Impact of JAK2V617F mutational on haematologic features in Sudanese patients with essential thrombocythemia and thrombotic risk assessment

Objective: We correlated selected haematological parameters in Sudanese essential thrombocythemia (ET) patients based on their homozygous/heterozygous JAK2V617F genotype, as well as the application of thrombotic risk assessment using different thrombotic risk scoring models. Methods: In this single-center study, we evaluated 60 patients with ET at the time of the diagnosis without any prior treatment. Amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) technique was used to determine JAK2V617F mutation status. Complete blood count was evaluated using the Sysmex analyzer. Furthermore, the thrombotic risk assessment of ET patients using different thrombotic risk scoring models was applied. Results: The JAK2V617F mutation was detected in 29/60 patients (48.3%), of whom 23 (38.3% of total) were heterozygous and 6 (10.0%) were homozygous. Compeered to JAK2 wild-type or JAK2 heterozygous patients, JAK2 homozygous patients for JAK2V617F mutation were associated with older age(p < 0.05), significantly higher mean leukocytes count (P =0.001), significantly lower Hb concentration (p < 0.05), and splenomegaly (p < 0.05), while the mean of the platelet counts was slightly higher, although not reached a significant level. We also found two patients who developed thrombotic events throughout follow-up and were initially classified as a low-risk category in the traditional classification. One of them with age < 60 years, hypertension, and JAK2 homozygosity but without thrombosis history, was allocated in a high-risk category by IPSET-t and r- IPSET-t scores. The second patient was stratified in a low-risk category by all scoring models with age < 60 years, hypertension, leukocytosis, unmutated JAK2, and without a history of thrombosis. Conclusions: The JAK2 V617F homozygosity correlated with older age, higher leukocyte count, lower Hb concentration, and a higher risk of thrombosis in Sudanese ET patients. Evaluation of hypertension and identification of JAK2 V617F homozygosity at diagnosis of ET might give the clinician more meaningful prognostic information and so improve the therapeutic management

Disorders of Transepidermal Elimination

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65203/1/j.1365-4362.1985.tb05799.x.pd

Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease

Metabolic associated fatty liver disease (MAFLD) is the most prevalent liver disease in Western nations, with high heritability. A recent study of Japanese patients with the disease suggested that TLL1 rs17047200 is associated with fibrosis; whether a similar association is observed in Caucasian patients with MAFLD is unknown. We investigated the association of the TLL1 rs17047200 polymorphism with liver fibrosis in a cohort of Caucasian patients with MAFLD (n = 728). We also investigated whether TLL1 expression is altered during liver injury in humans, in murine models of fibrosis, and in in-vitro. While TLL1 expression is upregulated in the liver of humans with MAFLD and in mice, the rs17047200 variant was not associated with fibrosis or any other histological features, or with hepatic TLL1 expression. In conclusion, the TLL1 rs17047200 variant is not a risk variant for fibrosis in Caucasian patients with MAFLD. However, TLL1 could be involved in the pathogenesis of liver fibrosis

A critical systematic review and meta-analyses of risk factors for fertility problems in a globalized world

Globally fertility awareness efforts include well-established risk factors (RFs) for fertility-problems. However, risks disproportionately affecting females in the Global South are neglected. To address this gap, we conducted systematic reviews and meta-analysis of relevant RFs, to examine association between RFs and fertility-problems. We searched Medline, Embase, Cochrane library, regional databases and key organizational websites. Three authors screened and extracted data independently. We included studies assessing exposure to risk (clinical, community-based samples) and excluded studies without control groups. Outcome of interest was fertility-problems (inability to achieve pregnancy, live-birth, neonatal death). Newcastle-Ottawa Scale used to assess study quality. We identified 3843 studies, and included 62 (58 in meta-analyses, 115,810 patients). Results revealed nine-fold risk of inability to become pregnant in genital-tuberculosis (OR=8.91, CI=1.89-42.12), almost threefold in HIV (OR=2.93, CI=1.95-4.42) and bacterial-vaginosis (OR=2.81, CI=1.85-4.27). Twofold risk of tubal-factor infertility in Female Genital Mutilation/Cutting–Type II/III (OR=2.06, CI=1.03-4.15) and post-natal mortality in consanguinity (stillbirth, OR=1.28, CI=1.04-1.57; neonatal death, OR=1.57, CI=1.22-2.02). It appears RFs impacted reproductive processes through multiple pathways. Health promotion encompassing relevant health indicators could enhance prevention and early detection of fertility-problems in the Global South and disproportionately affected populations. The multifactorial risk-profile reinforces the need to place fertility within global health initiatives

Elevated blood lead levels are associated with reduced risk of malaria in Beninese infants

Introduction Elevated blood lead levels (BLL) and malaria carry an important burden of disease in West Africa. Both diseases might cause anemia and they might entail long-term consequences for the development and the health status of the child. Albeit the significant impact of malaria on lead levels described in Nigeria, no evaluation of the effect of elevated BLL on malaria risk has been investigated so far. Materials and Methods Between 2010 and 2012, blood lead levels of 203 Beninese infants from Allada, a semi-rural area 50km North from Cotonou, were assessed at 12 months of age. To assess lead levels, blood samples were analyzed by mass spectrometry. In parallel, clinical, microbiological and hematological data were collected. More precisely, hemoglobin, serum ferritin, CRP, vitamin B12, folate levels, and Plasmodium falciparum parasitemia were assessed and stool samples were also analyzed. Results At 12 months, the mean BLL of infants was 7.41 μg/dL (CI: 65.2; 83), and 128 infants (63%) had elevated blood lead levels, defined by the CDC as BLL>5 μg/dL. Lead poisoning, defined as BLL>10 μg/dL, was found in 39 infants (19%). Twenty-five infants (12.5%) had a positive blood smear at 12 months and 144 infants were anemic (71%, hemoglobin<110 g/L). Elevated blood lead levels were significantly associated with reduced risk of a positive blood smear (AOR = 0.38, P-value = 0.048) and P. falciparum parasite density (beta-estimate = -1.42, P-value = 0.03) in logistic and negative binomial regression multivariate models, respectively, adjusted on clinical and environmental indicators. Conclusion Our study shows for the first time that BLL are negatively associated with malarial risk considering other risk factors. Malaria is one of the main causes of morbidity and mortality in infants under 5 years worldwide, and lead poisoning is the 6th most important contributor to the global burden of diseases measured in disability adjusted life years (DALYs) according to the Institute of Health Metrics. In conclusion, due to the high prevalence of elevated BLL, health interventions should look forward to minimize the exposure to lead to better protect the population in West Africa

Campylobacter Infection as a Trigger for Guillain-Barré Syndrome in Egypt

BACKGROUND: Most studies of Campylobacter infection triggering Guillain-Barré Syndrome (GBS) are conducted in western nations were Campylobacter infection and immunity is relatively rare. In this study, we explored Campylobacter infections, Campylobacter serotypes, autoantibodies to gangliosides, and GBS in Egypt, a country where Campylobacter exposure is common. METHODS: GBS cases (n = 133) were compared to age- and hospital-matched patient controls (n = 374). A nerve conduction study was performed on cases and a clinical history, serum sample, and stool specimen obtained for all subjects. RESULTS: Most (63.3%) cases were demyelinating type; median age four years. Cases were more likely than controls to have diarrhea (29.5% vs. 22.5%, Adjusted Odds Ratio (ORa) = 1.69, P = 0.03), to have higher geometric mean IgM anti-Campylobacter antibody titers (8.18 vs. 7.25 P<0.001), and to produce antiganglioside antibodies (e.g., anti-Gd1a, 35.3 vs. 11.5, ORa = 4.39, P<0.0001). Of 26 Penner:Lior Campylobacter serotypes isolated, only one (41:27, C. jejuni, P = 0.02) was associated with GBS. CONCLUSIONS: Unlike results from western nations, data suggested that GBS cases were primarily in the young and cases and many controls had a history of infection to a variety of Campylobacter serotypes. Still, the higher rates of diarrhea and greater antibody production against Campylobacter and gangliosides in GBS patients were consistent with findings from western countries