Janusz Kazimierz Rybakowski

Prof. Dr. Janusz Kazimierz Rybakowski

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Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 1999 in Journal of Psychiatric Research
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Journal Article
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JRJanusz Kazimierz Rybakowski
Janusz Kazimierz Rybakowski
KTKatarzyna Twardowska
Katarzyna Twardowska

1 April 2001 in Bipolar Disorders
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ABAlina Borkowska
Alina Borkowska
JRJanusz Kazimierz Rybakowski
Janusz Kazimierz Rybakowski

25 November 2003 in Bipolar Disorders
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JRJanusz Kazimierz Rybakowski
Janusz Kazimierz Rybakowski
ABAlina Borkowska
Alina Borkowska
PCPiotr M Czerski
Piotr M Czerski
MSMaria Skibińska
Maria Skibińska
JHJoanna Hauser
Joanna Hauser

1 August 2017 in International Journal of Bipolar Disorders
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LTLeonardo Tondo
Leonardo Tondo
MAMaria Abramowicz
Maria Abramowicz
MAMartin Alda
Martin Alda
MBMichael Bauer
Michael Bauer
ABAlberto Bocchetta
Alberto Bocchetta
RBRoss Baldessarini
Ross Baldessarini
Concerns about potential adverse effects of long-term exposure to lithium as a mood-stabilizing treatment notably include altered renal function. However, the incidence of severe renal dysfunction; rate of decline over time; effects of lithium dose, serum concentration, and duration of treatment; relative effects of lithium exposure vs. aging; and contributions of sex and other factors all remain unclear. Accordingly, we acquired data from 12 collaborating international sites and 312 bipolar disorder patients (6142 person-years, 2669 assays) treated with lithium carbonate for 8–48 (mean 18) years and aged 20–89 (mean 56) years. We evaluated changes of estimated glomerular filtration rate (eGFR) as well as serum creatinine, urea–nitrogen, and glucose concentrations, white blood cell count, and body-mass index, and tested associations of eGFR with selected factors, using standard bivariate contrasts and regression modeling. Overall, 29.5% of subjects experienced at least one low value of eGFR ( 55; risk of ≥2 low values was 18.1%; none experienced end-stage renal failure. eGFR declined by 0.71%/year of age and 0.92%/year of treatment, both by 19% more among women than men. Mean serum creatinine increased from 0.87 to 1.17 mg/dL, BUN from 23.7 to 33.1 mg/dL, glucose from 88 to 122 mg/dL, and BMI from 25.9 to 26.6 kg/m2. By multivariate regression, risk factors for declining eGFR ranked: longer lithium treatment, lower lithium dose, higher serum lithium concentration, older age, and medical comorbidity. Later low eGFR was also predicted by lower initial eGFR, and starting lithium at age ≥ 40 years. Control data for age-matched subjects not exposed to lithium were lacking. Long-term lithium treatment was associated with gradual decline of renal functioning (eGFR) by about 30% more than that was associated with aging alone. Risk of subnormal eGFR was from 18.1% (≥2 low values) to 29.5% (≥1 low value), requiring about 30 years of exposure. Additional risk factors for low eGFR were higher serum lithium level, longer lithium treatment, lower initial eGFR, and medical comorbidity, as well as older age.

1 September 2017 in Neuropsychiatric Disease and Treatment
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DŁDorota Łojko
Dorota Łojko
JRJanusz Kazimierz Rybakowski
Janusz Kazimierz Rybakowski
The history and present status of the definition, prevalence, neurobiology, and treatment of atypical depression (AD) is presented. The concept of AD has evolved through the years, and currently, in Diagnostic and Statistical Manual of Mental Disorders (DSM), Fifth Edition, the specifier of depressive episode with atypical feature is present for both diagnostic groups, that is, depressive disorders and bipolar and related disorders. This specifier includes mood reactivity, hyperphagia, hypersomnia, leaden paralysis, and interpersonal rejection sensitivity. Prevalence rates of AD are variable, depending on the criteria, methodology, and settings. The results of epidemiological studies using DSM criteria suggest that 15%–29% of depressed patients have AD, and the results of clinical studies point to a prevalence of 18%–36%. A relationship of AD with bipolar depression, seasonal depression, and obesity has also been postulated. Pathogenic research has been mostly focused on distinguishing AD from melancholic depression. The differences have been found in biochemical studies in the areas of hypothalamic–pituitary–adrenal axis, inflammatory markers, and the leptin system, although the results obtained are frequently controversial. A number of findings concerning such differences have also been obtained using neuroimaging and neurophysiological and neuropsychological methods. An initial concept of AD as a preferentially monoamine oxidase inhibitor-responsive depression, although confirmed in some further studies, is of limited use nowadays. Currently, despite numerous drug trials, there are no comprehensive treatment guidelines for AD. We finalize the article by describing the future research perspectives for the definition, neurobiology, and treatment. A better specification of diagnostic criteria and description of clinical picture, a genome-wide association study of AD, and establishing updated treatment recommendations for this clinical phenomenon should be the priorities for the coming years.

1 February 2019 in Pharmacological Reports
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PJPaulina Jaworska-Andryszewska
Paulina Jaworska-Andryszewska
JRJanusz Kazimierz Rybakowski
Janusz Kazimierz Rybakowski