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Mots-C

Mitochondrial open reading frame of the 12S rRNA-c, MT-RNR1, Mitochondrial-derived peptide MOTS-c

Quick Stats
Studies 137
Trials 5
Score 2
2021 pubmed 15 citations

Relationship between the mitochondria-derived peptide MOTS-c and insulin resistance in obstructive sleep apnea.

Baylan. Filiz Alkan FA; Yarar. Esra E

Key Findings

  • MOTS‑c levels are significantly lower in people with obstructive sleep apnea compared to healthy controls
  • MOTS‑c levels drop further as sleep apnea severity and BMI increase
  • Lower MOTS‑c is independently associated with higher apnea‑hypopnea index and insulin resistance (HOMA‑IR)

Practical Outcomes

  • For biohackers, MOTS‑c could serve as a potential blood marker to flag early metabolic issues in sleep‑disordered breathing. While the study doesn’t test any interventions, it suggests that strategies aimed at raising MOTS‑c (e.g., exercise, certain diets) might help improve insulin sensitivity, especially in those with sleep apnea.

Summary

Researchers measured a tiny protein called MOTS‑c in people with sleep apnea and found that lower levels are linked to worse breathing problems, higher body weight, and more insulin resistance, which are all risk factors for metabolic disease.

Abstract

The co-occurrence of obstructive sleep apnea (OSA) and obesity are common. Mitochondrial open reading frame of the 12S rRNA-c (MOTS-C) is one of the newly identified mitochondrial derivative peptides that play a role in the regulation of metabolic homeostasis. We aimed to examine the serum levels of MOTS-C to help understand the role of the disease in the pathophysiology, thereby investigating whether it can contribute to the appropriate treatment. Seventy patients with OSAS and 20 healthy controls were included. The serum MOTS-C level was measured in all patients. For each participant, demographic features, lipid profile, serum glucose levels, and insulin levels were also evaluated. Homeostatic model assessment indicator of insulin resistance (HOMA-IR) was calculated for all participants. Patients with OSAS (n = 70) were grouped as mild (n = 19), moderate (n = 19), and severe (n = 32). Patients with AHI ≤ 5 were considered as the healthy control group (n = 20). Mean age was 50.3 years and 74% (67/90) of the study sample was male. As expected, as the severity of OSA increased, BMI, insulin levels and HOMA-IR increased. MOTS-C levels were significantly lower in patients with OSA compared to healthy controls (p < 0.000) and we found that MOTS-C levels decreased as OSA severity increased. There was a negative correlation between serum MOTS-C levels and AHI and BMI (r = - 0.492, p < 0.001, r = - 0.382, p < 0.001, respectively). Serum MOTS-C levels were independently associated with AHI in BMI and HOMA-IR in linear regression analysis (p < 0.010, p < 0.007, p < 0.007, respectively). Serum MOTS-C level is related to OSA and BMI. MOTS-C may be a useful new marker for early metabolic disorders in patients with OSA.

Study Information

Provider

pubmed

Year

2021

Date

2021-01-04T00:00:00.000Z

DOI

10.1007/s11325-020-02273-0

Citations

15

References

37