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  1. AU="la Cour, Jeppe L"
  2. AU="Haraldsdóttir, Hulda S"
  3. AU="Novak, Rene"
  4. AU="Rolke, Roman"
  5. AU="Pérez, Adriana"
  6. AU="Yucel, Kamile"
  7. AU=Kumar Arun
  8. AU="Zou, Bin"
  9. AU="Krass, Stefan"
  10. AU="Patrick Connerton"
  11. AU="Lai, Jiaying"
  12. AU=Kalra Mannudeep K AU=Kalra Mannudeep K
  13. AU=Wright Zachary AU=Wright Zachary
  14. AU="Brakensiek, Stefan"
  15. AU="Akilov, Oleg"
  16. AU="Pavlish, April"
  17. AU="Kim, Joonhee"
  18. AU="Napp, Adriane"
  19. AU="Alchin, David Rhys"
  20. AU="Chenxiang Xi"
  21. AU="Alatawi, Mohammed Naif"
  22. AU="Jacquemet, Elise"
  23. AU="Cappelleri, Joseph C"
  24. AU="Frank, Samuel A"
  25. AU="Srensen, Henrik Toft"
  26. AU="Matteo Tosato"

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  1. Artikel: Effects of levothyroxine substitution therapy on hunger and food intake in individuals with hypothyroidism.

    Medici, Bjarke R / Nygaard, Birte / la Cour, Jeppe L / Krakauer, Martin / Brønden, Andreas / Sonne, Mette P / Holst, Jens J / Rehfeld, Jens F / Vilsbøll, Tina / Faber, Jens / Knop, Filip K

    Endocrine connections

    2023  Band 12, Heft 10

    Abstract: Context: In individuals with hypothyroidism and overweight, levothyroxine substitution therapy is often expected to cause weight loss due to its effect on resting energy expenditure. However, despite levothyroxine-induced enhancement of resting energy ... ...

    Abstract Context: In individuals with hypothyroidism and overweight, levothyroxine substitution therapy is often expected to cause weight loss due to its effect on resting energy expenditure. However, despite levothyroxine-induced enhancement of resting energy expenditure, fat mass loss is rarely seen after levothyroxine substitution therapy. The mechanism behind this conundrum is unknown.
    Aim: The aim of the study was to assess the effect of levothyroxine therapy on hunger sensations and ad libitum food intake in individuals with hypothyroidism.
    Design and setting: Prospective cohort study of 18 newly diagnosed hypothyroid women (thyroid-stimulating hormone (TSH) >10 mU/L). Participants were investigated at diagnosis, after normalization of TSH (<4.0 mU/L), and after 6 months of successful treatment. Eighteen age and body mass index-matched healthy controls were also included.
    Intervention: Hypothyroid individuals were treated with levothyroxine according to European Thyroid Association guidelines.
    Main outcomes: Changes in hunger sensation were assessed using visual analog scales (cm) before and during a standardized mixed meal test, and food intake was measured during a subsequent ad libitum meal (g).
    Results: After 6 months of levothyroxine therapy, mean resting energy expenditure was increased by 144 kcal/day (10%) (P < 0.001). Weight loss was comprised of 0.8 kg fat-free mass while fat mass remained unchanged. Fasting hunger sensation increased from a mean of 4.5 (s.d. 2.2) cm to 5.5 (s.d. 2.2) cm (P = 0.047). The numerical increase in ad libitum meal intake did not reach statistical significance.
    Conclusion: Our data suggest that levothyroxine-induced hunger may be a culprit in the lack of fat mass loss from levothyroxine therapy.
    Sprache Englisch
    Erscheinungsdatum 2023-09-19
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2668428-7
    ISSN 2049-3614
    ISSN 2049-3614
    DOI 10.1530/EC-23-0314
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Hypothyroid women have persistently higher oxidative stress compared to healthy controls.

    Riis, Kamilla R / Larsen, Camilla B / Medici, Bjarke R / Jensen, Christian Z / Winther, Kristian H / Larsen, Emil L / Ellervik, Christina / la Cour, Jeppe L / Hegedüs, Laszlo / Brix, Thomas H / Poulsen, Henrik E / Knop, Filip K / Nygaard, Birte / Bonnema, Steen J

    European thyroid journal

    2023  Band 12, Heft 6

    Abstract: Objective: Some studies suggest that hypothyroidism is associated with increased oxidative stress. Urinary excretion of 8-oxo-7,8-dihydroguanosine (8-oxoGuo) and 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) represents whole-body RNA and DNA oxidation, ... ...

    Abstract Objective: Some studies suggest that hypothyroidism is associated with increased oxidative stress. Urinary excretion of 8-oxo-7,8-dihydroguanosine (8-oxoGuo) and 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) represents whole-body RNA and DNA oxidation, respectively. These biomarkers have only been explored sparsely in patients with thyroid disorders.
    Methods: In 45 Danish women with newly diagnosed hypothyroidism, we compared 8-oxoGuo and 8-oxodG before or shortly after initiating levothyroxine with the excretion rates at euthyroidism. We also compared the excretion of 8-oxoGuo and 8-oxodG in the patients after restored euthyroidism with 18 healthy control subjects.
    Results: Compared with baseline, none of the biomarkers changed significantly in the patients after becoming euthyroid. The geometric mean of 8-oxoGuo was 1.63 (95% CI: 1.49-1.78) nmol/mmol creatinine at baseline and 1.67 nmol/mmol at euthyroidism (95% CI: 1.53-1.83) (P = 0.39), while that of 8-oxodG was 1.28 nmol/mmol creatinine at baseline (95% CI: 1.14-1.44) and 1.32 nmol/mmol at euthyroidism (95% CI: 1.18-1.48), respectively (P = 0.47). The relative mean differences were 0.97 (95% CI: 0.91-1.04) for 8-oxoGuo and 0.97 (95% CI: 0.88-1.06) for 8-oxodG. At baseline, multiple linear regression revealed a positive association between free thyroxine and both biomarkers (8-oxoGuo, P < 0.001; 8-oxodG, P = 0.04). Furthermore, 8-oxoGuo was positively associated with age (P = 0.04) and negatively associated with thyrotropin (P = 0.02). In the control group, the geometric mean of 8-oxoGuo was 1.23 nmol/mmol creatinine (95% CI: 1.07-1.42), while that of 8-oxodG was 1.04 nmol/mmol creatinine (95% CI: 0.88-1.23). Thus, compared with control subjects, euthyroid patients showed a significantly higher level of both 8-oxoGuo (P < 0.001) and 8-oxodG (P = 0.03).
    Conclusion: In hypothyroid women, no significant effect of levothyroxine treatment on the oxidative stress biomarkers 8-oxoGuo and 8-oxodG could be demonstrated. However, the excretion of these biomarkers was significantly higher than in healthy controls.
    Mesh-Begriff(e) Humans ; Female ; 8-Hydroxy-2'-Deoxyguanosine/urine ; Thyroxine ; Creatinine/urine ; Oxidative Stress/genetics ; Biomarkers/urine ; Hypothyroidism/drug therapy
    Chemische Substanzen 8-Hydroxy-2'-Deoxyguanosine (88847-89-6) ; Thyroxine (Q51BO43MG4) ; Creatinine (AYI8EX34EU) ; Biomarkers
    Sprache Englisch
    Erscheinungsdatum 2023-11-03
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2659767-6
    ISSN 2235-0802 ; 2235-0640
    ISSN (online) 2235-0802
    ISSN 2235-0640
    DOI 10.1530/ETJ-23-0167
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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