Evaluation of serum samples in long cryopreservation for SomaScan proteomics and sex differences in elderly Japanese adults

Many biobanks store biological samples and use them for various analyses, including proteomics. Therefore, it is necessary to consider the denaturation of target proteins during long-term storage. We analyzed 16-year-old cryopreserved serum samples using the SomaScan platform, a novel proteomic assay, to determine whether adiponectin and resistin concentrations were consistent with those measured in our previous studies using a different platform. The results suggested that long-term cryopreserved serum samples could be used for future studies of at least adiponectin and resistin, which are closely related to the pathophysiology of diabetes, cardiovascular disease, and other metabolic diseases. Therefore, 7,289 SomaScan-assayed circulating proteins were compared between 20 men and 20 women aged ≥ 50 to determine sex differences. In total, 20 serum proteins showed significant sex differences. Of these, proteins that showed a more than two-fold difference in concentration between sexes contained heterodimeric forms of gonadotropic proteins such as CGA|FSHB, CGA|CGB3|CGB7, and CGA|LHB, which are the biologically active forms of these hormones. The present study is the first to report the possibility of using long-term cryopreserved serum samples for the SomaScan assay, and the results show that the SomaScan assay may be useful for analyzing sex differences focusing on gonadotropic hormones.

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Journal
Scientific Reports
Published
2025-08-14
DOI
https://doi.org/10.1038/s41598-025-14464-4
Citations
1
Primary Topic
Adipokines, Inflammation, and Metabolic Diseases
Type
article
Field-Weighted Citation Impact
1.35

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article

Evaluation of serum samples in long cryopreservation for SomaScan proteomics and sex differences in elderly Japanese adults

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1 citations
Scientific Reports
Adipokines, Inflammation, and Metabolic Diseases
1.35
article

Evaluation of serum samples in long cryopreservation for SomaScan proteomics and sex differences in elderly Japanese adults

Tomoko S. Kato, Yuki Ohashi, Masahisa Katsuno, Masahiro Nakatochi, Tatsuaki Matsubara, Sahoko Ichihara, Fumie Kinoshita, Ken Yamamoto, Mitsuhiro Yokota, Ruriha Beppo
article en
1 citations

Abstract

Many biobanks store biological samples and use them for various analyses, including proteomics. Therefore, it is necessary to consider the denaturation of target proteins during long-term storage. We analyzed 16-year-old cryopreserved serum samples using the SomaScan platform, a novel proteomic assay, to determine whether adiponectin and resistin concentrations were consistent with those measured in our previous studies using a different platform. The results suggested that long-term cryopreserved serum samples could be used for future studies of at least adiponectin and resistin, which are closely related to the pathophysiology of diabetes, cardiovascular disease, and other metabolic diseases. Therefore, 7,289 SomaScan-assayed circulating proteins were compared between 20 men and 20 women aged ≥ 50 to determine sex differences. In total, 20 serum proteins showed significant sex differences. Of these, proteins that showed a more than two-fold difference in concentration between sexes contained heterodimeric forms of gonadotropic proteins such as CGA|FSHB, CGA|CGB3|CGB7, and CGA|LHB, which are the biologically active forms of these hormones. The present study is the first to report the possibility of using long-term cryopreserved serum samples for the SomaScan assay, and the results show that the SomaScan assay may be useful for analyzing sex differences focusing on gonadotropic hormones.

Scientific ReportsVol. 15(1)
Kurume University (JP), Nagoya University Hospital (JP), Kurume University Medical Center (JP), Aichi Mizuho College (JP), Nagoya University (JP)
Suzuken Memorial Foundation, Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science
Good health and well-being
Openalex Percentile: Top 17%
Adipokines, Inflammation, and Metabolic Diseases
1.35
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