Fact checked byKristen Dowd

Read more

August 14, 2023
2 min read
Save

Lower vitamin K levels linked to poor lung function, greater COPD, asthma risks

Fact checked byKristen Dowd
You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

Key takeaways:

  • Low vitamin K levels appeared linked to decreased measures of FEV1 and FVC following adjustments for several variables.
  • The risk for self-reported COPD, wheezing and asthma was heightened with lower vitamin K.

Lower vitamin K levels appeared associated with declines in lung function measures and greater risk for self-reported COPD, asthma and wheezing, according to study results published in ERJ Open Research.

Torkil Jespersen

“[This study] shows a need for more extensive studies on whether lung patient groups and the general population may benefit from taking vitamin K supplements,” Torkil Jespersen, MD, master’s thesis student in the Center for Clinical Research and Prevention at Frederiksberg Hospital in Denmark, told Healio.

Infographic showing risk for self-reported lung diseases/symptoms with low vitamin K levels (doubled dp-ucMGP plasma) in fully adjusted model.
Data were derived from Jespersen T, et al. ERJ Open Res. 2023;doi:10.1183/23120541.00208-2023.

In a cross-sectional population-based study, Jespersen and colleagues analyzed 4,092 adults (age range, 24 to 77 years) from the Danish study of Functional Disorders general population cohort to determine how vitamin K levels are related to lung function and lung diseases using regression models adjusted for age, sex and height.

Researchers collected spirometry and dephosphorylated-uncarboxylated Matrix Gla protein (dp-ucMGP) plasma levels — higher levels of which suggested lower vitamin K levels — and had the participants complete questionnaires.

Reduced measures of FEV1 and FVC appeared related to low vitamin K levels/increased dp-ucMGP (FEV1 per doubling of dp-ucMGP = –97.8 mL; 95% CI, –141.3 mL to –54.4 mL; FVC per doubling of dp-ucMGP = –136 mL; 95% CI, –187.2 mL to –84.9 mL) in the model adjusted for age, sex and height.

Researchers continued to observe declines in these measures with the doubling of dp-ucMGP following further adjustment for weight and kidney function (FEV1 = –72.8 mL; 95% CI, –117.5 mL to –28.2 mL; FVC = –84.2 mL; 95% CI, –136.3 mL to –32.2 mL) and for smoking, alcohol consumption, physical activity, fitness and healthy eating (FEV1 = –50.3 mL; 95% CI, –95 mL to –5.5 mL; FVC = –54.8 mL; 95% CI, –107.4 mL to –2.1 mL).

Additionally, doubling of dp-ucMGP increased the risk for FEV1 and FVC below lower limit of normal (FEV1, adjusted OR = 2.41; 95% CI, 1.65-3.52; FVC, aOR = 2.48; 95% CI, 1.46-4.22) in the model adjusted for age, sex and height, although researchers noted this association lessened with further adjustments.

Researchers did not find a link between vitamin K and FEV1/FVC ratio.

“We were surprised to find vitamin K status was not associated with lower FEV1/FVC ratio, which one would expect to see in obstructive lung diseases such as asthma and COPD,” Jespersen told Healio.

Lastly, researchers observed heightened odds for self-reported lung diseases/symptoms in the fully adjusted model when individuals had low vitamin K levels/doubled dp-ucMGP plasma, with the greatest risk found for COPD (aOR = 2.09; 95% CI, 1.35-3.23), followed by wheezing (aOR = 1.4; 95% CI, 1.08-1.81) and asthma (aOR = 1.29; 95% CI, 0.99-1.67).

“Future studies will be prospective, meaning they will follow vitamin K status and lung function in individuals over time,” Jespersen told Healio. “Further, several authors of the article are currently involved in a long-term randomized placebo-controlled trial (InterVitaminK) to see whether vitamin K supplementation influences age-related diseases including chronic lung disease.”

Reference:

For more information:

Torkil Jespersen, MD, can be reached at torkil.jespersen.02@regionh.dk.