Page last updated: 2024-11-13

1 alpha,24-dihydroxyvitamin d3

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

## 1α,24-Dihydroxyvitamin D3: A Key Player in Vitamin D Metabolism

1α,24-Dihydroxyvitamin D3, also known as **calcitriol**, is the **active form** of vitamin D3 (cholecalciferol). This form of vitamin D is produced in the kidneys through a series of enzymatic reactions.

**Importance in Research:**

1α,24-Dihydroxyvitamin D3 is vital for research because it plays a crucial role in various biological processes, including:

* **Calcium and Phosphate Homeostasis:** Calcitriol regulates the absorption of calcium and phosphate from the gut, essential for bone health and mineral metabolism. It also helps maintain healthy blood calcium levels.
* **Immune System Modulation:** Calcitriol is involved in regulating immune responses, influencing the differentiation and function of immune cells. This makes it a potential target for research on autoimmune diseases and inflammatory conditions.
* **Cellular Growth and Differentiation:** Calcitriol plays a role in regulating cell growth and differentiation, influencing the development and function of various tissues, including bone, skin, and immune cells. This makes it relevant to research on cancer and other diseases related to cellular growth and differentiation.
* **Cardiovascular Health:** Calcitriol has been shown to influence blood pressure and vascular function. Research is ongoing to understand its potential role in preventing cardiovascular diseases.
* **Neurological Function:** Calcitriol has been linked to cognitive function, mood regulation, and the development of the nervous system. Further research explores its potential impact on neurological disorders and cognitive decline.

**Research Focus:**

1α,24-Dihydroxyvitamin D3 is an active area of research due to its diverse physiological functions and potential therapeutic applications. Some key research focuses include:

* **Understanding the mechanisms of action:** Researchers are exploring how calcitriol interacts with its receptors and signaling pathways to exert its various effects.
* **Therapeutic potential:** Studies are investigating the use of calcitriol and its analogs to treat conditions like osteoporosis, autoimmune diseases, cancer, and cardiovascular diseases.
* **Vitamin D deficiency:** Researchers are studying the role of vitamin D deficiency in various health issues and exploring ways to optimize vitamin D levels through supplementation and lifestyle modifications.

**In conclusion,** 1α,24-dihydroxyvitamin D3 is a vital molecule with diverse biological roles. Its research significance lies in its potential to shed light on various physiological processes and provide insights for developing new therapeutic strategies for treating various diseases.

1 alpha,24-dihydroxyvitamin D3: RN refers to (1alpha,3beta,5Z,7E)-isomer; formulated in ointment at a concentration of 4 microg/g, for treatment of mild psoriasis [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID90474059
MeSH IDM0081550

Synonyms (1)

Synonym
1 alpha,24-dihydroxyvitamin d3

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The treatment with a twice daily application of 2 micrograms/g ointment is efficacious and safe in Japanese patients."( Tacalcitol ointment in the treatment of psoriasis vulgaris: a multicentre, placebo-controlled, double-blind study on efficacy and safety.
Czarnetzki, BM; Haustein, UF; Luger, T; Niemann, R; Plänitz-Stenzel, V; Van de Kerkhof, PC; Werfel, T, 1996
)
0.29
" Treatment was generally well tolerated and there were no serious or unexpected adverse events reported."( Long-term efficacy and safety of tacalcitol ointment in patients with chronic plaque psoriasis.
Berth-Jones, J; Griffiths, CE; Harrison, PV; Hönigsmann, H; Marks, R; Roelandts, R; Schöpf, E; Trompke, C; van de Kerkhof, PC, 2002
)
0.31
"Tacalcitol ointment once daily was demonstrated to be efficacious, safe and well tolerated in the long-term control of plaque psoriasis in patients with up to 20% body surface involvement."( Long-term efficacy and safety of tacalcitol ointment in patients with chronic plaque psoriasis.
Berth-Jones, J; Griffiths, CE; Harrison, PV; Hönigsmann, H; Marks, R; Roelandts, R; Schöpf, E; Trompke, C; van de Kerkhof, PC, 2002
)
0.31
" Twenty-five local adverse drug reactions were noticed in 16 of the 154 subjects included in the safety analysis."( Long-term safety and efficacy of high-concentration (20 microg/g) tacalcitol ointment in psoriasis vulgaris.
Harada, S; Hori, Y; Miyachi, Y; Nakagawa, H; Nishiyama, S; Ohkawara, A; Ohkido, M; Tamaki, K,
)
0.13
" Our purpose is to compare the rates of adverse events associated with different topical psoriasis treatments."( A systematic review of adverse effects associated with topical treatments for psoriasis.
Bruner, CR; Feldman, SR; Fleischer, AB; Ventrapragada, M, 2003
)
0.32
"The results of this study indicate that topical application of tacalcitol (4 micro g/g) emulsion once daily is an effective, safe and very well- tolerated treatment for scalp psoriasis."( [Treatment of scalp psoriasis. An effective and safe tacalcitol emulsion].
Ruzicka, T; Trompke, C, 2004
)
0.32
"Many efforts have been made to obtain active and less toxic Vitamin D analogs for new clinical applications."( Toxicity and antineoplastic effect of (24R)-1,24-dihydroxyvitamin D3 (PRI-2191).
Dzimira, S; Kuśnierczyk, H; Kutner, A; Madej, J; Opolski, A; Pełczyńska, M; Szelejewski, W; Wietrzyk, J, 2004
)
0.32
"Active and less toxic vitamin D analogs could be useful for clinical applications."( Toxicity and antitumor activity of the vitamin D analogs PRI-1906 and PRI-1907 in combined treatment with cyclophosphamide in a mouse mammary cancer model.
Filip, B; Kutner, A; Milczarek, M; Nevozhay, D; Wietrzyk, J, 2008
)
0.35
"The LD50 values after five daily subcutaneous (s."( Toxicity and antitumor activity of the vitamin D analogs PRI-1906 and PRI-1907 in combined treatment with cyclophosphamide in a mouse mammary cancer model.
Filip, B; Kutner, A; Milczarek, M; Nevozhay, D; Wietrzyk, J, 2008
)
0.35

Compound-Compound Interactions

ExcerptReferenceRelevance
" Applying antiproliferative SRB and MTT assays, we measured the growth inhibitory effects of vitamin D compounds applied alone or in combination with either cisplatin or doxorubicin."( Correlation between VDR expression and antiproliferative activity of vitamin D3 compounds in combination with cytostatics.
Jaroszewicz, I; Kutner, A; Nevozhay, D; Opolski, A; Pelczynska, M; Switalska, M; Wietrzyk, J; Zabel, M,
)
0.13
" Applying antiproliferative SRB and MTT assays, the growth inhibitory effects of the vitamin D compounds, applied alone or in combination with either cisplatin or doxorubicin, were measured."( Antiproliferative activity of vitamin D compounds in combination with cytostatics.
Jaroszewicz, I; Kutner, A; Maciejewska, M; Opolski, A; Pelczynska, M; Switalska, M,
)
0.13
" The aim of this study was to investigate the possible influence of 1alpha,25-dihydroxyvitamin D(3) (calcitriol) and 1alpha,24(R)-dihydroxyvitamin D(3) (tacalcitol) in monotherapy and in combination with budesonid R (BR) on NP fibroblast proliferation."( Influence of vitamin D(3) analogues in combination with budesonid R on proliferation of nasal polyp fibroblasts.
Fraczek, M; Gawron, W; Latocha, M; Rostkowska-Nadolska, B, 2009
)
0.35
" The objective of this open label, intraindividual, left right study was to compare two different vitamin D analogues, calcipotriol and tacalcitol, in combination with NBUVB phototherapy in chronic stable plaque psoriasis."( Comparative evaluation of efficacy and safety of calcipotriol versus tacalcitol ointment, both in combination with NBUVB phototherapy in the treatment of stable plaque psoriasis.
Aggarwal, K; Dua, I; Jain, VK, 2017
)
0.46
" Vitamin D compounds have been shown to exert synergistic effects when used in combination with different agents used in anticancer therapies in different cancer models."( Vitamin D derivatives potentiate the anticancer and anti-angiogenic activity of tyrosine kinase inhibitors in combination with cytostatic drugs in an A549 non-small cell lung cancer model.
Filip-Psurska, B; Kutner, A; Maj, E; Milczarek, M; Psurski, M; Wietrzyk, J, 2018
)
0.48

Dosage Studied

ExcerptRelevanceReference
" The rats were dosed orally with each sterol for 7 days at a rate of 1 ng/g body weight/day."( Comparison of the relative effects of 1,24-dihydroxyvitamin D(2) [1, 24-(OH)(2)D(2)], 1,24-dihydroxyvitamin D(3) [1,24-(OH)(2)D(3)], and 1,25-dihydroxyvitamin D(3) [1,25-(OH)(2)D(3)] on selected vitamin D-regulated events in the rat.
Bishop, C; Horst, R; Knutson, J; Koszewski, N; Prapong, S; Reinhardt, T, 2000
)
0.31
" The mean number of sessions and the cumulative dosage for initial repigmentation were calculated."( Topical tacalcitol and 308-nm monochromatic excimer light: a synergistic combination for the treatment of vitiligo.
Lei-hong, X; Lu-yan, T; Wen-wen, F; Yi, J; Zhi-zhong, Z, 2006
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (182)

TimeframeStudies, This Drug (%)All Drugs %
pre-199023 (12.64)18.7374
1990's43 (23.63)18.2507
2000's62 (34.07)29.6817
2010's49 (26.92)24.3611
2020's5 (2.75)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 9.17

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index9.17 (24.57)
Research Supply Index5.51 (2.92)
Research Growth Index4.68 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (9.17)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials39 (18.84%)5.53%
Reviews15 (7.25%)6.00%
Case Studies37 (17.87%)4.05%
Observational0 (0.00%)0.25%
Other116 (56.04%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase 3 Study Comparing a Gel Containing Calcipotriol 50 mcg/g Plus Betamethasone 0.5 mg/g (as Dipropionate) With Tacalcitol Ointment (4 mcg/g) and Gel Vehicle, Used Once Daily in the Treatment of Psoriasis Vulgaris [NCT00670241]Phase 3458 participants (Actual)Interventional2008-04-30Completed
A Phase 3 Study Comparing an Ointment Containing Calcipotriol 25 mcg/g Plus Hydrocortisone 10 mg g With Tacalcitol 4 mcg/g Ointment and the Ointment Vehicle Alone, All Applied Once Daily in the Treatment of Psoriasis Vulgaris on the Face and on the Intert [NCT00640822]Phase 3782 participants (Actual)Interventional2008-02-29Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00640822 (1) [back to overview]Subjects With Controlled Disease According to the Investigator Assessment of the Face at Week 8
NCT00670241 (5) [back to overview]"Subjects With Controlled Disease (Clear or Almost Clear Disease) According to Investigator's Global Assessment of Disease Severity at Week 8"
NCT00670241 (5) [back to overview]"Subjects With Controlled Disease According to the Investigator's Global Assessment of Disease Severity at Week 4"
NCT00670241 (5) [back to overview]Subjects With Rebound During the Study
NCT00670241 (5) [back to overview]Subjects With Relapse During the Study
NCT00670241 (5) [back to overview]The Percentage Change in PASI From Baseline to Week 8

Subjects With Controlled Disease According to the Investigator Assessment of the Face at Week 8

(NCT00640822)
Timeframe: Week 8

InterventionParticipants (Number)
Calcipotriol Plus Hydrocortisone Ointment183
Tacalcitol Ointment147
Calcipotriol Plus Hydrocortisone Ointment Vehicle37

[back to top]

"Subjects With Controlled Disease (Clear or Almost Clear Disease) According to Investigator's Global Assessment of Disease Severity at Week 8"

(NCT00670241)
Timeframe: Week 8

InterventionParticipants (Number)
Calcipotriol Plus Betamethasone Dipropionate Gel73
Tacalcitol Ointment33
Gel Vehicle5

[back to top]

"Subjects With Controlled Disease According to the Investigator's Global Assessment of Disease Severity at Week 4"

(NCT00670241)
Timeframe: Week 4

Interventionparticipants (Number)
Calcipotriol Plus Betamethasone Dipropionate Gel34
Tacalcitol Ointment12
Gel Vehicle1

[back to top]

Subjects With Rebound During the Study

(NCT00670241)
Timeframe: Week 8-16

Interventionparticipants (Number)
Calcipotriol Plus Betamethasone Dipropionate Gel0
Tacalcitol Ointment0
Gel Vehicle0

[back to top]

Subjects With Relapse During the Study

Among subjects with controlled disease at week 8 relapse was defined as PASI exceeding the baseline PASI value minus 50% of the reduction in PASI obtained from the baseline visit to the last on-treatment visit (NCT00670241)
Timeframe: Week 8-16

Interventionparticipants (Number)
Calcipotriol Plus Betamethasone Dipropionate Gel28
Tacalcitol Ointment7
Gel Vehicle3

[back to top]

The Percentage Change in PASI From Baseline to Week 8

PASI is Psoriasis Area and Severity Index and is based on the investigator's assessment of extent and severity of the disease. It can range from 0 (best) to 64.8 (worst). (NCT00670241)
Timeframe: Baseline, Week 4 and 8

InterventionPercent change in PASI score (Number)
Calcipotriol Plus Betamethasone Dipropionate Gel-57.0
Tacalcitol Ointment-41.9
Gel Vehicle-17.9

[back to top]