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Total caffeine intake is associated with lower serum α-Klotho and may impact its detection accuracy: Evidence from NHANES 2007 to 2016 and molecular docking.

総カフェイン摂取は血清α-クロトー低下と関連し、その検出精度に影響を与える可能性がある:NHANES 2007〜2016と分子ドッキングからのエビデンス (機械翻訳の邦題)

Medicine2025Shi FE, Yu Z, Huang Z, et al.
研究デザインその他の原著論文
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記録の確認項目

研究デザイン
その他の原著論文
対象
ヒト
出版年
2025
出典
doi.org
抄録の表示
表示あり
出版状態
有効な記録
状態確認日
2026/08/17
収集日
2026/08/03
鮮度
確認期限内
確認段階
自動処理
記録状態
公開

日本語要約(機械生成)

本研究は、総カフェイン摂取(TCI)と老化関連バイオマーカーである血清α-クロトー(KL)の関連を検討した横断研究である。NHANES 2007〜2016の40〜79歳の成人データを用い、一般化線形回帰、制限付き三次スプライン、サブグループ解析、分子ドッキングを実施した。その結果、TCIが高いほど血清KLレベルが有意に低く、完全調整モデルでは最低群と比較して第3群で-30.21 pg/mL、第4群で-27.31 pg/mLの低下が認められ、線形の用量反応関係が示された。負の関連は60歳未満、過体重/肥満、女性で顕著であった。分子ドッキングではカフェインとKLの直接相互作用が示唆され、結合エネルギーは-5.299 kcal/molで安定した結合を示した。これらの結果はカフェインの老化促進効果の可能性を示唆し、またカフェインがKLの免疫測定に干渉する可能性があるため、検査前のカフェイン摂取回避がバイオマーカー精度向上に重要であると結論付けた。

この要約は公開抄録のみを根拠にAIが機械的に生成したものです。正確な内容は原文を確認してください。

抄録

The relationship between total caffeine intake (TCI) and aging remains understudied. α-Klotho (KL), a key aging-related circulating biomarker, is clinically valuable. Unlike prior studies focusing on coffee intake, we analyzed TCI (from diet and supplements) to isolate its independent association with KL and explore mechanisms via molecular docking. We thus conducted a cross-sectional analysis with NHANES 2007 to 2016 data to investigate TCI and serum KL levels in adults aged 40 to 79. Serum KL levels were determined using ELISA kits, while trained interviewers assessed TCI through 24-hour dietary recalls. Generalized linear regression models were employed to evaluate the correlation between TCI and serum KL levels. We utilized restricted cubic spline analysis to explore the dose-response relationship between the 2 factors. Subgroup analyses and molecular docking studies were also conducted to further understand the association. After adjusting for potential confounders, higher TCI was significantly associated with lower serum KL levels. In the fully adjusted model, compared to the lowest TCI group, KL levels decreased by -30.21 pg/mL (95% CI = -50.49 to -9.93 pg/mL) and -27.31 pg/mL (95% CI = -51.94 to -2.67 pg/mL) in the third and fourth groups, respectively, indicating a significant trend (P for trend = .005). Restricted cubic spline analysis revealed a linear dose-response relationship (P for nonlinearity = .362). Subgroup analyses showed that the negative correlation was more pronounced in participants aged < 60 years, those who were overweight/obese, and females. Molecular docking analysis suggested a direct interaction between caffeine and KL, with a binding energy of -5.299 kcal/mol, implying a stable interaction. These results suggest a potential pro-aging effect of caffeine. Further prospective studies and experimental validation are needed to clarify caffeine's effects on KL. Notably, molecular docking indicates caffeine may interfere with α-Klotho immunoassay detection, emphasizing the need for caffeine abstinence before testing to enhance biomarker accuracy.

MeSH

AdultAgedBiomarkersCaffeineCross-Sectional StudiesFemaleGlucuronidaseHumansKlotho ProteinsMaleMiddle AgedMolecular Docking SimulationNutrition Surveys

DOI 10.1097/md.0000000000046592

PMID 41465998

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