GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Medicine  (4)
  • XA 33650  (4)
Material
Publisher
Language
Years
FID
Subjects(RVK)
  • Medicine  (4)
RVK
  • XA 33650  (4)
  • 1
    In: British Journal of Clinical Pharmacology, Wiley, Vol. 86, No. 8 ( 2020-08), p. 1519-1527
    Abstract: Chinese children are more susceptible to the development of thiopurine‐induced leukopenia compared with Caucasian populations. The aim of our study was to establish a 6‐mercaptopurine (6‐MP) dose–concentration–response relationship through exploration of pharmacogenetic factors involved in the thiopurine‐induced toxicities in Chinese paediatric patients afflicted by acute lymphoblastic leukaemia (ALL). Methods Blood samples were obtained from ALL children treated with 6‐MP. We determined the metabolite steady‐state concentrations of 6‐MP in red blood cells (RBCs) by using high‐performance liquid chromatography. Pharmacogenetic analysis was carried out on patients' genomic DNA using the MassArray genotyping platform. Results Sixty children afflicted by ALL who received 6‐MP treatment were enrolled in this study. The median concentration of 6‐thioguanine in patients afflicted by leukopenia was 235.83 pmol/8 × 10 8 RBCs, which was significantly higher than for patients unafflicted by leukopenia (178.90 pmol/8 × 10 8 RBCs; P = 0.029). We determined the population special target 6‐thioguanine threshold to have equalled 197.50 pmol/8 × 10 8 RBCs to predict leukopenia risk in Chinese paediatric patients afflicted by ALL. Among 36 candidate single nucleotide polymorphisms, our results indicated that NUDT15 (rs116855232) and IMPDH1 (rs2278293) were correlated with a 5.50‐fold and 5.80‐fold higher risk of leukopenia, respectively. MTHFR rs1801133 variants were found to have had a 4.46‐fold significantly higher risk of hepatotoxicity vs wild‐type genotype. Conclusion Our findings support the idea that predetermination of genotypes and monitoring of thiopurine metabolism for Chinese paediatric patients afflicted by ALL is necessary to effectively predict the efficacy of treatments and to minimize the adverse effects of 6‐MP maintenance therapy.
    Type of Medium: Online Resource
    ISSN: 0306-5251 , 1365-2125
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 1498142-7
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    Wiley ; 2008
    In:  British Journal of Clinical Pharmacology Vol. 66, No. 2 ( 2008-08), p. 240-246
    In: British Journal of Clinical Pharmacology, Wiley, Vol. 66, No. 2 ( 2008-08), p. 240-246
    Type of Medium: Online Resource
    ISSN: 0306-5251 , 1365-2125
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2008
    detail.hit.zdb_id: 1498142-7
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: British Journal of Clinical Pharmacology, Wiley, Vol. 87, No. 12 ( 2021-12), p. 4823-4830
    Abstract: To assess association between quetiapine treatment and risk of new‐onset hypothyroidism in schizophrenia patients. Methods We conducted a retrospective cohort study in a tertiary hospital in China between January 2016 and December 2018. Schizophrenia patients with normal thyroid tests at admission were included. Hypothyroidism, which was defined as thyroid‐stimulating hormone 〉 4.20 mU/L and free thyroxine 〈 12.00 pmol/L, or on L‐thyroxine prescriptions, was the outcome measure, and quetiapine treatment between admission and subsequent thyroid test was the exposure measure of this study. Adjusted relative risks and 95% confidence intervals were used to assess the independent association of quetiapine treatment with risk of new‐onset hypothyroidism. The dose–response association was further analysed by 3 quetiapine doses: low (≤ 〈 =0.2 g/d), medium (0.2–0.6 g/d), and high ( 〉 0.6 g/d). Results A total of 2022 eligible patients were included in the final analysis. Sixty patients (15.0%) in the quetiapine group developed hypothyroidism, while 56 patients (3.5%) in the nonquetiapine group developed hypothyroidism. Relative risk (95% confidence interval) of developing hypothyroidism for quetiapine use was 4.01 (2.86–5.64) after adjusting for several potential confounding factors. A strong dose–response association between quetiapine use and risk of developing hypothyroidism was observed: adjusted relative risks (95% confidence intervals) were 1.00 (0.25–2.59), 4.22 (2.80–6.25) and 5.62 (3.66–8.38), respectively, for low‐, medium‐ and high‐dose quetiapine, as compared with no quetiapine. Conclusion Acute phase quetiapine treatment for schizophrenia patients was strongly associated with increased risk of developing new‐onset hypothyroidism, with a clear dose–response association.
    Type of Medium: Online Resource
    ISSN: 0306-5251 , 1365-2125
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 1498142-7
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: British Journal of Clinical Pharmacology, Wiley, Vol. 88, No. 1 ( 2022-01), p. 214-225
    Abstract: Hypothyroxinaemia could be easily neglected if attention is paid only to patients with elevated thyroid‐stimulating hormone. We aimed to assess the association between mirtazapine use and hypothyroxinaemia in patients affected by major depressive disorder. Methods We conducted a retrospective cohort study in the Second Affiliated Hospital of Xinxiang Medical University between January 2016 and December 2018. Patients affected by major depression disorder and admitted to the hospital for treatment during the study period and who had thyroid tests at admission and after treatment were included. Mirtazapine use during hospitalization was the exposure measure and newly developed hypothyroxinaemia was as the primary outcome and structure parameters of thyroid homeostasis were the secondary outcomes of this study. Log‐binomial model was used to estimate the association between mirtazapine use and hypothyroxinaemia, after adjusting for potential confounding factors. Results A total of 220 eligible patients were included in the final analysis. The incidence of hypothyroxinaemia in patients who used mirtazapine was higher (37.5%) than those patients who did not use (19.7%). The relative risk of developing hypothyroxinaemia was 1.70 (95% confidence interval: 1.21–2.43) for mirtazapine use, after adjusting for confounding factors. The degree of reduction in thyroid feedback quantile‐based index in mirtazapine group was significantly greater than that in nonmirtazapine group. Conclusion Mirtazapine use was associated with the increased risk of developing hypothyroxinaemia. The underlying mechanism may be involved the changed central set point of thyroid homeostasis, in which pituitary was in a possibly impaired sensitivity to the lower level of thyroid hormones.
    Type of Medium: Online Resource
    ISSN: 0306-5251 , 1365-2125
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1498142-7
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...