Evidence map›Paper›PMID 41852407›Full record

ArticleFrontiers in microbiomes2025

Microbial dysbiosis in melasma through community profiling.

Yugandhar Reddy B S, Chandraprabha Doraiswamy, Deepshikha Singh, Nagalakshmi Surendra, Aparna Damle, Maitreyee Dutta, Savitha Rajkumar, Brian Potterf, Arindam Roy, Bharat Cheviti and 7 more

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Article in Frontiers in microbiomes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Yugandhar Reddy B SUnilever Research & Development, Bangalore, India.
Chandraprabha DoraiswamyUnilever Research & Development, Bangalore, India.
Deepshikha SinghDepartment of Biochemistry, Indian Institute of Science, Bangalore, India.
Nagalakshmi SurendraUnilever Research & Development, Bangalore, India.
Aparna DamleUnilever Research & Development, Bangalore, India.
Maitreyee DuttaUnilever Research & Development, Bangalore, India.
Savitha RajkumarUnilever Research & Development, Bangalore, India.
Brian PotterfUnilever Research & Development, Trumbull, CT, United States.
Arindam RoyUnilever Research & Development, Bangalore, India.
Bharat ChevitiUnilever Research & Development, Bangalore, India.
Tony DaddUnilever Research & Development, Colworth Science Park, Bedford, United Kingdom.
David ArnoldUnilever Research & Development, Port Sunlight Research Lab, Birkenhead, United Kingdom.
Sarah PatersonUnilever Research & Development, Port Sunlight Research Lab, Birkenhead, United Kingdom.
Mukta SachdevMS Clinical Research, Bangalore, India.
Paul Van-Der LogtUnilever Research & Development, Wageningen, Netherlands.
Nirmala NairUnilever Research & Development, Bangalore, India.
Nagasuma ChandraDepartment of Biochemistry, Indian Institute of Science, Bangalore, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The complex ecosystem on skin comprising tens of thousands of microorganisms plays an important role in health and disease. The last decade in particular has witnessed a surge in microbiome research, which has been elucidating the role of the microbiota in numerous skin pathologies. Of relevance to the current study, are recent evidences implicating the microbiome in skin pigmentary conditions. Melasma is one such refractory, hyperpigmentary condition with a poorly understood pathogenesis. The present study was carried out to characterize the nature of microbial dysbiosis and its impact on microbial community structure in melasma subjects. Results: The clinical assessment of melasma carried out using biophysical, biochemical and biomarker-based measures confirmed significant changes in melasma lesions, most notably, those linked to redox, inflammation and barrier properties. A deep characterization of the skin microbiome in melasma from human face, indicated significant differences between lesional and peri-lesional areas. Of the 377 genera identified through an agglomeration of all OTUs at the Genus level through 16S rRNA sequencing, 344 were common, while 12 were unique to lesional and 21 unique in peri-lesional areas. A significant decrease was observed in alpha diversity in melasma lesion as compared to peri-lesion areas, with an accompanying decrease in number of interconnections among them. The differences in the microbiome also appeared to correlate with several clinical parameters, notably with the melasma severity measured through modified MASI (mMASI) scoring. The observed changes in both host and microbiome, point to a potential role for the latter in melasma pathogenesis. Conclusions: Our study indicates that there are significant differences in the microbiome between lesional and peri-lesional areas of melasma subjects, with associated changes in microbial community structures. Additionally, the observed changes were seen to correlate with measured clinical parameters. These findings provide the opportunity to further probe the nature of host and microbiome links that may underlie the phenotypic manifestation, as well as provide effective routes for managing this recalcitrant disorder.

Indexed as

clinical analysiscommunity network analysismelasmamicrobial dysbiosisskin microbiome

Identifiers

PMID41852407
PMCPMC12993618

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.