Article | Open | Published:

# Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort

## Abstract

Unraveling the complexity of aging is crucial for understanding its mechanisms and its role as a risk factor for most chronic conditions. Advancements marked by genome-wide association studies (GWASs) have sparked interest in gene cataloguing in the context of aging and age-related conditions. Here, we used GWAS to explore whether single nucleotide polymorphisms (SNPs) were associated with functional and anthropometric parameters in a cohort of old community-dwellers enrolled in the ilSIRENTE study. Analyses were carried out in men and women aged 80+ years enrolled in the ilSIRENTE study (n = 286) and replicated in the inCHIANTI study (n = 1055). Genotyping was accomplished on Infinium Human610-QUAD version 1. In the ilSIRENTE population, genetic variants in ZNF295 and C2CD2 (rs928874 and rs1788355) on chromosome 21q22.3, were significantly associated with the 4-meter gait speed (rs928874, p = 5.61 × 10−8; rs1788355, p = 5.73 × 10−8). This association was not replicated in the inCHIANTI population. Our findings suggest that specific SNPs may be associated with a key measure of physical performance in older adults. GWASs using larger samples are needed to confirm these preliminary results to enhance our comprehension of complex age-associated phenomena.

## Introduction

Advancements in healthcare, nutrition and sanitation have remarkably extended the average human life expectancy. Thus, the elderly population has expanded considerably in Western countries. One of the most notable consequences of this demographic shift is the increased prevalence of chronic degenerative diseases and functional impairments. In such a scenario, the promotion of strategies aimed at preserving physical function and preventing its deterioration toward disability is crucial for the sustainability of healthcare systems1,2. Unfortunately, little is known about the mechanisms by which aging increases susceptibility to chronic diseases and disability, which hampers the identification of suitable therapeutic targets.

It is traditionally assumed that successful aging results from the combination of genetic and environmental factors3. Genome-wide association studies (GWASs) have been proposed as a valuable strategy for identifying genetic variants associated with positive or negative health phenotypes, such as longevity and age-related diseases4,5,6. For instance, GWASs allowed for the identification of polymorphisms associated with top five leading causes of death in adulthood and advanced age (i.e., heart disease, cancer, stroke, Alzheimer’s disease, and diabetes)7,8,9,10,11.

The importance of unraveling disease-associated gene variants resides in their possible exploitation for treatment purposes. For example, the discovery of the genes responsible for maturity-onset diabetes of the young (MODY, which is considered to be a form of progeria)12 has allowed for selecting patients whose glycemia is better controlled on sulphonylureas than insulin13.

Several age-related phenotypes (e.g., pulmonary function, fasting glucose, bone mineral density, cognitive function) show moderate to high heritability14,15,16. In addition, genetic background has been proposed to contribute up to approximately 65% of the variability in muscle mass and strength17,18. GWASs have subsequently identified specific single-nucleotide polymorphisms (SNPs) associated with muscle mass, strength and physical function in late life (reviewed by19). In particular, SNPs pertaining to angiotensin-converting enzyme (ACE) gene I/D, α-actinin-3 (ACTN3) R577X, and myostatin (MSTN) K153R have been extensively studied19. With the exception of MSTN K153R, which seems to be associated with a sarcopenic phenotype in very old women20, no conclusive findings have been obtained for other candidate genetic variants19.

The present study was therefore undertaken to identify specific genetic variants associated with measures of functional status, physical performance, muscle mass, muscle strength, and cognition in a well-characterized and genetically homogeneous cohort of octogenarians and nonagenarians living in a mountain community in Central Italy, enrolled in the ilSIRENTE study (“Invecchiamento e Longevità nel Sirente”)21. The longitudinal design of the study enabled us to explore whether specific SNPs were associated with changes in the variables of interest over time.

## Results

DNA was purified from 286 participants. Age and gender distribution as well as anthropometric and functional characteristics were unvaried between the subset under investigation and the enrollees from whom DNA was unavailable (data not shown). The main characteristics of the subsample used for the present study are shown in Table 1 along with those of the inCHIANTI (“Invecchiare in Chianti”) replication population22.

Manhattan plots, QQ plots and top hits list [summary statistics for the single-nucleotide polymorphisms (SNPs) showing p-values < 10−5] were generated for the analyses of association between genetic data and activities of daily living (ADL) score23, calf circumference (CC)24, mid-arm muscle circumference (MAMC)24, handgrip strength, 4-meter walk test, Short Physical Performance Battery (SPPB) summary score25, Cognitive Performance Scale (CPS) score26, as well as for changes in SPPB and 4-meter walk test over two years (Figs 19).

In the Manhattan plots, genome-wide significant SNPs are color-coded in red (p values < 5 × 10−8), whilst those displayed in orange showed p values < 10−5 >5 × 10−8. The genomic inflation factor (lambda) for each GWAS analysis, ranging from 0.985 to 1.072, is shown in the QQ plots (Figs19). We identified a single association peak that exceeded the Bonferroni’s threshold for significance (Fig.7). This peak was detected in chromosome 21q22.3 in the analysis of 4-meter gait speed (rs928874, p = 5.61 × 10−8; rs1788355, p value = 5.73 × 10−8), located within a non-coding exon at the start of the ZNF295 gene and the intergenic region upstream the same gene. The association signal was located in a 95-kb block of linkage disequilibrium that contains two genes: ZNF295 and C2CD2. To further test the association of this region with the 4-meter walk speed, we analyzed rs928874 in an independent replication dataset obtained from the inCHIANTI cohort. Rs928874 failed to reach significance in participants either over 80 years (n = 184, p = 0.51) or over 65 years (n = 871, p = 0.294).

## Discussion

In high-income countries, the proportion of people aged over 60 years is growing faster than any other age group, as a result of both longer life expectancy and declining fertility rates. Although population aging can be seen as a success story for public health policies and socioeconomic development, it also implies that chronic age-related diseases and functional impairment have emerged as a major challenge in the 21st century27. In such a scenario, a deeper understanding of the biology of aging may provide fundamental insights into the pathogenesis of age-associated conditions, such as declining physical performance, dementia, diabetes, cardiovascular disease and cancer28.

The determinants of aging and longevity are not completely known; yet, genetics are thought to play a significant role in successful aging29. The development of efficient, affordable, high-density SNP genotyping technologies has provided the opportunity to undertake GWASs to screen large numbers of samples for genetic variations associated with positive or negative health phenotypes30. In particular, the possibility of identifying genetic variants associated with skeletal muscle phenotypes in older people has inspired several studies as the decline in muscle mass and strength (i.e., sarcopenia) is a major contributing factor to negative outcomes in late life.

In the present work, we present the results of a GWAS of aging phenotypes in a cohort of old and very old community-living persons enrolled in the ilSIRENTE study. This cohort is ideal for research on aging because the population has been thoroughly characterized through the collection of comprehensive information over a long follow-up21. Furthermore, the genetically homogeneous nature of this region facilitates the identification of possible genetic variants. For the present investigation, analyses were designed to identify SNPs associated with quantitative aging phenotypes, focused on functional status, physical performance, anthropometry, and cognition (i.e., ADL score, CC, MAMC, handgrip strength, SPPB summary score, 4-meter walk test, and CPS score). We also sought to determine if specific genetic variants were associated with changes in the SPPB summary score and 4-meter gait speed over two years. A single association peak in chromosome 21q22.3 was found with 4-meter gait speed test (rs928874, p = 5.61 × 10−8; rs1788355, p = 5.73 × 10−8; Fig. 7). Within this locus falls the ZNF295 gene that encodes a zinc finger protein implicated in transcriptional regulation. This same locus was previously linked with handgrip strength in middle-aged and older adults enrolled in the Hunter Community Study31. Remarkably, the 21q22.3 region belongs to a group of newly-identified loci associated with age-related diseases, including diabetes mellitus, neurodegeneration, cancer, and cardiovascular disease32. SNPs in these loci fall within regulatory regions that modulate the expression of nearby genes32.

The association between rs928874 found in our cohort and 4-meter walk speed was not confirmed in the InCHIANTI population either in participants over 80 years (n = 184, p = 0.51) or 65–80-year-old enrollees (n = 871, p = 0.294). One possible explanation for such a discrepancy may reside in differences in the linkage disequilibrium levels of rs928874 between the two cohorts33. Differences in participant testing procedures and in the covariates used for adjusting the analyses might provide an additional explanation for the lack of concordance between the two populations. On the other hand, we cannot rule out the possibility that the sample size was insufficient for capturing low-frequency variants as well as polymorphisms associated with subtle effects. In such a context, meta-analytical approaches may be able to provide a more comprehensive screening of low-frequency genetic variants associated with aging and capture their pleiotropic effects32. Yet, a recent meta-analysis of gait speed GWASs conducted in 31,478 older adults from 17 cohorts of the CHARGE consortium did not find any genome-wide significant signals34.

It should be considered that complex age-related phenotypes, such as those investigated in the present work, are influenced by a wealth of biological pathways involving multiple genes. The individual effects of SNPs may therefore be expected to be very small and difficult to identify. To further complicate the matter, the impact of genetic factors is likely modulated by social and environmental factors or may be mediated by some other endophenotypes, including inflammation32,35. As such, the association of genetic variants with certain phenotypes may be environment-specific and therefore hardly replicable across cohorts36,37. In this respect, it is worth noting that education, the prevalence of certain disease conditions, circulating levels of tumor necrosis factor-alpha (TNF-α), and physical performance were dissimilar between the two cohorts under study (Table 1).

In order to accurately evaluate the staging of biological age and related clinical conditions, as well as the rates of decline of strength and function, the participants from ilSIRENTE study underwent evaluations at several time points. As a result, the generation of longitudinal trajectories of biological variables together with age-related outcomes (cardiovascular diseases, dementia, fractures, etc.), and genetic variants associated with aging may help identify factors amenable to interventions aimed at improving the quality of life of older adults. In particular, the existence of SNPs linked with physical performance suggests the intriguing possibility of identifying individuals at risk of functional impairment at an early stage, therefore allowing for interventions to be implemented in a timely manner. The accomplishment of this challenging task requires ad hoc designed studies to conclusively establish if specific genetic variants are indeed associated with relevant aging phenotypes and identify the biological networks governing such complex traits.

## Methods

### Study population

The ilSIRENTE study is a prospective cohort study conducted in the mountain community living in the Sirente geographic area (L’Aquila, Abruzzo) in Central Italy (GPS coordinates: 42.349918, 13.399544). The study was designed by the Department of Geriatrics, Neurosciences and Orthopedics of the Catholic University of the Sacred Heart (Rome, Italy) and developed by the teaching nursing home “Opera Santa Maria della Pace” (Fontecchio, L’Aquila, Italy), in a partnership with local administrators and primary care physicians of Sirente Mountain Community Municipalities.

The ilSIRENTE study protocol is detailed elsewhere 21. Briefly, a preliminary list of persons living in the Sirente area was obtained at the end of October 2003 from the Registry Offices of the 13 municipalities involved in the study. Potential participants were identified by selecting all persons born in the Sirente area before January 1st 1924 and living locally at the time of the survey. Among the eligible persons (n = 429), the refusal rate was very low (16%). Age and gender distribution were not different between people who refused to participate and the enrollees. The overall sample population enrolled in the ilSIRENTE study consisted of 364 persons. For the study we considered 286 participants for whom blood sample for DNA extraction was available. The study protocol was approved by the Catholic University’s Ethics Committee. All methods were performed in accordance with the relevant guidelines and regulations and an informed consent was obtained from all participants or from their relatives in the case of cognitive impairment 21.

### Clinical assessment, anthropometry and functional testing

The Minimum Data Set for Home Care (MDS-HC) form was administered to all participants 26 to collect data on 350 parameters including socio-economic variables, physical and cognitive status, and major clinical diagnoses.

Muscle mass was estimated from CC and MAMC using a non-elastic flexible plastic tape, as detailed previously 24. CC was measured on the left leg (or the right leg for left-handed persons) in a sitting position with the knee and ankle at a right angle and feet resting on the floor. CC was taken at the point of greatest circumference, without compressing subcutaneous tissues. MAMC was calculated using the standard formula 38:

$${\rm{M}}{\rm{A}}{\rm{M}}{\rm{C}}={\rm{m}}{\rm{i}}{\rm{d}}-{\rm{a}}{\rm{r}}{\rm{m}}\,{\rm{c}}{\rm{i}}{\rm{r}}{\rm{c}}{\rm{u}}{\rm{m}}{\rm{f}}{\rm{e}}{\rm{r}}{\rm{e}}{\rm{n}}{\rm{c}}{\rm{e}}\,-\,(3.14\times {\rm{t}}{\rm{r}}{\rm{i}}{\rm{c}}{\rm{e}}{\rm{p}}{\rm{s}}\,{\rm{s}}{\rm{k}}{\rm{i}}{\rm{n}}{\rm{f}}{\rm{o}}{\rm{l}}{\rm{d}}\,{\rm{t}}{\rm{h}}{\rm{i}}{\rm{c}}{\rm{k}}{\rm{n}}{\rm{e}}{\rm{s}}{\rm{s}})$$

The measurement of triceps skinfold thickness was obtained using a Harpenden Skinfold Caliper. All measurements were taken on the right arm unless conditions were present that could interfere with the assessment (e.g., amputation, lymphedema, neurological diseases, recent upper extremity fracture, severe osteoarthritis with functional limitation).

Physical performance was assessed via the SPPB25, as previously described39. Briefly, the SPPB is composed of three timed subtests that evaluate standing balance, usual gait speed over a short track, and the ability to rise from a chair. For the standing balance test, participants were asked to stand in three increasingly challenging positions for 10 s each: standing with feet in side-by-side, semi-tandem, and full tandem positions. For the gait speed subtest, participants were asked to walk at their usual pace along a 4-m course, starting from a standing still position. The faster of two trials (m·s−1) was used for the calculation of the summary score. Finally, for the chair-stand subtest, participants were asked to rise from a chair and sit down five times as quickly as possible with arms folded across the chest. Each of the three SPPB subtasks was categorized into a five-level score according to predefined cut-points25, with 0 representing inability to do the test and 4 corresponding to the highest level of performance.

Upper extremity muscle strength was quantified using a hand-held hydraulic dynamometer (North Coast Medical, Morgan Hill, CA). As previously described40, participants performed one familiarization trial and one measurement trial with each hand, and the result from the stronger side was used for the analyses. Cognitive status was assessed using the six-item CPS26. CPS was scored on a 7-point ordinal scale, with higher scores indicative of worse cognitive performance.

Additional information about family history, lifestyle, physical activity and other behavioral factors was collected using questionnaires adopted in the inCHIANTI study22.

### Blood sample collection, genotyping and data processing

Fasting blood samples were obtained by venipuncture of the median cubital vein, using commercial collection tubes. Samples were processed for routine hematological and clinical chemistry tests. A whole-blood aliquot was frozen within 2 hrs of collection and kept at −80 °C until DNA extraction. Samples were thawed on ice and mixed thoroughly before use. Genomic DNA was extracted from peripheral blood according to standard procedures. Genotyping was performed in the extracted DNA for 561,490 SNPs on Infinium Human 610-QUAD version 1 (Illumina, CA, USA), according to the manufacturer’s protocol.

Analyses were limited to the 547,937 autosomal SNPs. We applied standard quality control procedures to the data, namely exclusion of samples with SNP call rates of less than 95%, samples with non-European ancestry, or samples demonstrating relatedness defined as identity-by-descent proportion of inheritance (pi_hat from the PLINK software toolset version 1.07 greater than 0.15)41, SNPs with minor allele frequency (MAF) less than 0.01, and SNPs with a Hardy-Weinberg equilibrium p value less than 0.001. The cryptic relatedness threshold led to the exclusion of individuals who shared more than 15% of their genome, which meant that related individuals down to third or fourth degree relatives were not included in the final analysis. The index individual whose sample had the best call rate from each related pair was selected for inclusion.

SNPs were then imputed to the June 2010 release of the 1,000 genomes project haplotypes using MaCH software (version 1.0)42. All SNPs passing quality control of MAF >0.05 and imputation quality from MaCH at >0.30 were included in the GWAS analyses. Genome-wide significance threshold was set at 5.0 × 10−8.

### Statistical analysis

Each genotyped and imputed SNP that passed quality control metrics was tested for genetic association with the following measurements using linear regression modeling: (1) ADL score (age, gender, number of diseases were included as covariates in the model); (2) MAMC (age, gender, number of diseases as covariates); (3) CC (age, gender, number of diseases as covariates); (4) SPPB summary score (age, gender, pain, number of diseases as covariates); (5) 4-meter walk test (age, gender, pain, number of diseases as covariates); (6) handgrip strength (age, gender, number of diseases as covariates); and (7) CPS (age, gender, number of diseases, depression, dementia as covariates).

In order to leverage the longitudinal nature of the ilSIRENTE dataset, we also analyzed changes over two years in (1) 4-meter walk test (age, gender, pain, number of diseases as covariates), (2) SPPB score (age, gender, pain, number of diseases as covariates), and (3) CPS (age, gender, number of diseases, depression, dementia as covariates). To avoid floor effect, individuals who scored 0 on the SPPB or who were unable to complete the 4-meter walk test at baseline were excluded. Each phenotype was transformed using quantile normalization to account for the non-normal distribution of some traits.

### Replication

The results of the genotyping analysis obtained from the ilSIRENTE cohort were compared with those of an existing genome-wide dataset generated for the InCHIANTI study43. The latter, similar to ilSIRENTE, is a study on the factors contributing to the decline in mobility and cognition in late life in two towns located in the Tuscany countryside (Italy)22. Genotype data were available for 184 persons over 80 years of age and 871 between 65 and 80 years.

### Data availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

## References

1. 1.

Cesari, M. et al. The geriatric management of frailty as paradigm of “The end of the disease era”. Eur. J. Intern. Med. 31, 11–14 (2016).

2. 2.

Mander, T. Longevity and healthy ageing - Will healthcare be drowned by the grey Tsunami or sunk by the demographic iceberg? Post. Reprod. Health. 20, 8–10 (2014).

3. 3.

Eaton, N. R. et al. Genes, environments, personality, and successful aging: toward a comprehensive developmental model in later life. J. Gerontol. A Biol. Sci. Med. Sci. 67, 480–488 (2012).

4. 4.

Karasik, D. & Newman, A. Models to explore genetics of human aging. Adv. Exp. Med. Biol. 847, 141–161 (2015).

5. 5.

Murabito, J. M., Yuan, R. & Lunetta, K. L. The search for longevity and healthy aging genes: insights from epidemiological studies and samples of long-lived individuals. J. Gerontol. A Biol. Sci. Med. Sci. 67, 470–479 (2012).

6. 6.

Erikson, G. A. et al. Whole-Genome Sequencing of a Healthy Aging Cohort. Cell. 165, 1002–1011 (2016).

7. 7.

Klein, R. J. et al. Complement factor H polymorphism in age-related macular degeneration. Science. 308, 385–389 (2005).

8. 8.

Grant, S. F. et al. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat. Genet. 38, 320–323 (2006).

9. 9.

CARDIoGRAMplusC4D Consortium et al. Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25–33 (2013).

10. 10.

Lambert, J. C. et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease. Nat. Genet. 45, 1452–1458 (2013).

11. 11.

Kilarski, L. L. et al. Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12. Neurology. 83, 678–685 (2014).

12. 12.

Martin, G. M. Genes, rates of aging, and duration of human life. Am. J. Med. 117, 882–883 (2004).

13. 13.

Hattersley, A. T. & Pearson, E. R. Minireview: pharmacogenetics and beyond: the interaction of therapeutic response, beta-cell physiology, and genetics in diabetes. Endocrinology. 147, 2657–2663 (2006).

14. 14.

Karasik, D., Demissie, S., Cupples, L. A. & Kiel, D. P. Disentangling the genetic determinants of human aging: biological age as an alternative to the use of survival measures. J. Gerontol. A Biol. Sci. Med. Sci. 60, 574–587 (2005).

15. 15.

Wilk, J. B. et al. Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study. Hum. Mol. Genet. 12, 2745–2751 (2003).

16. 16.

Mathias, R. A. et al. Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data. BMC Genet. 4(Suppl 1), S36 (2003).

17. 17.

Abney, M., McPeek, M. S. & Ober, C. Broad and narrow heritabilities of quantitative traits in a founder population. Am. J. Hum. Genet. 68, 1302–1307 (2001).

18. 18.

Reed, T., Fabsitz, R. R., Selby, J. V. & Carmelli, D. Genetic influences and grip strength norms in the NHLBI twin study males aged 59–69. Ann. Hum. Biol. 18, 425–432 (1991).

19. 19.

Garatachea, N. & Lucía, A. Genes and the ageing muscle: a review on genetic association studies. Age (Dordr). 35, 207–233 (2013).

20. 20.

González-Freire, M. et al. The K153R variant in the myostatin gene and sarcopenia at the end of the human lifespan. Age (Dordr) 32, 405–409 (2010).

21. 21.

Landi, F. et al. The ilSIRENTE study: a prospective cohort study on persons aged 80 years and older living in a mountain community of Central Italy. Aging Clin. Exp. Res. 17, 486–493 (2005).

22. 22.

Ferrucci, L. et al. Subsystems contributing to the decline in ability to walk: bridging the gap between epidemiology and geriatric practice in the InCHIANTI study. J. Am. Geriatr. Soc. 48, 1618–1625 (2000).

23. 23.

Katz, S., Downs, T. D., Cash, H. R. & Grotz, R. C. Progress in development of the index of ADL. Gerontologist 10, 20–30 (1970).

24. 24.

Landi, F. et al. Age-related variations of muscle mass, strength, and physical performance in community-dwellers: results from the Milan EXPO survey. J. Am. Med. Dir. Assoc. 18, 88.e17–88.e24 (2017).

25. 25.

Guralnik, J. M. et al. A short physical performance battery assessing lower extremity function: association with self-reported disability and prediction of mortality and nursing home admission. J. Gerontol. 49, M85–94 (1994).

26. 26.

Morris, J. N. et al. Comprehensive clinical assessment in community setting: applicability of the MDS-HC. J. Am. Geriatr. Soc. 45, 1017–1024 (1997).

27. 27.

Marzetti, E. et al. Brand new medicine for an older society. J. Am. Med. Dir. Assoc. 17, 558–559 (2016).

28. 28.

Cesari, M. et al. The geriatric management of frailty as paradigm of “The end of the disease era”. Eur. J. Intern. Med. 31, 11–14 (2016).

29. 29.

Pilling, L. C. et al. Genomics and successful aging: grounds for renewed optimism? J. Gerontol. A Biol. Sci. Med. Sci. 67, 511–519 (2012).

30. 30.

Stranger, B. E., Stahl, E. A. & Raj, T. Progress and promise of genome-wide association studies for human complex trait genetics. Genetics. 187, 367–383 (2011).

31. 31.

Karasik, D. et al. Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study. J. Bone Miner. Res. 17, 1718–1727 (2002).

32. 32.

He, L. et al. Pleiotropic meta-analyses of longitudinal studies discover novel genetic variants associated with age-related diseases. Front. Genet. 7, 179 (2016).

33. 33.

Yashin, A. I. Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures. Front Genet. 7, 188 (2016).

34. 34.

Ben-Avraham, D. et al. The complex genetics of gait speed: genome-wide meta-analysis approach. Aging (Albany NY). 9, 209–246 (2017).

35. 35.

Kalliolias, G. D. & Ivashkiv, L. B. TNF biology, pathogenic mechanisms and emerging therapeutic strategies. Nat. Rev. Rheumatol. 12, 49–62 (2016).

36. 36.

Kulminski, A. M. et al. Birth cohort, age, and sex strongly modulate effects of lipid risk alleles identified in genome-wide association studies. PLoS One 10, e0136319, https://doi.org/10.1371/journal.pone.0136319 (2015).

37. 37.

Bae, H. T. et al. Genome-wide association study of personality traits in the long life family study. Front. Genet. 4, 65 (2013).

38. 38.

Antonelli Incalzi, R. et al. Nutritional assessment: a primary component of multidimensional geriatric assessment in the acute care setting. J. Am. Geriatr. Soc. 44, 166–174 (1996).

39. 39.

Calvani, R. et al. Systemic inflammation, body composition, and physical performance in old community-dwellers. J. Cachexia Sarcopenia Muscle; https://doi.org/10.1002/jcsm.12134 (2016).

40. 40.

Landi, F. et al. Impact of physical function impairment and multimorbidity on mortality among community-living older persons with sarcopaenia: results from the ilSIRENTE prospective cohort study. BMJ Open. 6, e008281, https://doi.org/10.1136/bmjopen-2015-008281 (2016).

41. 41.

Purcell, S. et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559–575 (2007).

42. 42.

Li, Y., Willer, C. J., Ding, J., Scheet, P. & Abecasis, G. R. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet. Epidemiol. 34, 816–834 (2010).

43. 43.

Melzer, D. et al. A genome-wide association study identifies protein quantitative trait loci (pQTLs). PLoS Genet. 4, e1000072, https://doi.org/10.1371/journal.pgen.1000072 (2008).

## Acknowledgements

This work was supported by the Intramural Research Programs of the NIH, National Institute on Aging (Z01-AG000949–02), the Innovative Medicines Initiative – Joint Undertaking (IMI-JU #115621), intramural research grants from the Catholic University of the Sacred Heart (D3.2 2013 and D3.2 2015), Fondazione Roma (NCDs Call for Proposals 2013), and the nonprofit research foundation “Centro Studi Achille e Linda Lorenzon”. Additional funding was obtained from Microsoft Research. The ilSIRENTE study was supported by a grant from the “Comunità Montana Sirentina” (Secinaro, L’Aquila, Italy).

## Author information

### Affiliations

1. #### Microsoft Research, Los Angeles, California, USA

• David Heckerman
2. #### Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, 35 Convent Drive, Room 1A-1000, Bethesda, MD, 20892, USA

• Bryan J. Traynor
3. #### Center for Geriatric Medicine (CEMI), Department of Geriatrics, Neurosciences and Orthopedics, Catholic University of Sacred Heart, Rome, 00168, Italy

• Anna Picca
• , Riccardo Calvani
• , Emanuele Marzetti
•  & Francesco Landi
4. #### Genomics Technology Group, Laboratory of Neurogenetics, National Institute on Aging, 35 Convent Drive, Room 1A-1000, Bethesda, MD, 20892, USA

• Dena Hernandez
•  & Sampath Arepali
5. #### Molecular Genetics Unit, Laboratory of Neurogenetics, National Institute on Aging, 35 Convent Drive, Room 1A-1000, Bethesda, MD, 20892, USA

• Michael Nalls
6. #### Longitudinal Studies Section, Clinical Research Branch, National Institute on Aging, 251 Bayview Blvd., Room BRC/04C225, Baltimore, MD, 21224, USA

• Luigi Ferrucci

### Contributions

D.H., A.P., and R.C. conceived and designed the study, B.J.T. performed genotyping analysis, D.F., M.N., and S.A. analyzed the data, E.M. contributed to the study design and drafted the manuscript, L.F. and F.L. provided supervision and revised the manuscript.

### Competing Interests

E.M., R.C., and F.L. are partners of the SPRINTT Consortium, which is partly funded by the European Federation of Pharmaceutical Industries and Associations (EFPIA). The other authors declare no conflict of interest.

### Corresponding author

Correspondence to Francesco Landi.

### DOI

https://doi.org/10.1038/s41598-017-13475-0