Abstract
Grip strength is an important biomarker reflecting muscle strength, and depression is a psychiatric disorder all over the world. Several studies found a significant inverse association between grip strength and depression, and there is also evidence for common physiological mechanisms between them. We used twin data from Qingdao, China to calculate genetic correlations, and we performed a bivariate GWAS to explore potential SNPs, genes, and pathways in common between grip strength and depression. 139 pairs of Dizygotic twins were used for bivariate GWAS. VEAGSE2 and PASCAL software were used for gene-based analysis and pathway enrichment analysis, respectively. And the resulting SNPs were subjected to eQTL analysis and pleiotropy analysis. The genetic correlation coefficient between grip strength and depression was -0.41 (-0.96, -0.15). In SNP-based analysis, 7 SNPs exceeded the genome-wide significance level (P<5×10−8) and a total of 336 SNPs reached the level of suggestive significance (P<1×10−5). Gene-based analysis and pathway-based analysis identified genes and pathways related to muscle strength and the nervous system. The results of eQTL analysis were mainly enriched in tissues such as the brain, thyroid, and skeletal muscle. Pleiotropy analysis shows that 9 of the 15 top SNPs were associated with both grip strength and depression. In conclusion, this bivariate GWAS identified potentially common pleiotropic SNPs, genes, and pathways in grip strength and depression.
Introduction
Grip strength, which can reflect muscle strength to some extent [1] and is correlated with nutritional status [2], disease status, and all-cause mortality [3], is a very important biomarker of aging [4]. Depression is a common psychiatric disorder that can significantly decrease the quality of life of older adults [5], leading to a heavy burden of disease worldwide [6]. Several previous cross-sectional [7, 8] and cohort [9, 10] studies have found a significant inverse association between grip strength and depression, and there is also evidence for common physiological mechanisms between grip strength and depression. For example, the muscle can release inflammatory cytokines such as IL-6, IL-8, and IL-15 [11]. Some studies have shown that weak skeletal muscle strength is related to an increase in serum proinflammatory cytokines [12, 13], which can lead to depression [14]. Furthermore, lower grip strength and depression have been shown to be associated with shortened cellular telomere length [15, 16]. In addition, physical activity can have a positive effect on serotonin [17], dopamine [18], and norepinephrine levels [19], which are closely related to depression.
In addition to environmental factors, genetic factors also play a very important role in the relationship between grip strength and depression. An elderly twin study found a heritability of 35% for hand-grip strength [20]. In the twin study by Tian et al., handgrip strength was found to have a moderate heritability of 59.68% [21]. The results of one meta-analysis showed a heritability of 56% (95% CI: 0.46–0.67) for isometric grip strength [22]. A large twin study in Sri Lanka found that the heritability of broadly defined depression was 61% in women [23]. Through a meta-analysis of twin studies, the heritability of depression was found to range from 31% to 48% [24]. However, there are no studies on the genetic correlation of grip strength with depression.
To date, little is known about shared genetic variation in depression and grip strength. Some overlapping results were found between depression and grip strength by contrasting univariate studies. Two cohort studies in older Swedish adults found that the APOEε4 allele was simultaneously associated with decreased grip strength and depression [25, 26]. In addition, serval studies have shown that the vitamin D receptor (VDR) gene is associated with muscle strength and senile depression symptoms [27–29]. The results of these univariate studies indirectly support the existence of common susceptibility genes for grip strength and depression, but there is still a lack of direct evidence. Compared with univariate research, a bivariate genome-wide association study (GWAS) can add two variables to the model simultaneously to find the potential pleiotropic genetic variation between phenotypes. Bivariate GWASs have higher statistical ability and more accurate parameter estimation than univariate studies [30, 31]. In addition, twin samples are more effective for studies targeting complex phenotypes than general population samples [32].
In summary, we hypothesized that grip strength and depression are regulated by common genetic factors. Therefore, we used twin data from Qingdao, China to calculate genetic correlations, and we performed a bivariate GWAS to explore potential single nucleotide polymorphisms (SNPs), genes, and pathways in common between grip strength and depression.
Methods
Study population
We used a twin sample from the Qingdao Twin Registration System in China, and the details of the sample can be found in previous literature [33]. Blood was collected from participants in a fasted state, and zygosity was determined by sex, blood type, and microsatellite DNA gene scanning with typing techniques. Participants differing in sex or blood type were identified as dizygotic (DZ) twins. Monozygotic (MZ) twins were identified when both sex and blood type was the same and all 15 short tandem repeats (STRs) were concordant. Twins fulfilling the following criteria could be included in the study: 1) older than 18 years; 2) available for follow-up; and 3) had blood samples, questionnaires, and phenotypic measurement data. We excluded twins if they 1) were pregnant or lactating; 2) were missing key indicator information; 3) had a critical illness or were unable to complete the survey; or 4) were professional athletes. Ultimately, 235 MZ and 134 DZ twins were included in the study.
Phenotypes
Information such as sex and age were collected by questionnaires. The 30-item Geriatric Depression Scale (GDS-30, Chinese version) was used to assess depressive symptoms. The scale consists of 30 questions with a total score ranging from 0–30, with higher scores representing more severe depressive symptoms. This scale has been adapted precisely for the assessment of depression in middle-aged and older adults, and it is appropriate for the Chinese population [34]. Physical examinations were performed by trained investigators. Participants were required to squeeze the grip of the handgrip dynamometer (WCS-100, Nantong, China) as strongly as they could, with each hand tested 3 times. Like some other studies [35, 36], the maximum value was taken as the grip strength for analysis.
Genetic correlations
We used Mx software to construct a bivariate Cholesky decomposition model. The classical twin model decomposes the total phenotypic variation into additive genetic effect (A), common environment effect (C), and special environment effect (E). The likelihood ratio chi-square test was used to compare the difference between the full model and its nested model. If a P value greater than 0.05 indicated that the full model was not significantly different from its nested model, the nested model was selected according to the Akaike information criterion (AIC) and the minimalist principle.
Genotyping, quality control, and imputation
We used Infinium Omni2.5Exome-8v1.2 BeadChip from Illumina for genotyping DZ twins. The chip covers a wide range and has a good typing detection rate. After typing detection, SNPs were first quality-controlled, and individual SNPs should meet: 1) Locus missing rate < 0.05 (SNPs with high missing rates were difficult to genotype); 2) Calling rate > 0.98 (The low calling rate reflects the poor quality of the sample); 3) Hardy-Weinberg equilibrium (HWE) > 1×10−6 (HWE is a tool for tagging SNPs with a large number of genotyping errors); 4) Minor allele frequency (MAF) >0.05 (Variants with very low MAF are more susceptible to genotyping errors, as the rarer alleles occur in only a few individuals.). Then, the quality-controlled SNPs were imputed with the use of IMPUTE2 software [37], based on linkage disequilibrium (LD) principles with data from the third phase of the 1000 Genomes Project (ASIAN) [38] as the reference. The SNPs were quality controlled again after imputation with the standards of 1) a Hardy-Weinberg equilibrium (HWE)>1×10−6; 2) a minor allele frequency (MAF)>0.05; 3) information contents (info> = 0.9). Finally, 7,165,663 SNPs were used in the bivariate GWAS.
Bivariate GWAS
SNP-based analysis
To explore the association of SNPs in handgrip-depression pairs, we used genome-wide efficient mixed-model association (GEMMA) [39], adjusting for sex, age, and BMI. Rank transformation based on Blom’s formula was used to normalize the skewed distributions of handgrip strength and depression. GEMMA fitted a multivariate linear mixed model (mvLMM) while controlling for relatedness and population structure to test marker associations of handgrip strength with depression. The significance level was defined as a P value<5×10−8 as a conventional Bonferroni-corrected threshold [40]. The suggested level of association was a P value<1×10−5, a commonly utilized threshold in GWASs [41]. The quantile-quantile (Q-Q) plot was used to visualize the population stratification, and the Manhattan plot was used to visualize the P value for each SNP on each chromosome.
Gene-based analysis
Versatile Gene-based Association Study-2 (VEGAS2) software [42] was used for gene-based analysis with the “1000G East ASIAN Population” as a reference. A total of 21,221 genes were tested so that the Bonferroni-corrected significance threshold was a P value<2.36×10−6(0.05/21,221). The nominal significance level was a P value<0.05 [43].
Pathway enrichment analysis
Pathway Scoring Algorithm (PASCAL) software [44] was used to evaluate pathway scores for pathway enrichment analysis. First, SNP loci were located in genes, and the association scores of all genes in a pathway were calculated. The chi-square and empirical scores were used to evaluate high-scoring pathways. Then, we obtained access information from the KEGG, BioCarta, and Reactome databases.
Expression quantitative trait locus (eQTL) analysis
For the top 60 SNPs that reached the suggested level of significance, we examined their functionality using data from the GTEx portal (version 8) [45]. A P value<0.05 was considered significant in the single-tissue eQTL analysis. The posterior probability m-value that the eQTL effect existed in each tissue of a cross-tissue meta-analysis higher than 0.9 indicated that the tissue having had an eQTL effect [46].
Pleiotropy analysis
We performed genetic pleiotropy tests on the top 15 SNPs that were most significant before imputation using the R package “pleio”, thus verifying whether they were indeed associated with both grip strength and depression.
Ethics statement
This study conformed to the declaration of Helsinki, and all participants provided written informed consent. This study was approved by the Regional Ethics Committee of the Qingdao Center for Disease Control. And the decision reference number was 2012–01.
Results
Basic characteristics
The basic characteristics of the twin are shown in Table 1. A total of 369 pairs of twins were enrolled in this study. Among them, 134 were DZ twins and 235 were MZ twins. There were 362 males and 376 females. In the total sample, the median (interquartile range) age was 50 (45, 57), and the median (interquartile range) grip strength and depression scores of participants were 30.4 (23.8, 40.2) and 7 (4, 11), respectively. In the DZ twin sample, the median (interquartile range) age was 49 (45, 56), and the median (interquartile range) grip strength and depression scores of the participants were 31.1 (25.2, 42.5) and 7 (4, 11), respectively.
Table 1. Characteristics of participants by sex.
| Variables | Male | Female | Total population | ||||
|---|---|---|---|---|---|---|---|
| N | M (Q) | N | M (Q) | N | M (Q) | ||
| Total sample | Age (year) | 362 | 50 (45, 58) | 376 | 50 (46, 56) | 738 | 50 (45, 57) |
| Grip strength | 362 | 40.8 (34.8, 47.7) | 376 | 24.4 (21.3, 27.7) | 738 | 30.4 (23.8, 40.2) | |
| Depression score | 362 | 7 (3.75, 11) | 376 | 7 (4, 10) | 738 | 7 (4, 11) | |
| DZ twins | Age (year) | 138 | 49 (45, 57) | 130 | 49 (45, 56) | 268 | 49 (45, 56) |
| Grip strength | 138 | 42 (36.9, 49.9) | 130 | 25.2 (22.2, 28.6) | 268 | 31.1 (25.2, 42.5) | |
| Depression score | 138 | 7 (3, 11) | 130 | 6 (4, 10) | 268 | 7 (4, 11) | |
M: median; Q: quartile.
Genetic correlations
As shown in Table 2, the phenotypic correlation coefficient between grip strength and depression was -0.27 (P<0.001), and the best fitting Cholesky decomposition model (ACE) identified that the genetic correlation coefficient between the two phenotypes was -0.41 (-0.96, -0.15). This finding suggested a moderate genetic correlation between grip strength and depression. The common and special environmental correlation coefficients were insignificant.
Table 2. Genetic correlations between grip strength and depression.
| Phenotypic | Model | rG (95%CI) | rC (95%CI) | rE (95%CI) | Phenotypic correlation coefficient | -2LL | Δdf | χ2 | P |
|---|---|---|---|---|---|---|---|---|---|
| Grip strength–depression | ACE | -0.41 (-0.96, -0.15) | -1.00 (-1.00, 1.00) | -0.04 (-0.17, 0.09) | -0.27 (-0.34, -0.19) | 3610.99 | |||
| AE | -1.00 (-1.00, -0.78) | - | -0.12 (-0.23, -0.01) | -0.24 (-0.31, -0.16) | 3618.14 | 1 | 7.153 | 0.007 |
rG: genetic correlation coefficient; rC: common environmental correlation coefficient; rE: special environmental correlation coefficient; -2LL: double negative logarithmic likehood function value; df: free degree.
Bivariate GWAS
SNP-based analysis
A bivariate GWAS was performed in 134 DZ twin pairs. As shown in the Q-Q plot (Fig 1) for the bivariate measures of grip strength and depression, the inflation coefficients for the groups had a λ value of 1.027, indicating no stratification of the population. The Manhattan plot (Fig 2) provides a visualization of the results of the GWAS. As shown in the plot, 7 SNPs exceeded the genome-wide significance level (P<5×10−8) and a total of 336 SNPs reached the level of suggestive significance (P<1×10−5). The most significant SNP was rs118190698 (P = 1.35×10−9) located in the RAB27B gene on chromosome 18; followed by rs79530590 (P = 1.50×10−9), located in the LOC107985152 gene; rs117744620 (P = 3.31×10−9) located in the LRR1 gene; rs117546604 (P = 3.84×10−9), rs150220336 (P = 4.39×10−8), and rs147079354 (P = 4.62×10−8), located in the ME2 gene; and rs79287957 (P = 4.62×10−8) located close to the LINC02871 gene. The top 60 SNPs are shown in Table 3 sorted by P value.
Fig 1. Quantile-quantile plot for bivariate genome-wide association study of grip strength and depression.
The horizontal axis represents the expected -log10 (P), while the vertical axis represents the observed -log10 (P). The red line represents the expectation of the null hypothesis of no association, and the gray shaded area represents 95% confidence intervals of the null hypothesis. The black dots represent the observed data, and λ indicates genomic inflation.
Fig 2. Manhattan plot for bivariate genome-wide association study of grip strength and depression.
The horizontal axis represents autosomes and the X chromosome, while the vertical axis represents the P-values of SNPs. The red line represents the genome-wide significance threshold (5×10−8), and the lower horizontal dashed line represents the suggestive significance level (1×10−5).
Table 3. Top 60 SNPs that reached P < 1×10−5 from bivariate GWAS of grip strength and depression.
| SNP | Chr | Band | BP | P-value | Gene/Nearest gene |
|---|---|---|---|---|---|
| rs118190698 | 18 | q21.2 | 52480259 | 1.35E-09 | RAB27B |
| rs79530590 | 18 | q21.2 | 48520209 | 1.50E-09 | LOC107985152 |
| rs117744620 | 14 | q21.3 | 50079611 | 3.31E-09 | LRR1 |
| rs117546604 | 18 | q21.2 | 48472778 | 3.84E-09 | ME2 |
| rs150220336 | 18 | q21.2 | 48388016 | 4.39E-08 | ME2 |
| rs147079354 | 18 | q21.2 | 48447754 | 4.62E-08 | ME2 |
| rs79287957 | 20 | p12.2 | 11048805 | 4.92E-08 | LINC02871 |
| rs75534602 | 7 | p12.1 | 50634883 | 6.13E-08 | DDC |
| rs117533783 | 7 | p12.2 | 50525408 | 7.82E-08 | DDC |
| rs116994552 | 8 | p21.1 | 28076758 | 8.16E-08 | LOC100131127 |
| rs11973477 | 7 | q32.3 | 130908819 | 1.01E-07 | MKLN1 |
| rs6961574 | 7 | q32.3 | 130908776 | 1.04E-07 | MKLN1 |
| rs149538842 | 3 | p12.3 | 76440134 | 1.06E-07 | ROBO2 |
| rs78161270 | 7 | p12.2 | 50541930 | 1.13E-07 | DDC |
| rs117549429 | 21 | q22.13 | 38971496 | 1.53E-07 | KCNJ6 |
| rs74214322 | 7 | p13 | 45401720 | 3.00E-07 | ELK1P1 |
| rs118025410 | 5 | q13.2 | 68859027 | 3.08E-07 | GTF2H2C |
| rs76553625 | 5 | q12.3 | 64268965 | 3.19E-07 | CWC27 |
| rs5773363 | 1 | p35.2 | 31918631 | 3.24E-07 | SERINC2 |
| rs12657552 | 5 | p13 | 68855113 | 3.29E-07 | GTF2H2C |
| rs4081993 | 5 | p13 | 68856116 | 3.33E-07 | GTF2H2C |
| rs147869550 | 15 | q23 | 71596350 | 4.45E-07 | THSD4 |
| rs1868887 | 7 | p12.2 | 50479856 | 4.76E-07 | IKZF1 |
| rs79147986 | 5 | p15.1 | 15593286 | 5.05E-07 | FBXL7 |
| rs201380943 | 11 | p11.2 | 47778625 | 5.41E-07 | FNBP4 |
| rs116890548 | 12 | q24.31 | 121620387 | 5.43E-07 | P2RX7 |
| rs573505577 | 11 | p15.1 | 19918670 | 5.48E-07 | NAV2 |
| rs80251137 | 7 | q36.3 | 155920157 | 6.09E-07 | LOC105375601 |
| rs2995920 | 4 | p14.3 | 37904456 | 6.24E-07 | TBC1D1 |
| rs141475535 | 1 | q44 | 244427543 | 7.24E-07 | LOC105373262 |
| rs116961485 | 8 | q13.1 | 66227114 | 7.79E-07 | PPIAP86 |
| rs534143679 | 3 | p22.3 | 32433754 | 7.96E-07 | CMTM7 |
| rs62358249 | 5 | q14.3 | 84421657 | 8.02E-07 | RBBP4P6 |
| rs17008263 | 1 | q41 | 220877255 | 8.02E-07 | C1orf115 |
| rs11851625 | 14 | q12 | 30314159 | 8.15E-07 | PRKD1 |
| rs12563371 | 1 | p21.1 | 103499755 | 8.22E-07 | COL11A1 |
| rs200867673 | 7 | p14.3 | 32871494 | 8.88E-07 | DPY19L1P2 |
| rs2297807 | 20 | q13.33 | 62575853 | 8.90E-07 | UCKL1 |
| rs57042988 | 7 | q31.2 | 114791544 | 9.16E-07 | LINC01392 |
| rs10914394 | 1 | p35.2 | 31915692 | 9.18E-07 | LOC105378625 |
| rs181979988 | 4 | p14.3 | 38496704 | 9.38E-07 | LINC01258 |
| rs141325897 | 1 | p21.1 | 103598274 | 9.38E-07 | COL11A1 |
| rs57244134 | 12 | q22.13 | 94661218 | 9.93E-07 | CEP83 |
| rs10914386 | 1 | p35.2 | 31909072 | 1.06E-06 | SERINC2 |
| rs10914387 | 1 | p35.2 | 31909124 | 1.06E-06 | SERINC2 |
| rs6702129 | 1 | p35.2 | 31910482 | 1.06E-06 | SERINC2 |
| rs1320586 | 1 | p35.2 | 31908201 | 1.07E-06 | SERINC2 |
| rs12122438 | 1 | p35.2 | 31909448 | 1.07E-06 | SERINC2 |
| rs12141959 | 1 | p35.2 | 31909380 | 1.07E-06 | SERINC2 |
| rs6690908 | 1 | p35.2 | 31910089 | 1.07E-06 | SERINC2 |
| rs6675883 | 1 | p35.2 | 31910202 | 1.07E-06 | SERINC2 |
| rs6688664 | 1 | p35.2 | 31910337 | 1.07E-06 | SERINC2 |
| rs139995350 | 1 | p35.2 | 31910430 | 1.07E-06 | SERINC2 |
| rs6691338 | 1 | p35.2 | 31910655 | 1.07E-06 | SERINC2 |
| rs75429043 | 14 | q12 | 30316306 | 1.13E-06 | PRKD1 |
| rs11795332 | 9 | p22.3 | 15352410 | 1.13E-06 | RPL7P33 |
| rs113400337 | 9 | p22.3 | 15360062 | 1.13E-06 | RPL7P33 |
| rs377290438 | 6 | q12 | 68889736 | 1.14E-06 | LINC02549 |
| rs12323862 | 14 | q12 | 30317951 | 1.14E-06 | PRKD1 |
| rs79219406 | 9 | p22.3 | 15347617 | 1.18E-06 | RPL7P33 |
SNP, nucleotide polymorphism; Chr, chromosome; BP, base pair.
Gene-based analysis
In the gene-based analysis, 2 genes reached a significant association level (P = 2.36×10−6): GTF2H2C_2 (P = 3.08×10−7) and GTF2H2C (P = 3.08×10−7). Furthermore, 1,262 genes reached the nominal significance level (P<0.05). The top 60 genes are shown in S1 Table, and most of these genes were related to the nervous system, actin, and immune system.
Pathway enrichment analysis
In the pathway enrichment analysis, we identified 621 biological pathways associated with grip strength and depression (emp-P<0.05). We ranked the top 60 pathways by the strength of association in S2 Table. Most of these pathways were involved in hormone synthesis, the immune system, and the nervous system.
eQTL analysis
The eQTL analysis across tissues using the Asian population as a reference found that 13 SNPs were significant eQTLs in several tissues, including brain tissues, skeletal muscle, the tibial nerve, and the thyroid (S3 Table; S1–S3 Figs). Among them, the rs10914394 (S1 Fig, Brain–Spinal cord (cervical c-1), P value = 5.2×10−5, m-value = 1.00; Muscle–Skeletal, P value = 4.3×10−28, m-value = 1.00; Nerve–Tibial, P value = 7.2×10−13, m-value = 1.00; Thyroid, P value = 4.3×10−12, m-value = 1.00), rs10914386 (S2 Fig, Brain–Spinal cord (cervical c-1), P value = 1.4×10−4, m-value = 1.00; Muscle–Skeletal, P value = 1.3×10−28, m-value = 1.00; Nerve–Tibial, P value = 3.2×10−13, m-value = 1.00; Thyroid, P value = 1.3×10−11, m-value = 1.00), and rs10914387 (S3 Fig, Brain–Spinal cord (cervical c-1), P value = 1.4×10−4, m-value = 1.00; Muscle–Skeletal, P value = 2.5×10−28, m-value = 1.00; Nerve–Tibial, P value = 3.1×10−13, m-value = 1.00; Thyroid, P value = 7.2×10−12, m-value = 1.00) SNPs were significantly associated with the expression of the SERINC2 gene in brain tissues and muscle tissues.
Pleiotropy analysis
Table 4 shows the results of the pleiotropy analysis. In the top 15 SNPs, 9 were associated with both grip strength and depression. In addition, rs117549429 was associated with depression only, and rs79287957, rs75534602, rs117533783, rs149538842, and rs78161270 were associated with grip strength only.
Table 4. The results of pleiotropy analysis for bivariate GWAS of grip strength-depression identified top 15 SNPs.
| SNP | Chr | BP | P-value a | Trait of nonzero β b | P for test0 c | P for test1 d | Associated trait |
|---|---|---|---|---|---|---|---|
| rs118190698 | 18 | 52480259 | 1.35E-09 | G; D | 1.88E-06 | 2.25E-04 | G; D |
| rs79530590 | 18 | 48520209 | 1.50E-09 | G; D | 5.52E-06 | 2.09E-03 | G; D |
| rs117744620 | 14 | 50079611 | 3.31E-09 | G; D | 1.11E-07 | 7.75E-03 | G; D |
| rs117546604 | 18 | 48472778 | 3.84E-09 | G; D | 1.70E-06 | 4.19E-04 | G; D |
| rs150220336 | 18 | 48388016 | 4.39E-08 | G; D | 9.39E-07 | 1.77E-04 | G; D |
| rs147079354 | 18 | 48447754 | 4.62E-08 | G; D | 1.00E-06 | 1.66E-04 | G; D |
| rs79287957 | 20 | 11048805 | 4.92E-08 | G | 3.10E-05 | 5.61E-01 | G |
| rs75534602 | 7 | 50634883 | 6.13E-08 | G | 3.56E-05 | 2.45E-01 | G |
| rs117533783 | 7 | 50525408 | 7.82E-08 | G | 2.10E-05 | 9.59E-02 | G |
| rs116994552 | 8 | 28076758 | 8.16E-08 | G; D | 1.03E-06 | 2.48E-02 | G; D |
| rs11973477 | 7 | 130908819 | 1.01E-07 | G; D | 2.03E-06 | 1.06E-03 | G; D |
| rs6961574 | 7 | 130908776 | 1.04E-07 | G; D | 1.97E-06 | 1.03E-03 | G; D |
| rs149538842 | 3 | 76440134 | 1.06E-07 | G | 5.63E-06 | 2.60E-01 | G |
| rs78161270 | 7 | 50541930 | 1.13E-07 | G | 2.86E-06 | 1.20E-01 | G |
| rs117549429 | 21 | 38971496 | 1.53E-07 | D | 1.87E-02 | 5.90E-02 | D |
SNP, nucleotide polymorphism; Chr, chromosome; BP, base pair; G, grip strength; D, depression.
a The P-value was derived from bivariate GWAS.
b Sequential tests of pleiotropy with a P threshold of 0.05.
c Single test of the number of traits associated with genotype, H0 (test0): all betas = 0.
d Single test of the number of traits associated with genotype, H0 (test1): one or less beta is nonzero.
Discussion
A total of 369 pairs of twins were included in this study. The genetic correlation between grip strength and depression was evaluated by a bivariate genetic model. It was found that there was a moderate genetic correlation between grip strength and depression, and the genetic correlation coefficient was -0.41 (-0.96, -0.15), suggesting that there was a common genetic basis between them. At present, most of the studies on the heritability of grip strength and depression are carried out for a single variable. Previous studies have shown that the heritability of grip strength and depression is high, but there is still a gap in the research in determining their common genetic correlation coefficient.
Then, a bivariate GWAS was carried out in 134 pairs of DZ twins to identify the common SNPs, genes, and pathways of grip strength and depression. In the SNP-based analysis, rs117744620, located in the LRR1 gene on chromosome 14, exceeded the genome-wide significance level. LRR1 encodes a protein with a leucine-rich repeat. A previous study showed that LRR1 regulates 4-1BB-mediated signaling cascades, which activate NF-кB [47], and NF-кB could affect depression. LRR1 can also affect actin [48], thereby affecting muscle strength. Three SNPs (rs117546604, rs150220336, rs147079354) located in or near the ME2 gene also exceeded the genome-wide significance level. The ME2 gene encodes a mitochondrial NAD-dependent malic enzyme. ME2 has been shown to be associated with generalized epilepsy [49], suggesting that ME2 may affect both the nervous system and muscle strength. In addition, ME2 has been found to be associated with susceptibility to psychosis and mania [50], and the knockdown of ME2 may affect PI3K/AKT signaling [51], all suggesting that ME2 is also associated with depression.
In the top 60 SNPs that reached the suggested level of association, three SNPs (rs75534602, rs117533783, rs78161270) were located near the DDC gene. A study has shown that the DDC gene is associated with postpartum anxiety [52]. In addition, the DDC gene was also associated with aromatic L-amino acid decarboxylase deficiency (AADCD), a neurotransmitter metabolism disorder in the mainland Chinese population, the main symptoms of which include early-onset hypotonia [53]. Therefore, the DDC gene may affect grip strength and depression simultaneously. rs116890548 is located in the P2RX7 gene on chromosome 12. P2RX7 is associated with the inflammatory response and neuroimmune mechanisms of depression and neurodegenerative diseases [54, 55]. This gene can also affect calcium channels [56, 57] and is associated with bone and joint diseases [58]. Therefore, P2RX7 may affect muscle strength. Moreover, three SNPs (rs11851625, rs75429043, rs12323862) were located in the PRKD1 gene on chromosome 14. The PRKD1 gene can regulate actin [59] and affect skeletal muscle [60]. The PRKD1 gene is also associated with neurons [61], NF-кB [62], and the inflammatory response [63]. Therefore, PRKD1 may also regulate depression and muscle strength simultaneously.
In gene-based analysis, we found 2 genes that exhibited a significant association, GTF2H2C_2 and GTF2H2C. However, there are too few studies on these two genes, and we cannot yet explain the relationship of these two genes with the phenotype. Furthermore, among the genes with nominal significance levels, many were associated with grip strength and depression: (1) FNBP1 can affect neuronal dendrites [64] and actin [65], which may affect grip strength and depression; (2) MOG is associated with multiple sclerosis [66, 67], the main symptoms of which include depression and decreased muscle strength; (3) the SACS gene can affect motor and sensory neuropathy [68], and is associated with complex neurological disorders [69]; (4) the KMO gene is associated with depression [70, 71] and Huntington’s disease [72], the symptoms of which include muscle atrophy; (5) the TECPR2 gene is tightly linked to the nervous system [73–76] and may influence depression and grip strength by affecting nerves; and (6) MGTA5 can affect the severity of multiple sclerosis [77, 78]. MGTA5 may also be associated with attempted suicide [79], and therefore may be associated with depression. In addition, the expression levels of KCNN4 [80, 81], MOG [82, 83], and SNHG12 [84, 85] genes can influence inflammatory factors, which may affect grip strength and depression by influencing the inflammatory response.
In the pathway enrichment analysis, many pathways were related to hormone synthesis and neural signal transduction. (1) Androgen biosynthesis, steroid hormones, and steroid hormone biosynthesis are related to androgen synthesis and metabolism. Androgen levels are not only associated with depression but also affect grip strength [86, 87]. (2) Potassium channels and the nervous system can regulate the resting membrane potential in neurons, and it can affect both depression and muscle strength [88, 89]. (3) Signaling by RHO GTPases can affect guanine nucleotides, and studies have shown that RHO GTPases can affect actin [90] and neuronal development [91, 92], thereby affecting muscle strength and depression. (4) The phospholipase C mediated cascade, activated point mutants of FGFR2, and FGFR ligand binding and activation are related to fibroblast growth factor receptor. Fibroblast growth factors are associated with skeletal muscle development [93], and a study has found that fibroblast growth factor-2 can affect depression [94]. (5) Cytokine receptor interaction pathway can affect cytokines. Cytokines are soluble extracellular proteins or glycoproteins that are crucial intercellular regulators and mobilizers of cells engaged in innate as well as adaptive inflammatory host defenses. This pathway may affect grip strength and depression by influencing the inflammatory response.
The current research has several strengths. First, this is the first genetic correlation and bivariate GWAS on grip strength and depression, which will help to study the common genetic basis of these phenotypes. Second, our study was conducted in a twin sample, which is more effective when exploring complex phenotypes such as depression [32]. In addition, we performed a pleiotropic analysis, and the results showed that a number of the SNPs we obtained were indeed associated with both grip strength and depression, which further confirmed the accuracy of our study. At the same time, our research has some limitations. First, because it is difficult to recruit twin samples, our sample size was relatively small, which limited our ability to find more potential SNPs, genes, and pathways. Smaller sample sizes may also lead to lower power, but we have used pleiotropy analysis to improve the credibility of the results. Second, we cannot fully explain the SNP, gene, and pathway associations that we found. For example, although two genes exceeded the Bonferroni-corrected significance threshold and the same genes have also been found in univariate GWASs, we cannot explain the associated biological mechanism. Third, because our sample included both middle-aged and older adults, and the depression questionnaire we used was the GDS-30, this may have had an impact on the assessment of depressive symptoms.
Conclusion
In conclusion, this bivariate GWAS identified potentially common pleiotropic SNPs, genes, and pathways in grip strength and depression. However, more in-depth studies are still needed to validate our results.
Supporting information
(DOCX)
(DOCX)
(DOCX)
NES is the normalized effect size (β) from single-tissue eQTL analysis. P-value is from the t-test that compares observed NES in single-tissue eQTL analysis to the null hypothesis of no NES. m-value represents a posterior probability that the effect of eQTL exists in each tissue of a cross-tissue meta-analysis.
(TIF)
NES is the normalized effect size (β) from single-tissue eQTL analysis. P-value is from the t-test that compares observed NES in single-tissue eQTL analysis to the null hypothesis of no NES. m-value represents a posterior probability that the effect of eQTL exists in each tissue of a cross-tissue meta-analysis.
(TIF)
NES is the normalized effect size (β) from single-tissue eQTL analysis. P-value is from the t-test that compares observed NES in single-tissue eQTL analysis to the null hypothesis of no NES. m-value represents a posterior probability that the effect of eQTL exists in each tissue of a cross-tissue meta-analysis.
(TIF)
Acknowledgments
We thank Dr. Gu Zhu for his technical guidance in data analysis. And we thank all participants and contributors of Qingdao Twins.
Data Availability
All SNPs datasets of this study are available from the the European Variation Archive (EVA) (Accession No. PRJEB23749).
Funding Statement
This study was supported by the grants from the National Natural Science Foundation of China (82073641). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
(DOCX)
(DOCX)
(DOCX)
NES is the normalized effect size (β) from single-tissue eQTL analysis. P-value is from the t-test that compares observed NES in single-tissue eQTL analysis to the null hypothesis of no NES. m-value represents a posterior probability that the effect of eQTL exists in each tissue of a cross-tissue meta-analysis.
(TIF)
NES is the normalized effect size (β) from single-tissue eQTL analysis. P-value is from the t-test that compares observed NES in single-tissue eQTL analysis to the null hypothesis of no NES. m-value represents a posterior probability that the effect of eQTL exists in each tissue of a cross-tissue meta-analysis.
(TIF)
NES is the normalized effect size (β) from single-tissue eQTL analysis. P-value is from the t-test that compares observed NES in single-tissue eQTL analysis to the null hypothesis of no NES. m-value represents a posterior probability that the effect of eQTL exists in each tissue of a cross-tissue meta-analysis.
(TIF)
Data Availability Statement
All SNPs datasets of this study are available from the the European Variation Archive (EVA) (Accession No. PRJEB23749).