Preview

Neurology, Neuropsychiatry, Psychosomatics

Advanced search

Curcumin as add-on therapy in patients with multiple sclerosis showing a suboptimal response to first-line disease-modifying therapies: clinical outcomes and in vitro data

https://doi.org/10.14412/20742711-2025-3-11-18

Abstract

In recent decades, pathogenetic therapy of multiple sclerosis (MS) has advanced significantly due to the development of disease-modifying therapies (DMTs), which are classified into first- and second-line drugs based on their efficacy and safety profiles. Curcumin is being considered as an add-on therapy due to its potential efficacy and favorable safety profile.

Objective: to evaluate the effect of micellar curcumin on clinical and immunological parameters in MS patients receiving interferon (IFN) therapy, as well as to assess the in vitro effects of this polyphenol on cytokine production by macrophages (MFs) and peripheral blood mononuclear cells (PBMCs).

Material and methods. As a result of randomization, MS patients (n=60) with a suboptimal response to IFNβtherapy were divided into two groups, one of which received additional therapy with micellar curcumin for 6 months (IFN-C group). Clinical (relapses, MRI activity, EDSS score, chronic fatigue according MFIS scale, quality of life according SF-36) and immunological (IL-6 and IFNγ levels) parameters were assessed before and after the study. The effect of curcumin on cytokine production by PBMCs and MFs in MS patients and healthy donors was also evaluated.

Results. After 6 months, the IFN-C group showed a decrease in the proportion of patients with relapses (p=0.007), a reduction in the proportion of patients with new/enlarging lesions on T2 MRI (p=0.003), and stabilization of EDSS score (p=0.2), in contrast to the comparison group, which showed increased disability (p=0.03). Hazard ratio for exacerbation in the curcumin group compared to the control group was 0.2 (95% CI 0.09–0.89; p=0.03). This group also showed improvement in chronic fatigue (p=0.002) and quality of life (p=0.008 for physical and p=0.03 for mental components). No adverse events were reported during the observation period. After dietary enrichment, a lower level of IFNγwas detected in the plasma of patients receiving curcumin (p=0.02). In vitro results demonstrated a slight stimulatory effect of curcumin on IL-10 and an inhibitory effect on IL-6 and IFNγ.

Conclusion. Based on the results of this pilot study, micellar forms of curcumin, that have an acceptable safety profile, may be considered as a potential adjunctive method to enhance the anti-inflammatory effect of IFNβin MS patients with suboptimal therapeutic response.

About the Authors

A. D. Kukushkina
Department of Neurology, Neurosurgery and Medical Genetics, N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia; Department of Neuroimmunology, Federal Center for Brain and Neurotechnologies, FMBA of Russia; Zhadkevich Moscow City Clinical Hospital
Russian Federation

Anna Dmitrievna Kukushkina

1, Ostrovityanovа St., Moscow 117997

1, Ostrovityanovа St., Build. 10, Moscow 117997

14, Mozhaiskoe Sh., Moscow 121374


Competing Interests:

There are no conflicts of interest



V. S. Rogovskii
Department of Molecular Pharmacology and Radiobiology named after P.V. Sergeev, N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia; Department of Neuroimmunology, Federal Center for Brain and Neurotechnologies, FMBA of Russia
Russian Federation

1, Ostrovityanovа St., Moscow 117997

1, Ostrovityanovа St., Build. 10, Moscow 117997


Competing Interests:

There are no conflicts of interest



E. V. Ponevezhskaia
Zhadkevich Moscow City Clinical Hospital
Russian Federation

14, Mozhaiskoe Sh., Moscow 121374


Competing Interests:

There are no conflicts of interest



E. V. Lysogorskaia
Zhadkevich Moscow City Clinical Hospital
Russian Federation

14, Mozhaiskoe Sh., Moscow 121374


Competing Interests:

There are no conflicts of interest



A. N. Boyko
Department of Neurology, Neurosurgery and Medical Genetics, N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia; Department of Neuroimmunology, Federal Center for Brain and Neurotechnologies, FMBA of Russia
Russian Federation

1, Ostrovityanovа St., Moscow 117997

1, Ostrovityanovа St., Build. 10, Moscow 117997


Competing Interests:

There are no conflicts of interest



References

1. Clinical management of multiple sclerosis around the world. Key findings about the diagnosis and clinical management of MS Atlas of MS. 3rd ed. 2021.

2. Rafiee Zadeh A, Ghadimi K, Ataei A, et al. Mechanism and adverse effects of multiple sclerosis drugs: a review article. Part 2. Int J Physiol Pathophysiol Pharmacol. 2019 Aug 15;11(4):105-14.

3. Ghoushi E, Poudineh M, Parsamanesh N, et al. Curcumin as a regulator of Th17 cells: Unveiling the mechanisms. Food Chem (Oxf). 2024 Mar 12;8:100198. doi: 10.1016/j.fochms.2024.100198

4. Amiri Z, Jalili S, Tarahomi M, et al. Curcumin's spice-infused therapeutic promise: disease severity alleviation in a mouse model of multiple sclerosis via modulation of immune responses. Mol Biol Rep. 2023 Nov;50(11):8843- 53. doi: 10.1007/s11033-023-08781-y. Epub 2023 Sep 3.

5. Роговский ВС, Кукушкина АД, Бойко АН. Перспективы применения куркумина в комплексной терапии рассеянного склероза. Неврология, нейропсихиатрия, психосоматика. 2023;15(Прил. 1):65-70. doi: 10.14412/2074-2711-2023-1S-65-70

6. Kocher A, Bohnert L, Schiborr C, Frank J. Highly bioavailable micellar curcuminoids accumulate in blood, are safe and do not reduce blood lipids and inflammation markers in moderately hyperlipidemic individuals. Mol Nutr Food Res. 2016 Jul;60(7):1555-63. doi: 10.1002/mnfr.201501034. Epub 2016 May 23.

7. Grafeneder J, Derhaschnig U, Eskandary F, et al. Micellar Curcumin: Pharmacokinetics and Effects on Inflammation Markers and PCSK-9 Concentrations in Healthy Subjects in a Double-Blind, Randomized, Active-Controlled, Crossover Trial. Mol Nutr Food Res. 2022 Nov;66(22):e2200139. doi: 10.1002/mnfr.202200139. Epub 2022 Sep 13.

8. Schiborr C, Kocher A, Behnam D, et al. The oral bioavailability of curcumin from micronized powder and liquid micelles is significantly increased in healthy humans and differs between sexes. Mol Nutr Food Res. 2014 Mar;58(3):516-27. doi: 10.1002/mnfr.201300724. Epub 2014 Jan 9. Erratum in: Mol Nutr Food Res. 2014 Mar;58(3):647. Dosage error in article text.

9. Lazzarotto Braga T, Dias Pereira CI, Ricken Y, et al. Behavior of Curcumin in micellar biomimetic systems and its protolytic and tautomeric equilibria elucidated by multivariate analysis. J Mol Liq Elsevier. 2024;394:123729.

10. Petracca M, Quarantelli M, Moccia M, et al. ProspeCtive study to evaluate efficacy, safety and tOlerability of dietary supplemeNT of Curcumin (BCM95) in subjects with Active relapsing MultIple Sclerosis treated with subcutaNeous Interferon beta 1a 44 mcg TIW (CONTAIN): A randomized, controlled trial. Mult Scler Relat Disord. 2021 Nov;56:103274. doi: 10.1016/j.msard.2021.103274

11. Dolati S, Ahmadi M, Aghebti-Maleki L, et al. Nanocurcumin is a potential novel therapy for multiple sclerosis by influencing inflammatory mediators. Pharmacol Rep. 2018 Dec;70(6):1158-67. doi: 10.1016/j.pharep.2018.05.008

12. Dolati S, Ahmadi M, Rikhtegar R, et al.Changes in Th17 cells function after nanocurcumin use to treat multiple sclerosis. Int Immunopharmacol. 2018 Aug;61:74-81. doi: 10.1016/j.intimp.2018.05.018

13. Dolati S, Babaloo Z, Ayromlou H, et al.Nanocurcumin improves regulatory T-cell fre quency and function in patients with multiple sclerosis. J Neuroimmunol. 2019 Feb 15;327:15 21. doi: 10.1016/j.jneuroim.2019.01.007

14. Кукушкина АД, Роговский ВС, Поневежская ЕВ и др. Куркумин в качестве добавочной терапии рассеянного склероза у пациентов, получающих терапию интерферонами бета. Неврология, нейропсихиатрия, психосоматика. 2024;16(Прил. 2):4-10. doi: 10.14412/20742711-2024-2S-4-10

15. Peng Y, Ao M, Dong B, et al. Anti-Inflammatory Effects of Curcumin in the Inflammatory Diseases: Status, Limitations and Countermeasures. Drug Des Devel Ther. 2021 Nov 2;15:4503-25. doi: 10.2147/DDDT.S327378

16. Zhao G, Liu Y, Yi X, et al. Curcumininhibiting Th17 cell differentiation by regulating the metabotropic glutamate receptor-4 expression on dendritic cells. Int Immunopharmacol. 2017 May;46:80-6. doi: 10.1016/j.intimp.2017.02.017

17. Xu J, Yuan C, Wang G, et al. UrolithinsAttenuate LPS-Induced Neuroinflammation in BV2Microglia via MAPK, Akt, and NF-κB Signaling Pathways. J Agric Food Chem. 2018 Jan 24;66(3):571-80. doi: 10.1021/acs.jafc.7b03285. Epub 2018 Jan 16.

18. Zheng XF, Hong YX, Feng GJ, et al.Lipopolysaccharide-induced M2 to M1 macrophage transformation for IL-12p70 production is blocked by Candida albicans mediated up-regulation of EBI3 expression. PLoS One. 2013 May 27;8(5):e63967. doi: 10.1371/journal.pone.0063967


Review

For citations:


Kukushkina AD, Rogovskii VS, Ponevezhskaia EV, Lysogorskaia EV, Boyko AN. Curcumin as add-on therapy in patients with multiple sclerosis showing a suboptimal response to first-line disease-modifying therapies: clinical outcomes and in vitro data. Nevrologiya, neiropsikhiatriya, psikhosomatika = Neurology, Neuropsychiatry, Psychosomatics. 2025;17(3):11–18. (In Russ.) https://doi.org/10.14412/20742711-2025-3-11-18

Views: 161


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2074-2711 (Print)
ISSN 2310-1342 (Online)