Skip to main content

Effect of plasma polyunsaturated fatty acid levels on leukocyte telomere lengths in the Singaporean Chinese population

Abstract

Background

Shorter telomere length (TL) has been associated with poor health behaviors, increased risks of chronic diseases and early mortality. Excessive shortening of telomere is a marker of accelerated aging and can be influenced by oxidative stress and nutritional deficiency. Plasma n6:n3 polyunsaturated fatty acid (PUFA) ratio may impact cell aging. Increased dietary intake of marine n-3 PUFA is associated with reduced telomere attrition. However, the effect of plasma PUFA on leukocyte telomere length (LTL) and its interaction with genetic variants are not well established.

Methods

A nested coronary artery disease (CAD) case-control study comprising 711 cases and 638 controls was conducted within the Singapore Chinese Health Study (SCHS). Samples genotyped with the Illumina ZhongHua-8 array. Plasma n-3 and n-6 PUFA were quantified using mass spectrometry (MS). LTL was measured with quantitative PCR method. Linear regression was used to test the association between PUFA and LTL. The interaction between plasma PUFAs and genetic variants was assessed by introducing an additional term (PUFA×genetic variant) in the regression model. Analysis was carried out in cases and controls separately and subsequently meta-analyzed using the inverse-variance weighted method. We further assessed the association of PUFA and LTL with CAD risk by Cox Proportional-Hazards model and whether the effect of PUFA on CAD was mediated through LTL by using structural equation modeling.

Results

Higher n6:n3 ratio was significantly associated with shorter LTL (p = 0.018) and increased CAD risk (p = 0.005). These associations were mainly driven by elevated plasma total n-3 PUFAs, especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) (p < 0.05). There was a statistically significant interaction for an intergenic single nucleotide polymorphism (SNP) rs529143 with plasma total n-3 PUFA and DHA on LTL beyond the genome-wide threshold (p < 5 ×  10− 8). Mediation analysis showed that PUFA and LTL affected CAD risk independently.

Conclusions

Higher plasma n6:n3 PUFA ratio, and lower EPA and DHA n-3 PUFAs were associated with shorter LTL and increased CAD risk in this Chinese population. Furthermore, genetic variants may modify the effect of PUFAs on LTL. PUFA and LTL had independent effect on CAD risk in our study population.

Peer Review reports

Introduction

Telomeres are complexes at the ends of eukaryotic chromosomes, which consist of tandem repeat DNA sequences (TTAGGG)n for humans, and associated proteins [1]. Telomeres protects the genome from degradation, interchromosomal fusion, unnecessary recombination and being recognized as a double-strand break by DNA repair proteins [2]. Telomeres shorten progressively during cell divisions and eventually result in cellular senescence or apoptosis when telomere length (TL) reaches a critical limit [3]. Growing epidemiologic and clinical studies have shown that TL is associated with chronic diseases, including cancer [4], osteoporosis [5], and cardiovascular diseases [6]. These observations have led to telomeres being proposed as an important marker of biological age, which is independent of chronological age [7], and as a prognostic marker of chronic disease risk, progression and premature mortality [8, 9].

Dietary intake is a significant contributor in determining cellular TL. Intakes of both omega 3 (n-3) and omega-6 (n-6) polyunsaturated fatty acids (PUFAs) can influence inflammation [10], which may affect telomeres attrition rate both in vitro [11] and in vivo [12]. Higher n-3 PUFA concentration in plasma may have an anti-inflammatory effect [13], while n-6 PUFA shows pro-inflammatory and pro-thrombotic potential through synthesis of oxidized metabolites [14, 15]. There is competition between n-3 and n-6 PUFA for desaturation and elongation enzymes. The ratio of plasma n-6 and n-3 PUFA (n6:n3 ratio), may hence contribute to inflammatory profiles and health status of an individual [16].

Genetic studies have identified several loci associated with leukocyte telomere length (LTL) [17, 18]. However, the contribution of these variants, even in combination, to the overall heritability of LTL is modest. Interaction between genes and life-style factors may also contribute to LTL heritability. The aims of this study were to investigate the association between plasma PUFA levels and LTL in the Chinese population and to evaluate genetic variants that may modify this effect.

Method

Study population

The Singapore Chinese Health Study (SCHS) is a long-term population-based prospective cohort study focused on dietary, genetic and environmental determinants of cancer and other chronic diseases in Singapore [19]. From April 1993 to December 1998, a total of 63,257 Chinese individuals (Hokkien or Cantonese dialect group) aged 45–75 years were recruited. At recruitment, all the study subjects were interviewed in-person by an interviewer with a structured questionnaire. Since April 1994, a total of 28,439 participants donated blood specimens. The study was approved by the Institutional Review Boards of the National University of Singapore and the University of Minnesota, and all study subjects gave written informed consent.

The current study was conducted in a coronary artery diseases (CAD) case-control study nested within SCHS, including 744 incident acute myocardial infarction (AMI) cases and 744 matched controls. Both cases and controls were SCHS participants with donated blood specimens and without a prior history of CAD or stroke at the time of blood collection. The cases selected were incident nonfatal or fatal AMI that occurred during follow-up from blood drawn through December 31, 2010. The controls were alive and free of CAD at the time of the AMI diagnosis or death of the index case. The matching criteria included gender, dialect group (Hokkien, Cantonese), date of birth (±5 years), date of recruitment (±2.5 years), and date of blood collection (±6 months) [20].

Measurement of leukocyte telomere length

DNA of SCHS study subjects was extracted from peripheral blood collected prior to CAD events, using QIAamp DNA Blood kits (Qiagen, Valencia, CA). Relative LTL was measured using a validated monochrome multiplex quantitative PCR (qPCR) method [21]. This method expressed LTL as a ratio (T/S) of telomere repeat length (T) to copy number of a single copy gene albumin (S), relative to a reference sample. The LTL for each sample was measured in duplicates and the average T/S ratio was used for subsequent analysis. Detailed description for LTL measurement in SCHS, including standard curve generation, PCR condition and coefficients of variation was published previously [18].

Measurement of plasma PUFA

Plasma n-3 and n-6 PUFA were quantified from baseline specimens prior to CAD events, in a targeted mode using gas chromatography–mass spectrometry (GC-MS)/MS on an Agilent 7890 GC system (Shanghai, China) equipped with a G7000B QQQ triple quadrupole mass detector and an auto sample injector. Both free and esterified (triglycerides, phospholipids, cholesterol esters) FA fractions were measured in total. Samples were analyzed in 76 batches, with cases and matched controls included in the same batch. Pooled human plasma was used for quality control (QC). The experimental details and the coefficients of variation of the measured FAs were published elsewhere [20].

Genotyping and imputation

Study samples were genotyped on the Illumina HumanOmni ZhongHua-8 Bead Chip. After QC [20, 22,23,24] procedures, 711 cases and 638 controls with complete information for both genotypes and plasma PUFA measurement were included in the current study. Imputation for additional autosomal single nucleotide polymorphisms (SNPs) was performed with IMPUTE2 [25] and genotype calls were based on phase3 1000G cosmopolitan panels.

Statistical method

The main demographic clinical characteristics for the study subjects were compared between CAD cases and controls. Normally distributed quantitative traits, including age, LTL, total plasma n-6 PUFA, linoleic acid (LA) and arachidonic acid (AA), were presented as mean ± SD (standard deviation) and the differences in means between cases and controls were compared by t-test. Non-normally distributed variables, including n6:n3 ratio, total plasma n-3 PUFA, α-linolenic acid (ALA), eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), γ-linolenic acid (GLA) and dihomo-γ-linolenic acid (DGLA) were presented as median with interquartile range, and the differences between groups were determined by the Mann-Whitney U test. Categorical variables, including gender and SNP genotypes, were presented as number of individuals and differences in their frequencies between groups were determined by Pearson’s χ2 test, which was also used for checking significant departure of genotype frequencies from Hardy–Weinberg expectations (HWE). Linear regression was used to investigate the main association of LTL with plasma PUFA and SNP. Cox Proportional-Hazards model was utilized to assess the association of PUFA and LTL with CAD risk, with age, gender and the first three principle components (PCs) included as covariates. Mediation analysis was conducted using the Structural Equation Modeling (SEM) to assess whether the effect of plasma PUFA on CAD risk was mediated through LTL. Non-normally distributed variables were normalized by z-score transformation. Genome-wide interaction analyses were also performed using linear regression by additionally introducing the interaction term (plasma PUFA x SNP) with PUFA and SNP included as covariates in the same regression model. Analysis was first carried out in cases and controls separately and subsequently meta-analyzed using the fixed-effects inverse-variance weighted method. Cochran’s Q test was used to measure heterogeneity and a Qp value cut-off < 0.05 was used to determine SNPs with between-study heterogeneity [26]. The genome-wide interaction analysis was carried out by using an additive model in ProbABEL [27]. Common SNPs with minor allele frequency (MAF) above 3% were included in the current study. All other statistical analyses were carried out using STATA 15.0 (Stata Corp, College station, TX) and a 5% type I error was set to indicate statistical significance (two-tailed) in all analyses.

Results

The main demographic characteristics for the study subjects were presented in Table 1. Cases had significantly lower plasma total n-3 PUFA levels (p = 0.013), EPA levels (p = 0.002) and DHA levels (p = 0.020) as compared to controls. No significant difference was observed between cases and controls for age, gender, LTL, plasma n6:n3 ratio, ALA, total n-6 PUFA and PUFA subtypes.

Table 1 Clinical characteristics of the study subjects

Association between plasma PUFA and LTL

Higher plasma n6:n3 ratio was significantly associated with shorter LTL (T/S ratio) (β = − 0.015, p = 0.018, Table 2). When analyzing the individual effect of plasma n-3 and n-6 PUFA on LTL, only n-3 PUFA showed a significant association and each 1-SD increase in total n-3 PUFA was associated with 0.014 increase in relative LTL (β = 0.014, SE = 0.006, p = 0.024). We further analyzed the association between specific n-3 and n-6 PUFA subtypes with LTL. Both EPA and DHA showed significant associations with LTL while ALA did not. Each 1-SD increase of EPA and DHA was associated with 0.016 (β = 0.016, SE = 0.006, p = 0.011) and 0.015 (β = 0.015, SE = 0.006, p = 0.017) longer relative LTL, respectively (Table 2). The n-6 PUFA subtypes were not associated with LTL (Table 2).

Table 2 Association between plasma PUFA and telomere length in the individual datasets and after meta-analysis

Association between LTL, plasma PUFA and CAD

Higher plasma n6:n3 ratio was significantly associated with increased CAD risk [HR (95%Cl) = 1.114 (1.034, 1.200), P = 0.005, (Table 3)]. When analyzing the individual effect of plasma n-3 and n-6 PUFA on LTL, n-3 PUFA showed a significant protective effect on CAD risk [HR (95%Cl) = 0.885 (0.820, 0.955), P = 0.002] but not n-6 PUFA (Table 3). We further analyzed the association between specific n-3/n-6 PUFA and CAD risk. Both EPA [HR (95%Cl) = 0.884 (0.820, 0.953), P = 0.001] and DHA [HR (95%Cl) = 0.884 (0.819, 0.954), P = 0.002] showed significant association with decreased CAD risk (Table 3). The n-6 PUFA subtypes were not associated with CAD (Table 3). We also observed that longer LTL has protective effect on CAD risk [HR (95%Cl) = 0.664 (0.481, 0.917), P = 0.013, (Table 3)]. Additionally, we evaluated if the effects of PUFA on CAD was mediated by LTL but did not find strong evidence for this in our dataset (Supplemental Table 4).

Table 3 Association between LTL/plasma PUFA and CAD

Interaction between genetic variants and plasma PUFA on LTL

In the assessment of the interaction between plasma PUFAs and genetic variants on LTL, an intergenic SNP, rs529143, was found to modify the effect of plasma n-3 PUFA and DHA on LTL both in CAD cases and controls. After meta-analysis, the interaction reached genome-wide level of significance (Table 4, Supplemental Table 1). Although the main effect of rs529143 on LTL was not significant (p = 0.252, Supplemental Table 2), interaction existed between rs529143 and n-3 PUFA on LTL. Stratification by tertiles of plasma n-3 PUFA levels indicated that individuals carrying the minor C allele have shorter LTL in the lower tertile group while the higher tertile group have longer LTL (Fig. 1). Similar results were observed for the interaction between DHA and rs529143. Minor CC homozygous subjects have shorter LTL in lower plasma DHA tertile group and longer LTL in higher tertile group (Fig. 2).

Table 4 Interaction between genetic variants and plasma PUFA on telomere length
Fig. 1
figure1

The change of LTL by rs529143 within each tertile of plasma n-3 fatty acid level

Fig. 2
figure2

The change of LTL by rs529143 within each tertile of plasma DHA level

We further tested whether rs529143 interacted with dietary intake of PUFAs to affect LTL in all the extended SCHS dataset with complete information for both genotype and diet (N = 21,828) but no significant interaction was detected (Supplemental Table 3).

Discussion

In this prospective nested case-control study of the Singaporean Chinese, we observed an inverse association of plasma n6:n3 ratio with LTL and CAD risk. The association was driven by total plasma n-3 but not n-6 PUFA. When studying the association between specific n-3 PUFA and LTL, higher plasma levels of both EPA and DHA were associated with longer LTL and decreased CAD risk. However, the effects of PUFA and LTL on CAD risks were independent in our study population. We further found a genome-wide interaction between an intergenic variant, rs529143, and n-3 PUFA as well as DHA on LTL. To the best of our knowledge, our study represents the first investigation on the effect of plasma PUFA on LTL and its interaction with genetic variants in a Chinese population.

Studies of the association of PUFA, either dietary or in the plasma, with LTL have largely shown inconsistent results. Most have found telomeric attrition to be attenuated by higher plasma n-3 PUFA levels or increased marine n-3 intake [28, 29], which is consistent with the finding that plasma n-3 PUFA concentration is associated with low proinflammatory markers and high anti-inflammatory markers [30]. In contrast, a large cross-sectional study, comprising the controls of the Nurses’ Health Study found no association between n-3 PUFA and LTL. Instead, the study reported increased n-6 PUFA intake, specifically LA intake, to be inversely associated with [31]. In our study, LTL was significantly associated with plasma n-3 but not n-6 levels. One possible explanation for such discrepancies may be due to the varied dietary intakes (and possibly other lifestyle or environmental factors) between the study populations that may impact on LTL attrition rates. Additionally the ratio of plasma n6:n3 levels has not been evaluated extensively in these previous studies for LTL associations. In a randomized controlled trial, there was no significant differences for LTL changes among groups receiving different n-3 PUFA supplementation. However, an increase of LTL was observed with decreasing of n6:n3 ratio [10]. N-3 and n-6 PUFAs compete for key enzymatic pathways, and thus the relative balance is of health interest [16]. Higher plasma n6:n3 ratio has been associated with higher inflammatory markers, such as TNF-α and IL-6 [32]. Oxidative stress, and inflammation may result in LTL attrition [33]. These data, together with the finding in our study, suggest that rather than just considering the absolute amount of n-3 or n-6 PUFA individually, the background n6:n3 ratio should also be taken into account for clinical studies or for evaluation of nutritional interventions. When we tested the association between specific n-3 FAs and LTL, we observed significant association for EPA and DHA but not ALA. Although ALA can be converted to EPA and DHA, the conversion process is inefficient in humans. A previous study had shown that the same dosages of ALA produced different physiological responses from EPA and DHA to decrease risk factors for metabolic syndrome, while physiological responses to EPA and DHA were similar. This result strongly suggests that ALA exerts its independent effects in metabolic syndrome [34]. A randomized double-blind nutritional intervention study also showed that ALA have different effect on cardiovascular risk markers in healthy elderly subjects compared to EPA and DHA [35].

Previous studies have shown an inverse association between long-chain n-3 PUFAs and CAD risk [36] while adipose tissue AA, a n-6 PUFA, was associated with higher risk of AMI [37, 38]. Similar findings in SCHS between plasma PUFA and CAD has been reported previously [20]. In this SCHS data subset with genetic information, higher plasma n6:n3 ratio was associated with shorter LTL and increased CAD risk. The association was driven mainly by elevated total plasma n-3 but not n-6 PUFA, especially EPA and DHA. Since PUFA and TL are both related to oxidative stress and inflammation, which contribute significantly to the pathogenesis of CAD, we investigated whether the effect of PUFA on CAD is mediated through LTL. However, we did find sufficiently strong evidence for this (Supplemental Table 4) and it may be likely that PUFA and LTL have independent effects on CAD risks.

Our interaction analysis indicated an intergenic SNP, rs529143, could modify the association between n-3 PUFA/DHA and LTL. Carriers of the minor C allele with low n-3 PUFA/DHA (lower tertile) had shorter LTL while those with high n-3 PUFA/DHA (higher tertile) had longer LTL. Regional genes (100 kb) around rs529143 include multiple phospholipase genes such as PLA2G2D and PLA2G2F, which have strong relevance to phospholipid metabolism [39]. Functional annotation of this SNP with expression quantitative trait loci (eQTL) data indicated that rs529143 may affect the expression level of AKR7A3 (p = 4.57 × 10− 6) in transformed fibroblasts [40, 41], which is involved in the detoxification of aldehydes and ketones. The enzymes from the aldo-keto reductases (AKRs) superfamily were also reported to play important roles in nuclear receptor signaling, cellular metabolism, inflammatory responses, endobiotic, osmoregulation and xenobiotic detoxification and hormone synthesis [42, 43]. Moreover, genome-wide yellow fluorescent protein complementation screen has showed that AKR7A3 can interact with DNA-binding transcription factor Ras-related protein 1 (RAP1), one of the core telomeric proteins, to regulate telomeres [44]. The interaction observed in our study might be through the effect of AKR7A3 on telomere length.

Our study has several potential limitations. First, measurements of LTL in our study were mean TL in leukocytes and therefore may not reflect TL dynamics in other tissues [45]. The measurements of TL in vascular cells could be more informative for the mediation analysis for CAD effects [46]. However, there is evidence that within an individual, LTL is likely to be correlated with tissue specific TL [47, 48]. Second, although the association between plasma PUFA levels and LTL was significant in the meta-analysis, when examining the association in cases and controls separately, they were only significant in the latter. Nevertheless the direction of the association was consistent across the datasets and the between-study heterogeneity examined by Cochran’s Q test was not significant (P > 0.05).

Conclusions

We report in this study an inverse association of plasma n6:n3 ratio with LTL and CAD risk and that this association was mainly driven by total plasma n-3 but not n-6 PUFA. Higher plasma levels of both EPA and DHA were associated with longer LTL and decreased CAD risk. We additionally identified an intergenic genetic variant, rs529143 that was observed to modify the association between plasma n-3 PUFA/DHA level and LTL.

Availability of data and materials

All data analyzed during this study are included in this published article and its supplementary information files.

Abbreviations

ALA:

α-Linolenic acid

GLA:

γ-Linolenic acid

AMI:

Acute myocardial infarction

AKR:

Aldo-keto reductase

AA:

Arachidonic acid

CAD:

Coronary artery disease

DGLA:

Dihomo-γ-linolenic acid

DHA:

Docosahexaenoic acid

EPA:

Eicosapentaenoic acid

eQTL:

Expression quantitative trait loci

GC-MS:

Gas chromatography–mass spectrometry

HWE:

Hardy–weinberg expectations

LTL:

Leukocyte telomere length

LA:

Linoleic acid

MS:

Mass spectrometry

MAF:

Minor allele frequency

n6:n3 ratio:

N-6 and n-3 PUFA

n-3:

Omega 3

n-6:

Omega-6

PUFA:

Polyunsaturated fatty acid

PC:

Principle components

QC:

Quality control

qPCR:

Quantitative PCR

RAP1:

Ras-related protein 1

SCHS:

Singapore Chinese health study

SNP:

Single nucleotide polymorphism

SD:

Standard deviation

TL:

Telomere length

References

  1. 1.

    Blackburn EH. Switching and signaling at the telomere. Cell. 2001;106(6):661–73.

    CAS  Article  Google Scholar 

  2. 2.

    Blackburn EH. Telomere states and cell fates. Nature. 2000;408(6808):53.

    CAS  Article  Google Scholar 

  3. 3.

    Blackburn EH. Structure and function of telomeres. Nature. 1991;350(6319):569.

    CAS  Article  Google Scholar 

  4. 4.

    Shammas MA. Telomeres, lifestyle, cancer, and aging. Curr Opin Clin Nutr Metab Care. 2011;14(1):28.

    CAS  Article  Google Scholar 

  5. 5.

    Valdes A, et al. Telomere length in leukocytes correlates with bone mineral density and is shorter in women with osteoporosis. Osteoporos Int. 2007;18(9):1203–10.

    CAS  Article  Google Scholar 

  6. 6.

    Haycock PC, et al. Leucocyte telomere length and risk of cardiovascular disease: systematic review and meta-analysis. BMJ. 2014;349:g4227.

    Article  CAS  Google Scholar 

  7. 7.

    Olovnikov AM. Telomeres, telomerase, and aging: origin of the theory. Exp Gerontol. 1996;31(4):443–8.

    CAS  Article  Google Scholar 

  8. 8.

    Brouilette SW, et al. Telomere length, risk of coronary heart disease, and statin treatment in the west of Scotland primary prevention study: a nested case-control study. Lancet. 2007;369(9556):107–14.

    CAS  Article  Google Scholar 

  9. 9.

    Bekaert S, et al. Telomere length and cardiovascular risk factors in a middle-aged population free of overt cardiovascular disease. Aging Cell. 2007;6(5):639–47.

    CAS  Article  Google Scholar 

  10. 10.

    Kiecolt-Glaser JK, et al. Omega-3 fatty acids, oxidative stress, and leukocyte telomere length: a randomized controlled trial. Brain Behav Immun. 2013;28:16–24.

    CAS  Article  Google Scholar 

  11. 11.

    Von Zglinicki T. Oxidative stress shortens telomeres. Trends Biochem Sci. 2002;27(7):339–44.

    Article  Google Scholar 

  12. 12.

    Demissie S, et al. Insulin resistance, oxidative stress, hypertension, and leukocyte telomere length in men from the Framingham heart study. Aging Cell. 2006;5(4):325–30.

    CAS  Article  Google Scholar 

  13. 13.

    Paul L. Diet, nutrition and telomere length. J Nutr Biochem. 2011;22(10):895–901.

    CAS  Article  Google Scholar 

  14. 14.

    James MJ, Gibson RA, Cleland LG. Dietary polyunsaturated fatty acids and inflammatory mediator production. Am J Clin Nutr. 2000;71(1):343s–8s.

    CAS  Article  Google Scholar 

  15. 15.

    Ramsden CE, et al. Use of dietary linoleic acid for secondary prevention of coronary heart disease and death: evaluation of recovered data from the Sydney diet heart study and updated meta-analysis. BMJ. 2013;346:e8707.

    Article  CAS  Google Scholar 

  16. 16.

    Simopoulos AP. The importance of the omega-6/omega-3 fatty acid ratio in cardiovascular disease and other chronic diseases. Exp Biol Med. 2008;233(6):674–88.

    CAS  Article  Google Scholar 

  17. 17.

    Codd V, et al. Identification of seven loci affecting mean telomere length and their association with disease. Nat Genet. 2013;45(4):422.

    CAS  Article  Google Scholar 

  18. 18.

    Dorajoo R, et al. Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies. Nat Commun. 2019;10(1):2491.

    Article  Google Scholar 

  19. 19.

    Hankin JH, et al. Singapore Chinese health study: development, validation, and calibration of the quantitative food frequency questionnaire. Nutr Cancer. 2001;39(2):187–95.

    CAS  Article  Google Scholar 

  20. 20.

    Sun Y, et al. Plasma fatty acids, oxylipins, and risk of myocardial infarction: the Singapore Chinese health study. J Lipid Res. 2016;57(7):1300–7.

    CAS  Article  Google Scholar 

  21. 21.

    Cawthon RM. Telomere length measurement by a novel monochrome multiplex quantitative PCR method. Nucleic Acids Res. 2009;37(3):e21.

    Article  CAS  Google Scholar 

  22. 22.

    Dorajoo R, et al. A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Genes Nutr. 2015;10(6):1–11.

    CAS  Article  Google Scholar 

  23. 23.

    Chang X, et al. Gene-diet interaction effects on BMI levels in the Singapore Chinese population. Nutr J. 2018;17(1):31.

    Article  CAS  Google Scholar 

  24. 24.

    Han Y, et al. Interaction effects between Paraoxonase 1 variants and cigarette smoking on risk of coronary heart disease in a Singaporean Chinese population. Atherosclerosis. 2015;240(1):40–5.

    CAS  Article  Google Scholar 

  25. 25.

    Marchini J, et al. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet. 2007;39(7):906–13.

    CAS  Article  Google Scholar 

  26. 26.

    Zeggini E, Ioannidis JP. Meta-analysis in genome-wide association studies. Pharmacogenomics. 2009;10(2):191–201.

    Article  Google Scholar 

  27. 27.

    Aulchenko YS, Struchalin MV, van Duijn CM. ProbABEL package for genome-wide association analysis of imputed data. BMC Bioinformatics. 2010;11(1):134.

    Article  CAS  Google Scholar 

  28. 28.

    Farzaneh-Far R, et al. Association of marine omega-3 fatty acid levels with telomeric aging in patients with coronary heart disease. JAMA. 2010;303(3):250–7.

    CAS  Article  Google Scholar 

  29. 29.

    O'Callaghan N, et al. Telomere shortening in elderly individuals with mild cognitive impairment may be attenuated with ω-3 fatty acid supplementation: a randomized controlled pilot study. Nutrition. 2014;30(4):489–91.

    CAS  Article  Google Scholar 

  30. 30.

    Ferrucci L, et al. Relationship of plasma polyunsaturated fatty acids to circulating inflammatory markers. J Clin Endocrinol Metab. 2006;91(2):439–46.

    CAS  Article  Google Scholar 

  31. 31.

    Cassidy A, et al. Associations between diet, lifestyle factors, and telomere length in women. Am J Clin Nutr. 2010;91(5):1273–80.

    CAS  Article  Google Scholar 

  32. 32.

    Kalogeropoulos N, et al. Unsaturated fatty acids are inversely associated and n-6/n-3 ratios are positively related to inflammation and coagulation markers in plasma of apparently healthy adults. Clin Chim Acta. 2010;411(7–8):584–91.

    CAS  Article  Google Scholar 

  33. 33.

    Prasad KN, Wu M, Bondy SC. Telomere shortening during aging: attenuation by antioxidants and anti-inflammatory agents. Mech Ageing Dev. 2017;164:61–6.

    CAS  Article  Google Scholar 

  34. 34.

    Kasielski M, et al. The relationship between peripheral blood mononuclear cells telomere length and diet-unexpected effect of red meat. Nutr J. 2015;15(1):68.

    Article  CAS  Google Scholar 

  35. 35.

    Lee TM, et al. A pontine region is a neural correlate of the human affective processing network. EBioMedicine. 2015;2(11):1799–805.

    Article  Google Scholar 

  36. 36.

    Mozaffarian D, Rimm EB. Fish intake, contaminants, and human health: evaluating the risks and the benefits. JAMA. 2006;296(15):1885–99.

    CAS  Article  Google Scholar 

  37. 37.

    Baylin A, Campos H. Arachidonic acid in adipose tissue is associated with nonfatal acute myocardial infarction in the central valley of Costa Rica. J Nutr. 2004;134(11):3095–9.

    CAS  Article  Google Scholar 

  38. 38.

    Kark JD, et al. Adipose tissue n− 6 fatty acids and acute myocardial infarction in a population consuming a diet high in polyunsaturated fatty acids. Am J Clin Nutr. 2003;77(4):796–802.

    CAS  Article  Google Scholar 

  39. 39.

    Murakami M, et al. The roles of the secreted phospholipase A(2) gene family in immunology. Adv Immunol. 2016;132:91–134.

  40. 40.

    Watanabe K, et al. Functional mapping and annotation of genetic associations with FUMA. Nat Commun. 2017;8(1):1826.

    Article  CAS  Google Scholar 

  41. 41.

    Fretts AM, et al. Processed meat, but not unprocessed red meat, is inversely associated with leukocyte telomere length in the strong heart family study. J Nutr. 2016;146(10):2013–8.

    CAS  Article  Google Scholar 

  42. 42.

    Jin Y, Penning TM. Aldo-keto reductases and bioactivation/detoxication. Annu Rev Pharmacol Toxicol. 2007;47:263–92.

    CAS  Article  Google Scholar 

  43. 43.

    Chow RKK, et al. AKR7A3 suppresses tumorigenicity and chemoresistance in hepatocellular carcinoma through attenuation of ERK, c-Jun and NF-κB signaling pathways. Oncotarget. 2017;8(48):83469.

    Article  Google Scholar 

  44. 44.

    Lee O-H, et al. Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells. Mol Cell Proteomics. 2011;10(2):M110 001628.

    Google Scholar 

  45. 45.

    Soares-Miranda L, et al. Physical activity, physical fitness and leukocyte telomere length: the cardiovascular health study. Med Sci Sports Exerc. 2015;47(12):2525.

    Article  Google Scholar 

  46. 46.

    Madrid AS, et al. Short telomere length and ischemic heart disease: observational and genetic studies in 290 022 individuals. Clin Chem. 2016;62(8):1140–9.

    CAS  Article  Google Scholar 

  47. 47.

    Wilson WRW, et al. Blood leucocyte telomere DNA content predicts vascular telomere DNA content in humans with and without vascular disease. Eur Heart J. 2008;29(21):2689–94.

    CAS  Article  Google Scholar 

  48. 48.

    Okuda K, et al. Telomere length in the newborn. Pediatr Res. 2002;52(3):377.

    Article  Google Scholar 

Download references

Acknowledgements

We thank Siew-Hong Low of the National University of Singapore for supervising the field work of the Singapore Chinese Health Study and the Ministry of Health in Singapore for assistance with the identification of AMI cases via database linkages. We also acknowledge the founding, longstanding principal investigator of the Singapore Chinese Health Study, Mimi C. Yu.

Funding

The Singapore Chinese Health Study was supported by grants from the National Medical Research Council, Singapore (NMRC/CIRG/1456/2016), and the National Institutes of Health (R01 CA144034 and UM1 CA182876).

Author information

Affiliations

Authors

Contributions

CKH, YF, WPK and JMY conceptualized and designed the studies as the principal investigators of the study cohorts; XC, RD, YS and LW collated, analyzed and interpreted the data; CCK and JJL performed genotyping and its quality control, CNO generated the fatty acid data; XC and RD drafted the manuscript and all authors contributed to its critical revision for important intellectual content and gave final approval its submission.

Corresponding authors

Correspondence to Yechiel Friedlander or Chew-Kiat Heng.

Ethics declarations

Ethics approval and consent to participate

The Singapore Chinese Health Study was approved by the Institutional Review Boards of the National University of Singapore and the University of Minnesota, and all study subjects gave written informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare no conflict of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1: Table S1.

Interaction between genetic variants and plasma PUFA on telomeres in SCHS_CAD cases and controls. Table S2. Association between genetic variant and telomeres. Table S3. The mediation effect of telomeres on the association between plasma PUFA and coronary artery disease. Table S4. Interaction between genetic variants and PUFA intake on telomeres in SCHS (N = 21,828)

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Chang, X., Dorajoo, R., Sun, Y. et al. Effect of plasma polyunsaturated fatty acid levels on leukocyte telomere lengths in the Singaporean Chinese population. Nutr J 19, 119 (2020). https://doi.org/10.1186/s12937-020-00626-9

Download citation

Keywords

  • Polyunsaturated fatty acid
  • Leukocyte telomere length
  • Gene-diet interaction