did not observe postovulatory complexes, indicating that their resorption happened very fast. Concomitantly, the steroid levels increased gradually up to day 6, which corroborated an intense vitellogenic activity in this period. This study has demonstrated that A. altiparanae females are suitable for induced spawning within six days after spawning, when kept at 29.24 ± 0.42 °C, in a system maintained with recirculated water.

Scarce genomic resources have limited the development of breeding programs for serrasalmid fish Colossoma macropomum (tambaqui) and Piaractus mesopotamicus (pacu), the key native freshwater fish species produced in South America. The main objectives of this study were to design a dense SNP array for this fish group and to validate its performance on farmed populations from several locations in South America. Using multiple approaches based on different populations of tambaqui and pacu, a final list of 29,575 and 29,612 putative SNPs was selected, respectively, to print an Axiom AFFYMETRIX (THERMOFISHER) SerraSNP array. After validation, 74.17% (n = 21,963) and 71.25% (n = 21,072) of SNPs were classified as polymorphic variants in pacu and tambaqui, respectively. Most of the SNPs segregated within each population ranging from 14,199 to 19,856 in pacu; and from 15,075 to 20,380 in tambaqui. Our results indicate high levels of genetic diversity and clustered samples according to their hatchery origin. The developed SerraSNP array represents a valuable genomic tool approaching in-depth genetic studies for these species.

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