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High-Dose Vitamin D and Early Chronic Pancreatitis-Related Changes After Acute Pancreatitis: A Randomized Dose Controlled Trial

Parhiala, Mikael; Aronen, Anu; Ukkonen, Mika; Haukijärvi, Eija; Pappinen, Päivi; Rinta-Kiikka, Irina; Laukkarinen, Johanna (2026)

 
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High-Dose_Vitamin_D_and_Early_Chronic_Pancreatitis-Related_Changes_After_Acute_Pancreatitis.pdf (905.3Kt)
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URI
https://urn.fi/URN:NBN:fi:tuni-202602032221


Parhiala, Mikael
Aronen, Anu
Ukkonen, Mika
Haukijärvi, Eija
Pappinen, Päivi
Rinta-Kiikka, Irina
Laukkarinen, Johanna
2026

Digestive Diseases and Sciences
doi:10.1007/s10620-026-09688-x
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202602032221

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Peer reviewed
Tiivistelmä
Objectives: Chronic pancreatitis (CP) is an irreversible condition with multiple comorbidities. Pancreatic stellate cells (PCSs) are crucial in the fibrotic process in CP. PSCs have a regulating vitamin D receptor. The aim was to assess if a daily higher dose of vitamin D can prevent the progression to CP in patients after the first episode of acute pancreatitis (AP). Methods: This was a single-centre randomized placebo -controlled trial. Patients were randomized after the first episode of AP to either a daily 100 µg high-dose vitamin D (HDVD) or a 10 µg low-dose vitamin D (LDVD) groups. Follow-up included magnetic resonance imaging (MRI), laboratory tests and QoL questionnaires (QLQ-C30 and Pan26). The development of parenchymal changes possibly related to fibrosis after AP in MRI. Results: Sixty-nine patients were recruited. There was a high dropout (51%), therefore the final analysis included all patients who completed the three or two years of trial: in total 34 patients. No definitive CP cases occurred in HDVD group, while one was observed in LDVD group (p = 0.367). Less CP related findings developed during the trial in the HDVD compared to the LDVD group (n = 4 vs n = 13, p = 0.016). The HDVD patients had a significantly lower pain score than the LDVD group (p = 0.019). Vitamin D levels were significantly higher in HDVD group compared to LDVD group without adverse effects. Conclusions: HDVD after AP was linked to fewer early CP-related changes during 2–3 years of follow-up. These preliminary findings warrant confirmation in larger trials with longer observation. Long-term interventional trials are challenging in this patient group. Trial registration number: ClinicalTrials.gov: NCT02965898.
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  • TUNICRIS-julkaisut [24322]
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste
 

 

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TekijätNimekkeetTiedekunta (2019 -)Tiedekunta (- 2018)Tutkinto-ohjelmat ja opintosuunnatAvainsanatJulkaisuajatKokoelmat

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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste